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Anushree, U and Shenoy, Revathi P and Hebbar, Shrikiran and Bhat, Vinutha R and Bakkannavar, Shankar M and Prabhu, Krishnananda (2017) Hydrocarbon poisoning in a child - A cause of hypoxia and seizure: Case report. Advanced Science Letters, 23 (3). pp. 1967-1968. ISSN 1936-6612

Girisha, KM and Hebbar, Malavika and Shukla, Anju and Shah, Hitesh and Nismath, Shifa (2017) Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia. Journal of Human Genetics, 62 (3). pp. 437-441. ISSN 1434-5161

Bhat, Ramesh Y (2017) Platelet indices in neonatal sepsis: A review. World Journal of Clinical Infectious Diseases, 7 (1). pp. 6-10.

Girisha, KM (2017) Down syndrome in diverse populations. American Journal Of Medical Genetics : Part A, 173A (1). pp. 42-53.

Girisha, KM (2017) The novel EDAR p.L397H missense mutation causes autosomal dominant hypohidrotic ectodermal dysplasia. Journal of the European Academy of Dermatology and Venereology, 31 (1). e17 -e20. ISSN 0926-9959

Salian, Smrithi and Gandham, SriLakshmi Bhavani and Shukla, Anju and Girisha, KM (2017) Additional Three Patients With Smith-McCort Dysplasia Due to Novel RAB33B Mutations. American Journal of Medical Genetics- Part A, 173 (3). pp. 1-8. ISSN 1552-4825

Nayak, Krishnananda and Kumar, Pratap and Shetty, Ranjan K and Shetty, Kiran and Jyothi, * and Lewis, Leslie and Mayya, Shreemathi S (2017) Altered Arterial Doppler Flow Pattern And Perinatal Outcome In Intrauterine Growth Restriction. Asian Journal of Pharmaceutical and Clinical Research, 10 (3). pp. 425-428. ISSN 0974-2441

Renu, G and Pai, Mamatha S and Nayak, Baby S and Mundkur, Suneel C and Nayak, Dinesh M and Shashidhara, YN and George, Anice (2017) Effectiveness of Home Safety Supervisory Program (HSSP) on Childhood Injury, Caregivers’ Knowledge and Behavioural Outcomes- A Randomized Controlled Trial Protocol. Medico-Legal Update, 17 (1). pp. 124-129. ISSN 0971-720X

Girisha, KM and Shukla, Anju (2017) Mutations in EBF3 disturb transcriptional profiles and cause intellectual disability, ataxia, and facial dysmorphism. The American Journal of Human Genetics, 100 (1). pp. 117-127. ISSN 0002-9297

Ravi, Rohit and Gunjawate, Dhanshree R and Yerraguntla, Krishna and Lewis, Leslie and Rajashekhar, B (2017) A National Survey of Knowledge, Attitude and Practices among Pediatricians towards Newborn Hearing Screening in India. International Journal of Pediatric Otorhinolaryngology, 95. pp. 9-14. ISSN 0165- 5876

Renu, G and George, Anice and Nayak, Baby S and Pai, Mamatha S and Mundkur, Suneel C and Nayak, Dinesh M and Shashidhara, YN (2017) A Portrayal of Childhood Injury among Under-Five Year Children. Indian Journal of Public Health Research & Development, 8 (1). pp. 24-28. ISSN 0976-0245

Shetty, Ranjitha S and Kamath, Veena G and Nayak, Dinesh M and Hegde, Asha (2017) Rotavirus associated acute gastroenteritis among under-five children admitted in two secondary care hospitals in southern Karnataka, India. Clinical Epidemiology and Global Health, 5 (1). pp. 28-32. ISSN 2213-3984

Aroor, Shrikiran and Mundkur, Suneel C and Kanaparthi, Shravan and Kumar, Sandeep (2017) Waldmann’s Disease (Primary Intestinal Lymphangiectasia) with Atrial Septal Defect. Journal of Clinical and Diagnostic Research, 11 (4). pp. 3-4. ISSN 0973-709X

Girisha, KM (2016) Glycosaminoglycan levels in dried blood spots of patients with mucopolysaccharidoses and mucolipidoses. Molecular Genetics and Metabolism, 120 (3). pp. 247-254. ISSN 1096-7192

Bhavani, Gandham SriLakshmi and Girisha, KM (2016) Spectrum of SMPD1 mutations in Asian-Indian patients with acid sphingomyelinase (ASM)-deficient Niemann–Pick disease. American Journal of Medical Genetics Part-A, 170 (10). pp. 2719-2730.

Hebbar, Malavika and Shukla, Anju and Girisha, KM (2016) Homozygous deletion of Exons 2 and 3 of NPC2 associated with Niemann–Pick disease type C. American Journal of Medical Genetics Part A, 170 (9). pp. 2486-2489.

Girisha, KM and Shah, Hitesh and Bhavani, Gandham SriLakshmi (2016) A novel multiple joint dislocation syndrome associated with a homozygous nonsense variant in the EXOC6B gene. European Journal of Human Genetics, 24 (8). pp. 1206-1210.

Upadhyay, Neha and Pai, Muralidhar V and Nayak, Shalini S and Girisha, KM and Shukla, Anju (2016) Congenital omphalocele and cleft palate in two fetuses. Congenital Anomalies, 56 (4). pp. 190-191. ISSN 0914-3505

Khurana, Sonia and Rao, Bhamini K and Lewis, Leslie and Bhat, Ramesh Y and Jayashree, Purkayastha and Kamath, Asha and Kumaran, Senthil D (2016) Development and validation of educational leaflet for caregivers of preterm infants. Journal of Clinical and Diagnostic Research, 10 (7). YC01-YC04. ISSN 0973-709X

Shah, Krupa H and Nayak, Shalini S and Shukla, Anju and Girisha, KM (2016) Spectrum of urorectal septum malformation sequence. Congenital Anomalies, 56 (4). pp. 119-126. ISSN 0914-3505

Girisha, KM (2016) Cortical-Bone Fragility — Insights from sFRP4 deficiency in Pyle’s disease. New England Journal of Medicine, 374 (26). pp. 2553-2. ISSN 0028-4793

Girisha, KM (2016) A Novel EDARADD 5 -Splice site mutation resulting in activation of two alternate cryptic 5-Splice sites causes autosomal recessive hypohidrotic ectodermal dysplasia. American Journal of Medical Genetics- Part A, 170 (6). pp. 1639-1641. ISSN 1552-4825

Girisha, KM (2016) BGN mutations in X-Linked spondyloepimetaphyseal dysplasia. The American Journal of Human Genetics, 98 (6). pp. 1243-1248. ISSN 0002-9297

Girisha, KM (2016) Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype. Blood, 127 (25). pp. 3154-3164. ISSN 0006-4971

Girisha, KM (2016) Hunting for mutations in Indian patients with hunter syndrome. Indian Pediatrics, 53 (2). p. 117. ISSN 0019-6061

Shetty, Pavanchand and Kumar, Ashwini and Nayak, Vinod C and Patil, Navin and Avinash, A and Shashidhara, Sowmya and Rao, Karthik and Rao, Raghavendra (2016) A rare case of neem oil ingestion as a suicidal modality. Research Journal of Pharmaceutical, Biological and Chemical Sciences, 7 (1). pp. 1253-1255. ISSN 0975-8585

Pais, Maria and Lewis, Leslie and Bhat, Ramesh Y and Jayashree, P (2016) Amniotic Band Sequence with Clubfoot in a Neonate: A Case Report. Manipal Journal of Nursing and Health Sciences, 2 (1). pp. 78-80. ISSN 2395-1397

Shukla, Anju and Upadhyai, Priyanka and Shah, Jhanvi and Neethukrishna, K and Girisha, KM (2016) Autosomal Recessive Spinocerebellar Ataxia 20: Report of a New Patient and Review of Literature. European Journal of Medical Genetics, 60 (2). pp. 118-123. ISSN 1769-7212

Thulasidhar, Adharsh Narain and Kumar, Sandeep and Aroor, Shrikiran and Mundkur, Suneel C (2016) Avascular Necrosis of Femoral Head in a Child with Beta Thalassaemia Major. Journal of Clinical and Diagnostic Research, 10 (9). p. 3. ISSN 0973-709X

Hebbar, Malavika and Shukla, Anju and Girisha, KM (2016) Biallelic Loss of Proprioception-Related PIEZO2 Causes Muscular Atrophy with Perinatal Respiratory Distress, Arthrogryposis, and Scoliosis. The American Journal of Human Genetics, 99. pp. 1206-1210. ISSN 0002-9297

Bhat, Ramesh Y (2016) Bullous Impetigo with Sepsis. European Journal of Pediatric Dermatology, 26 (3). pp. 7-8. ISSN 2281-9649

Hebbar, Malavika and Girisha, KM and Shukla, Anju (2016) Classical cleidocranial dysplasia in an adult, due to a novel frameshift pathogenic variant in RUNX2. BMJ Case Report. pp. 1-3. ISSN 1757-790X

Nayak, Dinesh M and Jha, Ajay and Nayak, Chandrika D (2016) Clinical Profile of Children Presenting with Convulsive Status Epilepticus At a Tertiary Care Hospital in Southern India. International Journal of Pharma and Bio Sciences, 7 (2). pp. 76-80. ISSN 0975-6299

Dogra, Luvdeep and Lewis, Leslie and Bhat, Ramesh Y and Jayashree, P and Najih, M and Shetty, Ranjan and Nayak, Krishnananda (2016) Congenital Absence of Pulmonary Valve: A Rare Congenital Heart Defect in Newborns. International Journal of Cardiovascular Research, 5 (5). pp. 1-3.

Lewis, Leslie and Bhat, Ramesh Y and Jayashree, P and Shetty, Ranjan and Krishnananda, N (2016) Congenital absence of pulmonary valve: A rare congenital heart defect in newborns. International Journal of Cardiovascular Research, 5 (5). pp. 1-3. ISSN 2324-8602

Pawar, Chandrakant and Rao, Pragna and Lewis, Leslie and Moorkoth, Sudheer (2016) Development of a gc-ms Bio-analytical method to detect organic Acidemia in neonatal/ paediatric urine Sample. International Journal Of Pharmacy & Technology, 8 (2). pp. 13110-13124. ISSN 0975-766X

Karun, Kalesh M and Binu, VS and Nair, Sreekumaran N and Prasad, Manjunatha K and Prasad, Keerthana and Girisha, KM (2016) Estimation of correlation between various types of pixel intensities in a single spot. Electronic Journal of Applied Statistical Analysis, 9 (1). pp. 58-69. ISSN 2070-5948

Salian, Smrithi and Vahab, Saadi Abdul and Shukla, Anju and Shah, Hitesh Hasmukhalal and Ramamurhty, B and Shenoy, R and Satyamoorthy, K and Girisha, KM (2016) Evaluation of multiplex ligation dependent probe amplification as a tool for diagnosis and carrier detection in families with a dystrophinopathy. Genetic Counseling, 27 (4). pp. 449-460. ISSN 1015-8146

Salian, Smrithi and Girisha, KM (2016) Focal Dermal Hypoplasia with a De novo Mutation p.E300* of PORCN Gene in a Male Infant. Indian Journal of Dermatology, Venereology, and Leprology, 61 (6). pp. 1-3. ISSN 0378-6323

Uttarillia, A and Girisha, KM (2016) Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type II. Clinical Genetics, 90 (12). pp. 496-508. ISSN 0009-9163

Syed, Farooq and Lewis, Leslie and Bhatt, Ramesh Y and Samanth, Jyothi and Shetty, Kiran (2016) Intracardiac Fungal Ball in A Preterm Newborn with Congenital Heart Disease Complicated by Right Atrial Mycetoma Obstructing Tricuspid Valve. Research Journal of Pharmaceutical, Biological and Chemical Sciences, 7 (5). pp. 2506-2509. ISSN 0975-8585

Ravi, Rohit and Gunjawate, Dhanshree R and Yerraguntla, Krishna and Rajashekhar, B and Lewis, Leslie (2016) Knowledge and Attitude of Parents/caregivers Towards Hearing Loss and Screening in Newborns – A Systematic Review. International Journal of Audiology, 55 (12). pp. 715-722. ISSN 1708-8186

Ravi, Rohit and Yerraguntla, Krishna and Gunjawate, Dhanshree R and Bellur, Rajashekhar and Lewis, Leslie and Guddattu, Vasudeva (2016) Knowledge and attitude (KA) survey regarding infant hearing loss in Karnataka, India. International Journal of Pediatric Otorhinolaryngology, 85. pp. 1-4. ISSN 0165- 5876

Gandham, SriLakshmi Bhavani and Girisha, KM (2016) Metatropic Dysplasia with a Novel Mutation in TRPV4. Indian Pediatrics, 53 (8). pp. 735-737. ISSN 0019-6061

Bhat, Ramesh Y and Lewis, Leslie E and Jayashree, P and Prakashini, K and Shetty, Ranjan K and Nayak, Krishnananda (2016) Neonatal Tuberous Sclerosis Complex with Large and Multiple Cardiac Rhabdomyomas. Iranian Heart Journal, 17 (3). pp. 51-54.

Salian, Smrithi and Gupta, Ashish and Shukla, Anju and Girisha, KM (2016) Novel ALOX12B mutation identified in parents following single nucleotide polymorphism microarray testing of banked DNA from a fatal case of congenital ichthyosis. Indian Journal of Dermatology, 61 (1). pp. 122-125. ISSN 0019-5154

Girisha, KM (2016) PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution. JCI Insight, 1 (9). pp. 1-18. ISSN 2379-3708

Girisha, KM and Bidchol, Abdul Mueed and Gupta, Ashish and Shah, Hitesh (2016) Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients. BMC Medical Genetics, 17 (27). pp. 1-14.

Shukla, Anju and Hebbar, Malavika and Kadavigere, Rajagopal and Girisha, KM (2016) Phenotypic variability in patients with interstitial 6q21-q22 microdeletion and Acro-Cardio-Facial syndrome. American Journal of Medical Genetics- Part A. pp. 1-2. ISSN 1552-4825

Jayashree, Purkayastha and Soundaram, V and Lewis, Leslie and Bhat, Ramesh Y (2016) Postnatal Growth and Short-term Complications in Very Low Birth Weight Neonates Receiving Total Parenteral Nutrition. Indian Journal of Child Health, 3 (1). pp. 1-5. ISSN 2349-6118

Adiga, S and Lewis, Leslie and Tripathy, A (2016) A Prospective Study of Antimicrobial Utilisation and Cost Pattern Analysis in the Treatment of Neonatal Sepsis in a Tertiary Care Hospital. nternational Journal of Current Pharmaceutical Review and Research, 7 (5). pp. 291-295. ISSN 0976 822X

Nayak, Dinesh M (2016) A Randomized Trial of Factor VIII and Neutralizing Antibodies in Hemophilia A. New England Journal of Medicine, 374 (21). pp. 2054-2064. ISSN 0028-4793

Rao, Raghavendra and Girisha, KM (2016) Unusual Skin Manifestations in a Patient with Menkes Disease. American Journal of Medical Genetics- Part A, 170 (11). pp. 3039-3040. ISSN 1552-4825

Shetty, Shricharith and Bhaskaranand, Nalini (2016) Yellow Nail Syndrome. Indian Pediatrics, 53 (12). p. 1133.

Girisha, KM and Shukla, Anju and Bhavani, Gandham SriLakshmi and Hebbar, Malavika and Rajagopal, KV (2016) A homozygous nonsense variant in IFT52 is associated with a human skeletal ciliopathy. Clinical Genetics, 90 (12). pp. 536-539. ISSN 0009-9163

Sharma, Swati and Gupta, Ashish and Jaiprakash, Padmapriya (2015) Solitary eruptive vellus hair cyst in an adult- An unusual presentation: Case report with a brief review of literature. International Journal of Health Sciences and Research, 5 (6). pp. 733-736. ISSN 2249-9571

Bhavani, Gandham SriLakshmi and Girisha, KM (2015) Novel mutation in an Indian patient with transcobalamin II deficiency. The Indian Journal of Pediatrics. pp. 1-2. ISSN 0019-5456

Mundkur, Suneel C and Kumar, Sandeep and Hebbar, Shrikiran (2015) Common variable immunodeficiency associated with partial albinism. Pediatric Oncall Journal, 12 (2). pp. 1-3. ISSN 0973-0958

Karun, Kalesh M and Binu, VS and Prasad, Keerthana and Nair, Sreekumaran N and Prasad, Manjunath K and Girisha, KM (2015) Review on image segmentation methods in cDNA microarray experiments and a novel algorithm for segmentation. International Journal of Emerging Science and Engineering (IJESE), 3 (5). pp. 23-24. ISSN 2319–6378

Bidchol, Abdul Mueed and Girisha, KM (2015) White matter changes in GM1 gangliosidosis. Indain Pediatrics, 52. pp. 155-156.

Patra, Saikat and Bhat, Ramesh Y and Lewis, Leslie and Purakayastha, Jayasheree and Vamsi, Sivarama Raju (2015) Cerebral abscess due to serratia marcescens\. Indian Journal of Pediatrics, 82 (2). pp. 199-200. ISSN 0019-5456

Kumar, Maneesh and Hebbar, Shrikiran and Mundkur, Suneel C and Kumar, Sandeep (2015) Guillain-Barré syndrome: A clinical study of twenty children. Journal of Clinical and Diagnostic Research, 9 (1). SC09-SC12. ISSN 0973-709X

Nayak, Shalini S and Shukla, Anju and Lewis, Leslie and Kadavigere, Rajagopal and Mathew, Mary and Adiga, Prashanth K and Vasudeva, Akhila and Kumar, Pratap and Shetty, Jyothi and Shah, Hitesh and Girisha, KM (2015) Clinical Utility of Fetal Autopsy and Its Impact on Genetic Counseling. Prenatal Diagnosis, 35. pp. 1-7.

Shukla, Anju and Girisha, KM (2015) Co-Occurrence of a De Novo Williams and 22q11.2 microdeletion syndromes. American Journal of Medical Genetics Part A, 167 (4). pp. 1-5.

Khurana, S and Rao, Bhamini K and Lewis, Leslie and Kumaran, Senthil D and Kamath, Asha (2015) Effect of structured neonatal physiotherapy intervention on neurobehavior of moderate to late preterm infants—a randomized controlled trial. Physiotherapy, 101 (Sup-1). eS745-eS745.

Salian, Smrithi and Girisha, KM (2015) Familial 7q11.23 Duplication With Variable Phenotype. American Journal of Medical Genetics. pp. 1-4.

Purkayastha, Jayashree and Lewis, Leslie and Bhat, Ramesh Y and Anusha, KM (2015) Feasibility and Safety of Therapeutic Hypothermia and Short Term Outcome in Neonates with Hypoxic Ischemic Encephalopathy. Indian Journal of Pediatrics. pp. 1-3.

Madireddi, Jagadesh and Sarada, P and Shetty, RK and Prabhu, Mukhyaprana and Girisha, KM (2015) Hunter syndrome with its typical heart: a close mimic to rheumatic heart. BMJ Case Report. pp. 1-5. ISSN 1757-790X

Gupta, Ashish and Uttarilli, Anusha and Dalal, Ashwin B and Girisha, KM (2015) Hunter syndrome with late age of presentation: clinical description of a case and review of the literature. BMJ Case Report. pp. 1-3. ISSN 1757-790X

Nalini, K and Shenoy, Vijetha Belle and Kini, Pushpa G and Jacob, Prince and Rao, Pragna (2015) Novel Urinary and Plasma Biochemical Findings in a Child with Recurrent Respiratory Infections. Asia Pacific Journal of Research, 1 (14). pp. 26-30. ISSN 2347-4793

Bhavani, Gandham SriLakshmi and Shah, Hitesh and Shukla, Anju and Girisha, KM (2015) Novel and recurrent mutations in WISP3 and an atypical phenotype. American Journal of Medical Genetics Part A. pp. 1-4.

Meenu, J and Mundkur, Suneel C and Aroor, Shraikiran and Nalini, B and Kini, Pushpa (2015) Outcome of Organophosphate Poisoning in Children in a Ttertiary Care Hospital. Journal of Disease and Global Health, 3 (3). pp. 94-97. ISSN 2454-1842

Bidchol, Abdul Mueed and Shukla, Anju and Hebbar, Shrikiran and Bhat, Ramesh Y and Matta, Divya and Shah, Hitesh and Gopinath, PM and Satyamoorthy, K and Girisha, KM (2015) Recurrent and novel GLB1 mutations in India. Gene, 40 (485). pp. 1-9. ISSN 0378-1119

Bellampalli, Ravishankara and Phani, Nagaraja M and Bhaskaranand, Nalini and Kanive, Guruprasad P and Rai, Padmalatha S and Satyamoorthy, K (2015) Significance of 5,10-methylenetetrahydrofolate Reductase gene Variants in acute Lymphoblastic Leukemia in Indian Population: An Experimental, Computational and Meta-analysis. Leukemia & Lymphoma, 56 (5). pp. 1450-1459. ISSN 1029-2403

Nayak, Shalini S and Shukla, Anju and Kodandapani, Sreelakshmi and Adiga, Prashanth K and Girisha, KM (2015) What does fetal autopsy unmask in oligohydramnios? The Journal of Maternal-Fetal & Neonatal Medicine. pp. 1-5. ISSN 1476-7058

Hebbar, Shrikiran and Kumar, Sandeep and Mundkur, Suneel C and Kumar, Maneesh (2014) Hemolytic uremic syndrome associated with dengue fever in an adolescent girl. Indian Journal of Pediatrics, 81 (12). pp. 1397-1398. ISSN 0019-5456

Patra, Saikat and Bhat, Ramesh Y and Lewis, Leslie and Purakayastha, Jayashree and Vamsi, Sivarama Raju and Kalwaje, Vandana E and Mishra, Swathi (2014) Burkholderia cepacia sepsis among neonates. Indian Journal of Pediatrics, 81 (11). pp. 1233-1236. ISSN 0019-5456

Kumar, Sandeep (2014) Role of oral midazolam as a procedural sedative in children aged 6 months to 12 years. International Journal of Pharma and Bio Sciences, 5 (4). pp. 488-495. ISSN 0975-6299

Sravanthi, K and Mundkur, Suneel C and Hebbar, Shrikiran and Kumar, Sandeep and Kashyap, Harish (2014) Yellow oleander poisoning in children- A report of two cases. Pediatric Oncall, 11 (4). pp. 117-118.

Margaret, Binu E and Shetty, Sheela and Lewis, Leslie and Bhat, Ramesh Y (2014) Maternal anxiety and family support among mothers of neonates admitted in Neonatal Intensive Care Unit. IOSR Journal of Nursing and Health Science (IOSR-JNHS), 3 (5). pp. 40-43. ISSN 2320–1940

Girisha, KM (2014) Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism. Journal of Medical Genetics. pp. 1-10.

Mundkur, Suneel C and Kumar, Sandeep and Hebbar, Shrikiran (2014) Fatal viral pneumonia associated with rhinovirus in a healthy infant. Karnataka Paediatric Journal, 29 (3). pp. 125-127.

D'Souza, Sonia RB and Kumar, Vijay and Lewis, Leslie (2014) Development of a tool for assessing preterm infants. Nursing and Midwifery Research Journal, 10 (3). pp. 91-99.

Kumar, Praful AK and Margaret, Binu and Jyothi, RK and Lewis, Leslie and Hariprakash, * (2014) Effectiveness of sensitization program on knowledge of staff regarding noise in neonatal intensive care unit of Kasturba Hospital, Manipal. International Journal of Nursing Education, 6 (2). pp. 20-23. ISSN 0974-9349

Mundkur, Suneel C and Kumar, Sandeep and Hebbar, Shrikiran and Kumar, Maneesh (2014) Iatrogenic Cushing`s syndrome in a child following topical ocular steroid therapy. Pediatric Oncall Journal, 12 (3). p. 90.

Prabhu, Krishnananda and Malik, Rimshida and Pai, Priya and Gayathri, S and Rao, Anjali and Bhaskaranand, Nalini (2014) Role of renoprotective therapy on antioxidant status in children with nephrotic syndrome. Journal of international academic research for multidisciplinary, 2 (4). pp. 576-581. ISSN 2320-5083

Girisha, KM (2014) The SMAD-binding domain of SKI: a hotspot for de novo mutations causing Shprintzen–Goldberg syndrome. European Journal of Human Genetics. pp. 1-5.

Girisha, KM (2014) CFTR Mutations in India: Need to do More! Gemetocost's perspective. Indian Pediatrics, 51. pp. 177-178.

Kumar, Sandeep and Hebbar, Shrikiran and Mundkur, Suneel C and Kumar, Maneesh (2014) Infective tropical acute kidney injury in an adolescent from rural coastal Karnataka - A case report. Karnataka Paediatric Journal, 29 (1). pp. 11-13.

Vamsi, Sivarama Raju and Bhat, Ramesh Y and Lewis, Leslie E and Kalwaje, Vandana E (2014) Time to Positivity of Blood Cultures in Neonates. Pediatric Infectious Disease Journal, 33 (2). pp. 212-214.

Girisha, KM and Bhavani, Gandham SriLakshmi and Shah, Hitesh (2014) A Syndrome of Facial Dysmorphism, Cubital Pterygium, Short Distal Phalanges, Swan Neck Deformity of Fingers, and Scoliosis. American Journal Of Medical Genetics Part - A. pp. 1-6.

Manjula, * and Ansuya, * and Kamath, Asha and Mundkur, Suneel C (2014) An evaluative study to find the effectiveness of two methods of management of pediculosis capitis among children of selected schools of Udupi District. IOSR Journal of Nursing and Health Science (IOSR-JNHS), 3 (1). pp. 17-20. ISSN 2320-1940

Rao, Krishna A and Jayashree, Purkayastha and Hazarika, Manali and Raghuvamsi, Chaitra and Mithun, Adith KS (2014) Analysis of prenatal and postnatal risk factors of retinopathy of prematurity in tertiary care hospital in South India. Indian Journal of Ophthalmology, 62 (9). pp. 972-973.

Bhandarkar, Ajay M and Nayak, Ramya and Chidambaranathan, Nithyanand and Gopinath, Divya (2014) Beware of a pulsating oropharynx. BMJ Case Reports. pp. 1-2.

Mathew, Mary and Jaiprakash, Padmapriya and Rao, Lakshmi and Bhaskaranand, Nalini (2014) A Case of Congenital Embryonal Rhabdomyosarcoma, Presenting as Blueberry Muffin Baby. Iranian Journal of Pathology, 9 (2). pp. 156-159.

Datta, Priyanka and Prasad, Anushre and Shenoy, Vijetha Belle and Hebbar, Shrikiran A and Mundkur, Suneel C and Rao, Pragna (2014) A Case of Sanfillippo’s Disease Correlating Clinical and Biochemical Findings. Indian Journal of Clinical Biochemistry. pp. 3-6. ISSN 0970-1915

Subramaniam, Nathiya and Mundkur, Suneel C and Kini, Pushpa and Bhaskaranand, Nalini and Hebbar, Shrikiran (2014) Clinicohematological study of thrombocytosis in children. ISRN Hematology, 2014. pp. 1-4.

Bhat, Ramesh Y and Varma, Chaitanya PV and Bhatt, Sonia (2014) Dengue fever with co-infections: A case series in children. Journal of Microbiology and Infectious Diseases (1). S62-S64. ISSN 2146-3158

Girisha, KM (2014) Eight Years Experience from a Skeletal Dysplasia Referral Center in a Tertiary Hospital in Southern India: A Model for the Diagnosis and Treatment of Rare Diseases in a Developing Country. American Journal Of Medical Genetics - Part - A, 9999. pp. 1-7.

Girisha, KM (2014) Exome Sequencing Identifies a Dominant TNNT3 Mutation in a Large Family with Distal Arthrogryposis. Molecular Syndromology. pp. 1-11.

Nayak, Shalini S and Kadavigere, Rajagopal and Mathew, Mary and Kumar, Pratap and Girisha, KM (2014) Fetal Akinesia Deformation Sequence: Expanding the Phenotypic Spectrum. American Journal of Medical Genetics. pp. 1-6.

Bhat, Ramesh Y and Ramdas, Vidya (2014) Frequency and Intensive Care Related Risk Factors of Pneumothorax in Ventilated Neonates. Pulmonary Medicine (2014). pp. 1-5.

Bidchol, Abdul Mueed and Shah, Hitesh and Satyamoorthy, K and Girisha, KM (2014) GALNS Mutations in Indian Patients With Mucopolysaccharidosis IVA. American Journal of Medical Genetics Part - A, 9999. pp. 1-9.

Mohan, Swathy and Skariah, Tisha Ann and Eribaweimon, Shilla and Lewis, Leslie (2014) Graded oxygen delivery using low flow rotameter during positive pressure ventilation using self-inflating bag with a leak - an experimental study. Indian Journal of Respiratory Care, 3 (1).

Bhat, Ramesh Y and Kakkar, Shruti and Prakashini, K (2014) Hemiconvulsion-hemiplegia-Epilepsy syndrome: Clinical course and Neuroradiological Features in a 20-month-old Girl. BMJ Case Report. pp. 1-3.

Bhat, Ramesh Y and Patra, Saikat and Varma, Chaitanya PV and Prakashini, K (2014) Hypomelanosis of Ito with an Unusual Pulmonary Abnormality in an Infant. Indian Dermatology Online Journal , 5 (2). pp. 196-197.

Bhat, Ramesh Y and Varma, Chaitanya PV and Bhatt, Sonia (2014) An Infant with Chronic Severe Neutropenia. BMJ Case Report. pp. 1-3.

Shah, Krupa H and Sarpangala, Shailaja and Girisha, KM (2014) Is Coloboma a Feature of Fetal Valproate Syndrome? Clinical Dysmorphology, 23. pp. 24-25.

Kumar, Sandeep and Hebbar, Shrikiran and Mundkur, Suneel C and Kumar, Maneesh (2014) Merosin-deficient congenital muscular dystrophy with cerebral white matter changes: a clue to its diagnosis beyond infancy. BMJ Case Report. pp. 1-3. ISSN 1757-790X

Girisha, KM (2014) Microduplications Encompassing the Sonic Hedgehog Limb Enhancer ZRS are Associated with Haas Type Polysyndactyly and Laurin-Sandrow Syndrome. Clinical Genetics. pp. 1-18.

Girisha, KM and Shah, Hitesh (2014) Mutation Spectrum of COL1A1 and COL1A2 Genes in Indian Patients With Osteogenesis Imperfecta. American Journal Of Medical Genetics Part -A, 9999. pp. 1-8.

Girisha, KM and Shah, Hitesh (2014) Mutations in patients with osteogenesis imperfecta from consanguineous Indian families. European Journal of Medical Genetics. pp. 1-7. ISSN 1769-7212

Girisha, KM and Bidchol, Abdul Mueed and Kamath, Preeti S and Shah, Krupa H and Shah, Hitesh (2014) A Novel Mutation (g.106737G>T) in Zone of Polarizing Activity Regulatory Sequence (ZRS) Causes Variable Limb Phenotypes in Werner Mesomelia. American Journal Of Medical Genetics Part-A, 9999. pp. 1-9.

Girisha, KM (2014) Organization for rare diseases India (ORDI) – addressing the challenges and opportunities for the Indian rare diseases’ community. Genetics Research Cambridge, 96 (9). pp. 1-10.

Soundaram, V and Bhat, Ramesh Y and Lewis, Leslie and Girisha, KM and Jayashree, P and Balasubramanian, Sudha and Pratyusha, R (2014) Pfeiffer syndrome with extreme proptosis, hypothyroidism and tail like appendage. Oman Medical Journal, 29 (5). pp. 1-3.

Kamath, Saritha U and Bhaskaranand, Nalini and Rao, Anjali (2014) Role of early intervention in a family of affected siblings with suspected mitochondrial disorder. World Journal of Pharmaceutical Researech, 3 (2). pp. 2226-2231. ISSN 2277 – 7105

Bhat, Ramesh Y and Varma, Chaitanya PV and Bhatt, Sonia and Balachandran, C (2014) Rowell syndrome. Indian Dermatology Online Journal, 5 (S-1). S33-S35. ISSN 2229-5178

Rajeshwari, SG and Choudhry, Afreen Arshad and Prasad, Anushre and Lewis, Leslie and Shenoy, Revathi P and Rao, Pragna (2014) Short Chain Acyl Co-A Dehydrogenase Deficiency A Rare Inborn Error Of Metabolism. National Journal of Integrated Research in Medicine, 5 (1). pp. 125-127. ISSN 0975 - 9840

Bhat, Ramesh Y and Kumar, Pavan CG (2014) Sixth hour Transcutaneous Bilirubin Predicting Significant Hyperbilirubinemia in ABO Incompatible Neonates. World Journal of Pediatrics , 10 (2). pp. 182-185.

Kamath, Saritha U and Bhaskaranand, Nalini and Rao, Anjali (2014) Spectrum of Clinical Symptoms in Children with Elevated Lactate: Pyruvate Ratio in a Tertiary Care Setting. Asian Journal of Biomedical and Pharmaceutical Sciences, 4 (29). pp. 34-38. ISSN 2249-622X

Nayak, Shalini S and Adiga, Prashanth K and Girisha, KM (2014) Symmetrical Terminal Transverse Limb Deficiencies. Indian Journal of Pediatrics. pp. 1-2.

Hebbar, Shrikiran and Kumar, Sandeep and Mundkur, Suneel C (2014) Transient cutaneous hyperpigmentation of extremities following dengue fever. Our Dermatolology Online, 5 (3). pp. 298-299.

Bhat, Ramesh Y and Kurien, Annamma and Kakkar, Shruti and Padma, MS and Raju, Vamsi Sivarama and George, Sherin (2013) Spontaneous recovery of haemophagocytic syndrome in an adolescent girl receiving anti-tuberculosis treatment. Journal of Microbiology and Infectious Diseases, 3 (4). pp. 211-213.

Rao, Krishna A and Purkayastha, Jayashree and Hazarika, Manali and Raghuvamsi, Chaitra and Adith, Mithun K (2013) Analysis of prenatal and postnatal risk factors of retinopathy of prematurity in a tertiary care hospital in South India. Indian Journal of Ophthalmology, 61 (11). pp. 640-644.

Girisha, KM and Bidchol, Abdul Mueed and Sarpangala, Murali Keshava and Satyamoorthy, K (2013) A Novel Frameshift Mutation in TWIST2 Gene Causing Setleis Syndrome. The Indian Journal of Pediatrics. pp. 1-3. ISSN 0019-5456

Bhat, Ramesh Y and Shah, Vishal Kumar Bharath (2013) Prevalence of malnutrition among under-five year old children with acute lower respiratory tract infection hospitalized at Udupi District Hospital. Archives of Pediatric Infectious Diseases, 1 (5). pp. 203-206.

Shastry, Shamee and Lewis, Leslie and Bhat, Sudha S (2013) A rare case of haemolytic disease of newborn with Bombay phenotype mother. Asian Journal of Transfusion Science, 7 (2). pp. 153-155. ISSN 0973-6247

Ballal, Mamatha and Chakraborty, Rituparna and Mundkur, Suneel C and Aroor, Shrikiran and Balakrishnan, Abirhami and Rajalingam, Vijianthy (2013) An Unusual Presentation of Acute Gastroenteritis Caused by Elizabethkingia Meningoseptica in a Child with Sepsis from Rural Karnataka-A Case Report. Journal of International Medical Sciences Academy (JIMSA), 26 (2). pp. 114-115. ISSN 0971 - 071X

Varma, Chaitanya PV and Bhatt, Sonia and Bhat, Ramesh Y (2013) Amitraz Poisoning. Indian Journal of Pediatrics, 80 (4). pp. 349-350. ISSN 0019-5456

John, Neetha and Rajasekhar, Moka and Girisha, KM and Sharma, Podila Satya Venkata Narasimha and Puthiya, Gopinath Mundyat (2013) Multiplex ligation-dependant probe amplification study of children with idiopathic mental retardation in South India. Indian Journal of Human Genetics, 19 (2). pp. 163-168.

Bhat, RY and Manjunath, N (2013) Correlates of acute lower respiratory tract infections in children under 5 years of age in India. The International Journal of Tuberculosis and Lung Disease, 17 (3). pp. 418-422.

Bhat, Ramesh Y and Varma, Chaitanya (2013) Meningitis as a primary presentation of Dengue infection. Journal of Microbiology and Infectious Diseases, 3 (1). pp. 39-40. ISSN 2146-3158

Nayak, S and Rawal, Asha and Adiga, Prashanth K and Rai, Lavanya and Girisha, KM (2013) Single forearm bone on antenatal scan: Diagnosis of VACTERL association on autopsy. Genetic Clinics, 6 (1). pp. 1-18.

Maddukuri, Satish Babu and Girisha, KM (2013) Expanding the Phenotype Associated With 17q12 Duplication: Case Report and Review of the Literature. American Journal of Medical genetics Part A, 161 (2). pp. 352-359.

Rao, Bhamini K and Kamath, Asha and Lewis, Leslie and Mohan, Divya (2013) Effect of Stimulation on Neuromotor Development in Preterm Infants. The Indian Journal of Pediatrics. ISSN 0019-5456

Skariah, Tisha Ann and Lewis, Leslie and Sasi, Arun (2013) Noninvasive ventilation in preterm neonates - Nasal continuous positive airway pressure vS Nasal intermittent positive pressure ventilation – A randomised controlled trial. Indian Journal of Respiratory Care, 2 (1). pp. 206-212.

Varma, Chaitanya PV and Bhat, Ramesh Y and Bhatt, Sonia (2013) Bardet-Biedl syndrome in two sisters: A rare incidence. Journal of Pediatric Genetics, 2 (1). pp. 49-52. ISSN 2146-4596

Bhat, Ramesh Y and Shah, Vishal Kumar Bharath and Elangovan, Deepak (2013) Clinical characteristics and fever resolution time in 113 children with malaria from a centre in Karnataka, India. Journal Journal of Pediatric Infectious Diseases, 8 (3). pp. 111-115. ISSN 1305-7707

Nayak, Chandrika D and Agarwal, Vaibhav and Nayak, Dinesh M (2013) Correlation of Cord Blood Lipid Heterogeneity in Neonates with Their Anthropometry at Birth. Indian Journal of Clinical Biochemistry, 28 (2). pp. 152-157.

Bhat, Ramesh Y and Kakkar, S and Balachandran, C and Rao, Lakshmi and Roopasree, S (2013) Erythrodermic psoriasis. European Journal of Pediatric Dermatology, 23. pp. 142-144.

Phani, Nagaraja M and Acharya, Shreeshakala and Xavy, Seethu and Bhaskaranand, Nalini and Bhat, Manoj K and Jain, Aditya and Rai, Padmalatha S and Satyamoorthy, K (2013) Genetic Association of KCNJ10 rs1130183 with Seizure Susceptibility and Computational Analysis of Deleterious non-synonymous SNPs of KCNJ10 Gene. Gene, 536 (2). pp. 247-253.

Girisha, KM (2013) Genotype–phenotype spectrum of PYCR1-related autosomal recessive cutis laxa. Molecular Genetics and Metabolism, xxx. pp. 1-10.

Nayak, Deepak M and Manohar, Chethan and Nalini, B (2013) Hemophagocytic lymphohistiocytosis masquerading as sepsis. International Journal of Clinical and Surgical Advances , 1 (1). pp. 2-5. ISSN 2321-9351

Girisha, KM and Nayak, Shalini S and Rawal, Asha and Roopa, Padavagodu S and Shetty, Jyothi (2013) Jejunal atresia and postaxial polydactyly: a newly recognized phenotype. Clinical Dysmorphology, 22 (3). pp. 121-123.

David, Lydia and D'Souza, Sonia RB and Prabhu, Anasuya and Lewis, Leslie (2013) Learning Needs and Nursing care Needs of Postnatal Women: Perception of Women and the Nurses. i-manager’s Journal on Nursing, 2 (4). pp. 20-24. ISSN 2231-4504

Bhat, Ramesh Y (2013) Neonatal thrombocytopenia and pregnancy induced hypertension. Salud(i) Ciencia, 20. pp. 270-273.

Girisha, KM (2013) Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders. European Journal of Human Genetics, 21. pp. 1074-1078.

Bhat, Ramesh Y and Ramdas, V (2013) Predisposing Factors, Incidence and Mortality of Pneumothorax in Neonates. Minerva Pediatrica , 65 (4). pp. 383-388.

Vivek, G and Shetty, Ranjan K and Nayak, Shalini S and Girisha, KM and Naha, Kushal (2013) Prenatal diagnosis of absent pulmonary valve confirmed by autopsy. BMJ Case Report. pp. 1-3.

Bhat, Ramesh Y and Varma, Chaitanya PV (2013) Reversible hypopigmentation of hair secondary to Vitamin B12 deficiency. Our Dermatol Online, 4 (1). pp. 101-102.

Hebbar, Shrikiran and Varma, Chaitanya PV and Mundkur, Suneel C (2012) Purpura fulminans in a child: A case report. Journal of Clinical and Diagnostic Research, 6 (10). pp. 1812-1813. ISSN 0973-709X

Hebbar, Shrikiran and Varma, Chaitanya PV and Mundkur, Suneel C (2012) Blue rubber-Bleb nevus syndrome which was associated with an atrial septal defect: A case report. Journal of Clinical and Diagnostic Research, 6 (9). pp. 1566-1567. ISSN 0973-709X

Nayak, Dinesh M and Nayak, Chandrika D (2012) Implementing office paediatrics in undergraduate medical curriculum: An ideal opportunity for learning paediatric practices in a realistic picture. International Journal of A J Institute of Medical Sciences, 1 (2). pp. 152-155.

Varma, Chaitanya PV and Hebbar, Shrikiran and Mundkur, Suneel C and Annamalai, Karthick (2012) Bilateral type-I duane syndrome with multiple anamolies: A case report. Journal of Clinical and Diagnostic Research, 6 (8). pp. 1435-1436. ISSN 0973-709X

Nayak, Chandrika D and Kamath, Madhava and Nayak, Dinesh M and Nagesha, KM (2012) Status of Pituitary-Thyroid Axis of Newborns and its Relationship with Anthropometry and Maternal Factors at Birth. International Journal of Pharma and Bio Sciences, 3 (4). pp. 51-57.

Shah, Hitesh and Girisha, KM (2012) Growth Retardation, Intellectual Disability, Facial Anomalies, Cataract, Thoracic Hypoplasia, and Skeletal Abnormalities: A Novel Phenotype. American Journal of Medical Genetics Part - A. pp. 1-5.

Varma, Chaitanya PV and Bhat, Ramesh Y and Bhatt, Sonia (2012) Unilateral open‑lip schizencephaly: A rare cause of infantile hemiparesis. Journal of Pediatric Neurosciences, 7 (3). pp. 234-235. ISSN 1817-1745

Eribaweimon, Shilla and Kini, Pushpa (2012) Paediatric mechanical ventilation. Indian Journal of Respiratory Care, 1 (2). pp. 124-134.

Ratti, Sneha and Lewis, Leslie and Purkayastha, Jayashree and Bhat, Ramesh (2012) An addition of tidal volume (volume guarantee) to synchronised intermittent mandatory ventilation in neonates with respiratory distress syndrome – A randomised controlled trial. Indian Journal of Respiratory Care, 1 (2). pp. 135-139.

Girisha, KM and Pratap, Deepika and Shah, Hitesh (2012) Further characterization of acro-renal-uterine-mandibular syndrome: report of a case and review of earlier reports. Clinical Dysmorphology, 21 (2). pp. 83-86. ISSN 0962-8827

Bhat, Ramesh Y and Kumar, Naveen (2012) Isolated Bilateral Severe Fetal Hydrothorax: Complete Resolution following a Single Postnatal Thoracocentesis. Indian Journal of Pediatrics, 79 (3). pp. 392-394.

Pais, Maria and Devi, Elsa Sanatombi and Pai, Muralidhar V and Lewis, Leslie and Geroge, Anice and Mayya, Shreemathi S and Bairy, KL (2012) Neonatal sepsis, bacterial isolates and antibiotic susceptibility patterns among neonates. The Nursing Journal of India, 103 (1). pp. 18-20.

Varma, Chaitanya PV and Hebbar, Shrikiran A and Bhat, Ramesh Y and Mundkur, Suneel C and Annamalai, Karthick and Bhatt, Sonia (2012) Antigolgi antibodies in a case of autoimmune haemolytic anemia: a case report. Asian Pacific Journal of Tropical Biomedicine, 2 (1). S462-S463.

Eribaweimon, Shilla and Lewis, Leslie (2012) Basic neonatal and paediatric mechanical ventilation. Indian Journal of Respiratory Care, 1 (1). pp. 21-27.

Annamalai, Karthick and Hebbar, Shrikiran and Mundkur, Suneel C and Varma, Chaitanya PV (2012) EEC syndrome with renal anomalies . a rare association. Karnataka Paediatric Journal, 26 (1). pp. 6-7.

Varma, Chaitanya PV and Hebbar, Shrikiran and Mundkur, Suneel C (2012) Necrotising enterocolitis in a forty day old infant: a case report. Karnataka Paediatric Journal, 26 (1). pp. 32-33.

Eribaweimon, Shilla and Lewis, Leslie (2012) Noninvasive respiratory support in the preterm neonate with hyaline membrane disease: Bubble CPAP vs Conventional CPAP - A randomised controlled trial. Indian Journal of Respiratory Care, 1 (1). pp. 42-46.

Mukhopadhyay, C and Vandana, KE and Munim, F and Lewis, Leslie (2012) Suppurative sialadenitis in a neonate by methicillin-resistant Staphylococcus aureus: Do we need search and kill superbug strategy? Indian Journal of Medical Microbiology, 30 (1). p. 113.

Annamalai, Karthick C and Hebbar, Shrikiran and Mundkur, Suneel C and Varma, Chaitanya PV (2012) Acute naphthalene toxicity presenting with metabolic acidosis: a rare complication. Journal of Acute Disease, 1 (1). pp. 75-76.

Shah, Hitesh and Vijayan, Sandeep and Girisha, KM (2012) Analysis of the WISP3 Gene in Indian Families With Progressive Pseudorheumatoid Dysplasia. American Journal of Medical Genetics Part - A. pp. 1-9.

Bhat, Ramesh Y and Vinayaka, G and Kodandapani, Sreelakshmi (2012) Antenatal Bartter Syndrome: A Review. International Journal of Pediatrics. pp. 1-5.

Bhat, Ramesh Y and Manjunath, N and Sanjay, D and Dhanya, Y (2012) Association of indoor air pollution with acute lower respiratory tract infections in children under 5 years of age. Paediatrics and International Child Health, 32 (3). pp. 132-135.

Eribaweimon, Shilla and Lewis, Leslie (2012) Basic neonatal and paediatric mechanical ventilation. Indian Journal of Respiratory Care, 1 (1).

Gupta, Yogesh Kumar and Prasad, Anushre and Kini, Pushpa and Naik, Prashant and Choprra, Deepti and Prabhu, Krishnananda (2012) Case Report on an Infant Presenting with Hypoglycemia, and Milky Serum. Asian Pacific Journal of Tropical Biomedicine, 2 (4). pp. 331-332.

Naik, Prashant and Kini, Pushpa and Chopra, Deepti and Gupta, Yogesh Kumar (2012) Finlay-Marks syndrome: Report of two siblings and review of literature. American Journal of Medical Genetics - Part - A, 158A. pp. 1696-1701.

Varma, Chaitanya PV and Hebbar, Shrikiran and Mundkur, Suneel C and Karthick, A (2012) Gifted children in pediatric practice. WebmedCentral, 3 (1). pp. 1-4. ISSN 2046-1690

Varma, Chaitanya PV and Hebbar, Shrikiran and Mundkur, Suneel C and Annamalai, Karthick (2012) Kawasaki disease with peripheral gangrene and autoamputation - an extremely rare complication: A case report. Our Dermatology Online, 3. pp. 210-211. ISSN 2081-9390

Tercier, Stephane and Siddesh, ND and Shah, Hitesh and Girisha, KM and Joseph, Benjamin (2012) Loss of a condyle of the femur or tibia following septic arthritis in infancy: problems of management and testing of a hypothesis of pathogenesis. Journal of Children Orthopaedics.

Chaudhary, Narendra and Borker, Anupama (2012) Metronomic Therapy for Malignant Peripheral Nerve Sheath Tumor in Neurofibromatosis Type 1. Pediatric Blood & Cancer. pp. 1-3.

Bhat, YR and Kumar, Pavan CG (2012) Morbidity of ABO haemolytic disease in the newborn. Paediatrics and International Child Health, 32 (2). pp. 93-96.

Girisha, KM and Satyamoorthy, K (2012) Mucolipidosis Type II a/b With a Homozygous Missense Mutation in the GNPTAB Gene. American Jornal of Medical Genetics Part-A, 158-A. pp. 1225-1228.

Eribaweimon, Shilla and Lewis, Leslie (2012) Noninvasive respiratory support in the preterm neonate with hyaline membrane disease: Bubble CPAP vs Conventional CPAP - A randomised controlled trial. Indian Journal of Respiratory Care, 1 (1).

Girisha, KM and Aroor, Shrikiran and Bidchol, Abdul Mueed and Puthiya, Gopinath Mundyat and Satyamoorthy, K (2012) Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type. Indian Journal of Human Genetics, 18 (3). pp. 346-348.

Adiga, Prashanth and Rai, Lavanya and Girisha, KM and Mundkur, Anjali (2012) Placental Teratoma Presenting as a LobulatedMass behind the Neck of Fetus: A CaseReport. Case Reports in Obstetrics and Gynecology, 2012. pp. 1-2.

Nayak, SS and Adiga, PK and Rai, Lavanya and Girisha, KM (2012) Severe Rhizomelic Chondrodysplasia Punctata in a Fetus due to Maternal Mixed Connective Tissue Disorder. Genetic Counseling, 23 (4). pp. 487-491.

Chaudhary, Narendra and Kosaraju, Kranthi and Bhat, Kamalakshi and Bairy, Indira and Borker, Anupama (2012) Significance of Interleukin-6 (IL-6) and C-reactive Protein (CRP) in Children and Young Adults With Febrile Neutropenia During Chemotherapy for Cancer: A Prospective Study. Journal of Pediatric Hematology and Oncology.

Varma, Chaitanya PV and Hebbar, Shrikiran and Mundkur, Suneel C and Annamalai, Karthick C (2012) Skin branding in Indian children: A still prevaling superstition in the Modern Era. WebmedCentral PAEDIATRICS, 3 (1). pp. 1-4. ISSN 2046-1690

Roach, Erna Judith and Bhaskaranand, Nalini (2012) A Study on the Effectiveness of an Educational Package on the Knowledge of Mothers of Asthmatic Children on Bronchial Asthma. Journal of Biology,Agriculture and Healthcare, 2 (10). pp. 24-31. ISSN 2224-3208

Pandey, Deeksha and Mishra, Supriya Sundar and Raheja, Rahul and Abha, Shrestha and Saxena, Aashish and Lewis, Leslie (2012) Surfactant Era and Obstetric Decision Making. Sri Lanka Journal of Obstetrics and Gynaecology, 34 (3). pp. 99-105.

Kodandapani, Sreelakshmi and Shetty, Jyothi and Kumar, Pratap and Girisha, KM (2012) Umbilical cyst due to patent urachus in a fetus with complete urorectal septum malformation sequence. Journal of Pediatric Genetics, 1 (1). pp. 59-61.

Varma, Chaitanya PV and Hebbar, Shrikiran and Mundkur, Suneel C and Karthick, A (2012) Virtual reality as a tool in pediatric rehabilitation. WebmedCentral PAEDIATRICS, 3 (1). pp. 1-4. ISSN 2046-1690

Varma, Chaitanya PV and Hebbar, Shrikiran and Mundkur, Suneel C (2012) An atypical giant mantoux reaction. Our Dermatology Online, 3 (3). p. 234.

Neetha, J and Girisha, KM and Gopinath, PM and Sekhar, MR (2012) A de Novo Translocation of Chromosomes 1 and 2 in an 18 Year old boy with Syndromic Mental Retardation. GENETIC COUNSELING, 23 (4). pp. 473-476.

Mundkur, Suneel C and Aroor, Shrikiran and Jayashree, K (2011) Disseminated strongyloidiasis in a immunocompromised host. Indian Pediatrics, 48. pp. 974-976.

Chaudhary, Narendra and Majeed, Rubeena and Borker, Anupama (2011) Isolated cerebellar involvement in posterior reversible encephalopathy syndrome in a child with acute lymphoblastic leukemia. Indian Journal of Medical and Paediatric Oncology, 32 (4). pp. 211-213.

Chaudhary, Narendra and Majeed, Rubeena and Borker, Anupama (2011) Isolated cerebellar involvement in posterior reversible encephalopathty syndrome in a child with acute lymphobalstic leukemia. Indian Journal of Medical and Paediatric Oncology , 32 (4). pp. 211-213.

Chaudhary, Narendra and Borker, Anupama (2011) Chemotheraphy induced syndrome of inappropriate anti-diuretic hormone : A Potentially serious but reversible adverse event. PHO Bulletin, 4 (2). pp. 13-15.

Chaudhary, Narendra and Borker, Anupama (2011) Chemotherapy induced syndrome of inappropriate anti-diuretic hormone: A potentially serious but reversible adverse event. PHO Bulletin, 4 (2). pp. 13-15.

Kini, Kiran and Chopra, Deepti and Kini, Pushpa (2011) Factor XIII deficiency in siblings: Importance of prophylactic replacement. Indian Journal of Hematology and Blood Transfusion, 27 (3). pp. 180-182.

Borker, Anupama and Choudhary, Narendra (2011) Rituximab. Indian Pediatrics, 48. pp. 627-632.

Pais, Maria and Devi, Elsa Sanatombi and Pai, Muralidhar V and Lewis, Leslie and Gorge, Anice and Mayya, Shreemathi S and Bairy, KL (2011) A descriptive study on the neonatal sepsis, bacterial isolates and antibiotic susceptibility patterns among neonates. International Journal of Community Pharmacy, 4 (2). pp. 19-24.

Nayak, Dinesh M and Kumar, Naveen and Bhaskaranand, Nalini and Nayak, Chandrika (2011) Bacterial Profile of the Oropharynx in Infants: An Assessment of the Confounding Factors for Colonization. Indian Journal of Pediatrics, 78 (7). pp. 807-811.

Kamath, Madhav and Nayak, Dinesh and Nayak, Chandrika D (2011) A Rare Case of Primary Polydipsia in a Child. Pediatric Oncall, 8.

Chaudhary, Narendra and Borker, Anupama (2011) Solitary Skeletal Lesion as Primary Manifestation of Burkitt's lymphoma in a Child : A Rare Presentation. PHO Bulletin, 4 (1). pp. 3-4.

Chaudhary, Narendra and Borker, Anupama (2011) Solitary Skeletal Lesion as Primary Manifestation of Burkitt’s lymphoma in a Child: A Rare Presentation. PHO Bulletin, 4 (1). pp. 3-4.

Saadi, Abdul Vahab and Girisha, KM and Puthiya, Gopinath M and Satyamoorthy, K (2011) Analysis of cosegregation of intragenic DNA sequence variations as markers of maternal cell contamination in prenatal diagnosis of beta thalassemia. Translational Research, 157 (3). pp. 150-155. (Submitted)

Bhat, YR and Vinayaka, G and Vani, R and Prashanth, KA and Sreelakshmi, K (2011) Antenatal Bartter syndrome: A Rare cause of Unexplained Severe Polyhydramnios. Annals of Tropical Paediatrics, 31. pp. 153-157.

Bhat, Ramesh Y and Lewis, Leslie and Vandana, KE (2011) Bacterial Isolates of Early-onset NeonatalSepsis and their Antibiotic Susceptibility pattern between 1998 and 2004: an audit from a center in India. Italian Journal of Pediatrics.

Ramesh Bhat, Y and Lewis, Leslie and Vandana, KE (2011) Bacterial isolates of early-onset neonatal sepsis and their antibiotic susceptibility pattern between 1998 and 2004: an audit from a center in India. Italian Journal of Pediatrics.

Mundkur, Suneel C and Ramesh, B and Lewis, Leslie (2011) Coagulase negative staphylococcus (CONS) infection in neonatal lCU. WebmedCentral, 2 (12). pp. 2-12. ISSN 2046-1690

Bhat, Ramesh Y and Baby, Lincy P (2011) Early Onset of Neonatal Sepsis: Analysis of the Risk Factors and the Bacterial Isolates by Using the BacT Alert System. Journal of Clinical and Diagnostic Research., 5 (7). pp. 1385-1388.

Borker, Anupama (2011) The Emperor of All Maladies: A Biography of Cancer by Siddharta Mukherjee. PHO Bulletin, 4 (2). pp. 18-19.

Meikandan, Kavitha and Hebbar, Shrikiran and Mundkur, Suneel C (2011) Empty sella syndrome with panhypopituitarism ani> peripiieral pulmonar'r stenosis• a rare co•existence. Pediatric Oncall, 8 (3). pp. 1-2. ISSN 0973-0958

Girisha, KM and Thanvanthri, Gururajan Vasudevan and Saadi, Abdul Vahab and Shah, Hitesh and Puthiya, Gopinath M and Satyamoorthy, K (2011) Hypoplasia/aplasia of pelvis, femora, fibulae, ulna, digits and nails: Fuhrmann syndrome without WNT7A mutations. Clinical Dysmorphology, 20 (4). pp. 205-209.

Shweta, C and Mundkur, Suneel C and Varma, Chaitanya PV (2011) Knowledge and beliefs about HIV/AIDS among adolescents. WebmedCentral, 2 (12). pp. 2-6. ISSN 2046-1690

Varma, Chaitanya PV and Hebbar, Shrikiran and Mundkur, Suneel C and Karthick, A (2011) Multiple cafe au lait spots. WebmedCentral PAEDIATRICS, 2 (12). pp. 1-3. ISSN 2046-1690

Chaudhary, N and Borker, A (2011) Pleural Rhabdomyosarcoma: A rare entity. Indian Journal of Cancer, 48 (2).

Mundkur, Suneel C and Swaminathan, N and Lewis, Leslie (2011) A Possibile role of Antenatal Vitamin K Administration in Preventing Epiphyseal Stippling in Fetal Hydantoin Syndrome. WebmedCentral, 2 (12). pp. 1-4. ISSN 2046-1690

Kodandapani, Sreelakshmi and Pai, Muralidhar V and Kumar, Vijay and Pai, Kanthilatha V (2011) Prenatal Diagnosis of CongenitalMesenchymal Hamartoma of Liver: A Case Report. Case Reports in Obstetrics and Gynecology, 2011. pp. 1-3.

Khanna, Vinay and Khanna, Ruchee and Hebbar, Shrikiran and Shashidhar, V and Mundkur, Suneel C and Munim, Frenil and Annamalai, Karthick and Nayak, Deepak M and Mukhopadhayay, Chiranjay (2011) Primary Amoebic meningoencephalitis in an infant due to naegleria fowleri. Case Reports in Neurological Medicine, 2011. pp. 1-3.

Khanna, Vinay and Khanna, Ruchee and Hebbar, Shrikiran and Shashidhar, V and Mundkur, Suneel C and Munim, Frenil and Annamalai, Karthick and Nayak, Deepak and Mukhopadhayay, Chiranjay (2011) Primary moebic meningoencephalitis in an infant due to naegleria fowleri. Case Reports in Neurological Medicine, 2011. pp. 1-3.

Shah, Hitesh and Singh, Gurinder and Vijayan, Sandeep and Girisha, KM (2011) Second Report of Slipped Capital Femoral Epiphysis in Rubinstein–Taybi Syndrome. Clinical Dysmorphology, 20 (1). (Submitted)

Borker, Anupama and Chaudhary, Narendra (2010) Optimal supportive care. Hematology Update, 1. pp. 31-33.

Chaudhary, Narendra and Borker, Anupama (2010) Aleukemic Leukemia Cutis In A Patient With Pre-B Acute Lymphoblastic Leukemia. PHO Bulletin, 3 (2). p. 15.

Borker, Anupama (2010) InPOG : A Vision waiting to be fulfilled. PHO Bulletin, 3 (2). p. 3.

Kamath, Ganesh S and Borkar, Shirish and Chauhan, Aman and Bedjirgi, Chidanand and Kashyap, Nitin and Warrier, Raj (2010) Isolated Cervical Rib Fracture. Annals of Thoracic Surgery, 89 (6). e41-2.

Borker, Anupama and Chaudhary, Narendra (2010) Molecularly targeted therapy: Demethylating agents. Acute Myeloid Leukaemia. pp. 164-168.

Kamath, Ganesh S and Borkar, Shirish and Chauhan, Aman and Chidanand, Bedjirgi and Kashyap, Nitin and Warrier, Raj (2010) A Rare Case of Congenital Diaphragmatic Hernia With Ectopic Liver and Absent Pericardium. Annals of Thoracic Surgery , 89 (5). e36-37.

Chopra, D and Kini, Pushpa and Bhaskaranand, Nalini and Hebbar, Shrikiran (2010) Spectrum of infections in children with nephrotic syndrome. International Journal of Infectious Diseases, 14 (1). e419-e419.

Nayak, Dinesh (2010) Congenital Giant Aneurysm of the Mid-Portion of Basilar Artery. Pediatric Oncall, 7 (1).

Bhat, Ramesh Y and Swaminathan, Nithya and Kalwaje, Vandana E (2010) Alcaligenes Meningitis in a Neonate. Journal of Pediatric Infectious Diseases, 5. pp. 297-298.

Girisha, KM and Rajasekhar, M and Gopinath, PM and Satyamoorthy, K (2010) Balanced Translocation in Mother Leading to Interchange Trisomy 21? Genetic Counseling, 21 (2). pp. 183-185.

Bhat, Ramesh Y and Rao, Ashutosh (2010) Candida Arthritis of a Hip Joint in a Neonate. Journal of Pediatric Infectious Diseases, 5 (3). pp. 303-304.

Girisha, KM and Saadi, Abdul Vahab and Dalal, Ashwin B and Gopinath, PM and Satyamoorthy, K (2010) Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis. Ann Hematol, 89. pp. 625-626.

Girisha, KM and Lewis, Leslie and Phadke, Shubha R and Kutsche, Kerstin (2010) Costello Syndrome With Severe Cutis Laxa and Mosaic HRAS G12S Mutation. American Journal of Medical Genetics. pp. 2861-2864.

Bhat, Ramesh Y (2010) Epidermolysis Bullosa Simplex. JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 15 (4). pp. 3215-3216.

Borker, Anupama and Chaudhary, Narendra (2010) Hodgkin lymphoma : Classification. Hodgkin Lymphoma. pp. 8-10.

Lewis, Leslie and Bhat, Ramesh Y and Naik, Prashant and Sethi, Kanchan and Girisha, KM (2010) Opsismodysplasia. Indian J Pediatr, 77 (5). pp. 567-568. (Submitted)

Bhat, Ramesh Y and Rao, Amitha (2010) The Performance of Haematological Screening Parameters and CRP in Early Onset Neonatal Infections. Journal of Clinical and Diagnostic Research, 4 (6). pp. 3331-3336.

Bhat, Ramesh Y and Vinayak , G and Sushma , S (2010) Systemic allergic reaction to a caterpillar in a 3-month-old infant. Annals of Tropical Paediatrics, 30 (1). pp. 83-86.

Bhat, R (2010) Twin to Twin Transfusion Syndrome. Kathmandu University Medical Journal, 8 (29). pp. 87-90.

Girisha, KM and Bhat, PV and Adiga, PK and Pai, AH and Rai, Lavanya (2010) Unusual Facial Cleft in Fryns Syndrome: Defect of Stomodeum? Genetic Counseling, 21 (2). pp. 233-236.

Airody, Karanth Sathyajith and Goneppanavar, Umesh and Rao, Shwethapriya and Rao, Aroor Amitha (2009) Beware of external tracheal compression in children with acute onset stridor. Pediatric Anesthesia, 19 (5). pp. 542-544.

Saadi, Abdul Vahab and Sen, Supratim and Ravindran, Nivedita and Mony, Sridevi and Mathew, Anila and Vijayan, Neetha and Nayak, Geetha and Bhaskaranand, Nalini and Banerjee, Moinak and Satyamoorthy, K (2009) Analysis of Genotype and Haplotype Effects of ABCB1 (MDR1) Polymorphisms in the Risk of Medically Refractory Epilepsy in an Indian Population. Drug Metab. Pharmacokinet., 24 (3). pp. 255-260.

Saadi, Abdul Vahab and Sen, Supratim and Ravindran, Nivedita and Mony, Sridevi and Nayak, Geetha and Bhaskaranand, Nalini and Satyamoorthy, K (2009) Analysis of Genotype and Haplotype Effects of ABCB1 (MDR1) Polymorphisms in the Risk of Medically Refractory Epilepsy in an Indian Population. Drug metabolism and pharmacokinetics, 24 (3). pp. 255-260.

Girisha, KM and Ganesh, HK and Rao, Lakshmi and Srilatha, PS (2009) Massive Cranial Osteolysis, Skin Changes, Growth Retardation and Developmental Delay: Gorham Syndrome With Systemic Manifestations? American Journal of Medical Genetics, 152A. pp. 759-763.

Bhat, RY and Kumar, V (2009) Neonatal Teratoma. JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 3 (5). pp. 1792-1794.

Bhat, Ramesh Y and Prakashini, K (2009) A Neonate With Multiple Fractures. JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 3. pp. 1326-1328.

Bhat, Ramesh Y and Kumar, N (2009) Outcome Of Sepsis Evaluations In Very-Low-Birth-Weight Premature Neonates. Journal of Clinical and Diagnostic Research, 3 (6). pp. 1847-1852.

Bhat, YR and Gupta, BK (2009) A Pre-Auricular Solitary Tuberculous Ulcer. Journal of Clinical and Diagnostic Research., 3 (3). pp. 1569-1572.

Sonkusare, S and Rai, Lavanya and Naik, P (2009) Preterm Birth: Mode of Delivery and Neonatal Outcome. Medical Journal of Malaysia, 64 (4). pp. 303-306.

Kini, Kiran and Kini, Pushpa (2009) Sleep deprivation for radiological procedures in children. Pediatric Radiology, 39. p. 1255.

Bhat, Ramesh Y and Prakashini, K and Sen, Supratim (2009) Subdural Effusion Complicating Neonatal Meningitis: Successful Treatment with Acetazolamide. Indian Journal of Pediatrics, 76. pp. 103-105.

Lewis, Leslie and Poojari, Ganesh and Sanoj, KM and Kamath, Sowmini P and Kachane, Yogesh P (2008) Neonatal Arrhythmia with Diaphragmatic Eventration. The Indian Journal of Pediatrics, 75 (10). pp. 1083-1085. ISSN 0019-5456

Lewis, Leslie and Sanoj, KM and Poojari, Ganesh and Kamath, Sowmini P (2008) Neonate Subcapsular Splenic Hematoma. Indian Journal of Pediatrics, 75 (9). pp. 950-952.

Bhat, RY and Rao, A and Althaf, * and Prakashini, K (2008) An evolved diagnosis of congenital tuberculosis in a very low birthweight premature neonate. International Journal of Tuberculosis and Lung Disease, 12 (3). pp. 344-345. ISSN 1027-3719

Bhat, Ramesh Y and Rao, Amitha (2008) Transcutaneous Bilirubin in Predicting Hyperbilirubinemia in Term Neonates. The Indian journal of pediatrics, 75 (2). pp. 119-123.

Bhat, YR and Kumar, V and Rao, A (2008) Congenital Diaphragmatic Hernia in a Developing Country. Singapore Medical Journal, 49 (9). pp. 715-718.

Hebbar, Shrikiran and Bhaskaranand, Nalini and Kini, Pushpa (2008) Enhanced Urinalysis in Febrile Children with Suspected Urinary Tract Infection. International Journal of Infectious Diseases. e80.

Nayak, Chandrika D and Nayak, Dinesh M and Annaswamy, Raja and Rao, Anjali (2008) Erythrocyte indicators of oxidative changes in patients with graded traumatic head injury. Neurol India, 56 (1). pp. 31-35.

Pandey, Deeksha and Pai, Murlidhar V and Nambiar, Jayaraman and Lewis, Leslie and Pandey, Vivek (2008) Gollop-Wolfgang Complex - A Rare Limb Deficiency Syndrome: Case Report And Review Of Literature. The Internet Journal of Gynecology and Obstetrics, 9 (1).

Bhat, YR and Abhishek, N (2008) Mainstream End-tidal Carbon Dioxide Monitoring in Ventilated Neonates. Singapore Med J, 49 (3).

Bhat, RY and Rao, A (2008) Meconium-stained Amniotic Fluid and Meconium Aspiration Syndrome: A Prospective Study. Annals of Tropical Paediatrics, 28. pp. 199-203.

Bhat, Ramesh Y and Cherian, Carol S (2008) Neonatal Thrombocytopenia Associated with Maternal Pregnancy Induced Hypertension. Indian Journal of Pediatrics, 75. pp. 571-573.

Bhat, Ramesh Y and Sen, Supratem (2008) A Neonate With Extended Spectrum and Thrombocytopenia. Townes-Brocks Syndrome, 29 (9). pp. 1337-1339.

Bhat, Ramesh Y and Venkatesh, KS (2008) Obstetric Practice Related Severe Neonatal Jaundice. JK Science, 10 (1). pp. 46-47.

Karthikeyan, Kadirvel and Sinha, Indrajit and Prabhu, Krishnananda and Bhaskaranand, Nalini and Rao, Anjali (2008) Plasma Protein Thiols and Total Antioxidant Power in Pediatric Nephrotic Syndrome. Nephron Clin Pract , 110. pp. 10-14.

Mundkur, Suneel C and Hebbar, Shrikiran and Bhaskaranand, Nalini and Kini, Pushpa and Sarma, M (2008) A study of serum C-Reactive Protein (CRP) at admission ,as a predictor of outcome in febrile children. International Journal of Infectious Diseases. e81.

Bhat, Ramesh Y and Rao, Amitha (2007) Glomerulocystic disease: a severe form in a monozygous twin. Annals of Tropical Paediatrics , 27 (3). pp. 237-240.

Nayak, Chandrika D and Nayak, Dinesh and Annaswamy, Raja and Rao, Anjali (2007) Time-Relative Changes in the Erythrocyte Antioxidant Enzyme Activities and their Relationship with Glasgow Coma Scale Scores in Severe Head Injury Patients in the 21-Day Posttraumatic Study Period. Indian Journal of Medical Sciences, 61 (7). pp. 381-389.

Bhat, Ramesh Y (2007) Management of Neonatal Hyperbilirubinemia- What is the Efficacy of Exchange Transfusion by Different Techniques? Journal of Neonatology , 21 (1). pp. 68-70.

Bhat, Ramesh Y (2007) Survival pattern among neonates requiring intensive care. Karnataka Paediatric Journal, 21 (1). pp. 9-14.

Cherian, Sumina and Jameson, Shiji and Rajarajeswari, Chitikineni and Vemuri, Helena and Lakshmi, Latha and Anu, Rekha MR and Nagamma, T and Raju, Subba V and Kini, Pushpa G and Rao, Anjali (2007) Oxidative stress in sepsis in children. Indian Journal of Medical Research, 125 (2). pp. 143-148.

Bhat, Ramesh Y (2007) Pneumoperitoneum in a newborn. Indian Journal of Practical Pediatrics, 9 (3). pp. 242-244.

Nayak, Chandrika and Nayak, Dinesh and Annaswamy, Raja and Rao, Anjali (2007) Relationship between Markers of Lipid Peroxidation, Thiol Oxidation and Glasgow Coma Scale Scores of Moderate Head Injury Patients in the 7 day Post-Traumatic Period. Neurological Research.

Bhat, Ramesh Y (2007) Renal Subcapsular Abscess. Indian Pediatrics, 44. pp. 546-547.

Bhat, RY and Rao, A and Muthuram, * (2006) Cantrell syndrome in one of a set of monozygotic twins. Singapore Medical Journal, 47 (12). pp. 1087-1088.

Bhat, Ramesh Y (2006) Transient Diabetes Mellitus in a Newborn -Near Fatal Case. Journal of Neonatology , 20 (3). pp. 280-283.

Nayak, Chandrika and Nayak, Dinesh and Raja, Annaswamy and Rao, Anjali (2006) Time-level relationship between indicators of oxidative stress and Glasgow Coma Scale scores of severe head injury patients. Clin Chem Lab Med , 44 (4). pp. 460-463.

Bhat, Ramesh Y (2005) Neonatal Resuscitation Guidelines major changes to 2005. Karnataka Paediatric Journal, 19 (4). pp. 9-10.

Bhat, Ramesh Y and Shenoy, Sangeetha (2005) Pseudosyndactyly in Amniotic Band Syndrome a Brief Report. Journal of Neonatology, 19 (3). p. 252.

Bhat, Ramesh Y and Sanoj, KM (2005) Sclerocornea. Indian Pediatrics, 42. p. 277.

Girisha, KM and Nayak, Shalini S and Shukla, Anju and Bhat, SK (2005) Alobar holoprosencephaly, cleft lip/palate, urorectal septum malformation sequence and congenital perineal hernia in a fetus. Genetic Counseling, 26 (3). pp. 321-325.

Hebbar, Shrikiran and Bairy, Indira and Bhaskaranand, Nalini and Upadhyaya, Santhosh and Sarma, Moinak Sen and Shetty, Anup Kumar (2005) Fatal case of Naegleria fowleri meningo-encephalitis in an infant: case report. Annals of Tropical Paediatrics, 25 (3). pp. 223-226.

Bhat, Ramesh Y (2004) Kangaroo Mother Care. Karnataka Paediatric Journal, 18.

Diwakar, KK and Bhat, Ramesh Y (2004) Thrombocytopenia in early neonataon period- Is Intravenous gamaglobulin useful? Journal of Neonatology, 18 (1).

Hebbar, Shrikiran and Upadyaya, S (2004) A Case of Enterococcal Meningitis in a Healthy Infant. The Internet Journal of Infectious Diseases, 4 (2). pp. 1-3.

Bhat, Ramesh Y (2004) Fibular Hemimelia With Four Ray Foot. Journal of Neonatology, 18 (4).

Bhat, Ramesh Y (2004) Natal teeth in 32 Week Preterm Neonate. Karnataka Paediatric Journal, 18 (1).

Pandit, Lekha and Kapadia, R and Kini, Pushpa and Rao, S (1994) Metachromatic Leukodystropy Presenting with Extrapyramidal Disturbances. Indian Pediatrics, 31 (6). pp. 690-694.

Kini, Pushpa and Baliga, Meera and Bhaskaranand, Nalini (1994) Severe derangem.ent of the coagulation profile following multiple bee stings in a 2-year-old boy. Annals of Tropical Paediatrics, 14 (2). pp. 153-155.

Kini, Pushpa G and Prabhakar, Paul and Baliga, Meera (1993) Bone changes in Herpes simplex infection mimicking congenital syphilis: case report. Annals of Tropical Paediatrics, 13. pp. 399-400.

Kini, Pushpa and Baliga, Meera (1993) Unusual presentation of cytomegaloviral infection in a 5-month-old baby: case report. Annals of Tropical Paediatrics, 13 (4). pp. 395-397.

Book Section

Girisha, KM (2015) Gene, Genome and Genetic Basis of Diseases. In: PG Textbook of Pediatrics. Jaypee Brothers Medical Publishers (P) Ltd, New Delhi, pp. 19-21. ISBN 978-93-5152-725-1

Girisha, KM (2015) Molecular genetics, human genome project and genomic medicine. In: API Textbook of Medicine. Jaypee Brothers Medical Publishers (P) Ltd, New Delhi, pp. 316-321. ISBN 978-93-5152-415-1

Girisha, KM (2015) Mucopolysaccharidoses. In: PG Textbook of Pediatrics. Jaypee Brothers Medical Publishers (P) Ltd, New Delhi, pp. 139-143. ISBN 978-93-5152-725-1

Girisha, KM Galactosemia. In: Treatment & Prognosis in Pediatrics. Jaypee Brothers, New Delhi, pp. 402-403.

Girisha, KM Gaucher Disease. In: Treatment & Prognosis in Pediatrics. Jaypee Brothers, New Delhi, pp. 404-405.

Conference or Workshop Item

Acharya, Dinesh U and Shirwaikar, Rudresh D and Makkithaya, Krishnamoorthi and RajanSurulivel, M and Lewis, Leslie (2016) Design and Development of a Real Time Data Mart for Neonatal Intensive Care Unit. In: International Conference on Recent Trends in Engineering and Material Sciences, 17/03/2016, Jaipur National University, Jaipur.

Mago, Nikhit and Srivastava, Shikhar and Shirwaikar, Rudresh D and Acharya, Dinesh U and Lewis, Leslie and Shivakumar, M (2016) Prediction of Apnea of Prematurity in Neonates using Support Vector Machines and Random Forests. In: International Conference on Contemporary Computing and Informatics, 14/12/2016, Amity University, Noida.

Ghoshal, Indranil and Prabhu, Krishnananda and Hebbar, Shrikiran (2014) Renal tubular acidosis with extreme hypercalcemia- a case report. In: South Regional Conference of the Association of Clinical Biochemists of India, 23-24 May 2014, Kodailbail, Mangalore. (Submitted)

John, Pamala and Mohapatra, Nirupam and Prasad, Anushre and Hebbar, Shrikiran and Rao, Pragna (2013) A case report on mucopolysaccharidosis-hunters disease. In: International conference on Inborn Errors of Metabolism & 2nd National Conference of ISIEM, 6th April 2013, New Delhi, India. (Submitted)

This list was generated on Fri Apr 28 19:03:15 2017 UTC.