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Indian Pediatrics
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June 27, 2009
Carbonic anhydrase II deficiency a novel mutation
Sheela Nampoothiri, Yair Anikster
The Indian Journal of Radiology & Imaging
|
April 16, 2016
Prenatal detection of congenital high airway obstruction syndrome with encephalocele
Laxmi Devi Padmanabhan, Sheela Nampoothiri
Circulation
|
June 11, 2008
Images in cardiovascular medicine. Arterial tortuosity syndrome: phenotypic features and cardiovascular manifestations
Gayathri Satish, Sheela Nampoothiri, Mahesh Kappanayil
Indian Journal of Human Genetics
|
November 20, 2012
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutation
Karippoth Mohandas Nair, Peter Lohse, Sheela Nampoothiri
Indian Journal of Ophthalmology
|
November 18, 2016
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
Sathya Priya, Sheela Nampoothiri, Parveen Sen, et al.
Congenital Anomalies
|
April 29, 2018
Further evidence for causation of ischiospinal dysostosis by a pathogenic variant in BMPER and expansion of the phenotype
Smrithi Salian, Sheela Nampoothiri, Anju Shukla, et al.
Indian Journal of Pediatrics
|
February 18, 2011
Fanconi-Bickel syndrome
Mohandas Nair K, Osamu Sakamoto, Sujatha Jagadeesh, et al.
Pediatric Dermatology
|
July 27, 2010
Nevus comedonicus syndrome--nevus comedonicus associated with ipsilateral polysyndactyly and bilateral oligodontia
Feroze Kaliyadan, Sheela Nampoothiri, V Sunitha, et al.
Indian Journal of Pediatrics
|
November 30, 2013
Recurrence of Angelman syndrome in siblings: challenges in genetic counseling
Dhanya Yesodharan, M V Thampi, Teena Koshy, et al.
Indian Pediatrics
|
November 15, 2011
Lipoprotein lipase deficiency in an infant
Sheela Nampoothiri, Natasha Radhakrishnan, Andrea Schwentek, et al.
Page
of 17
Search research articles
Search
Showing results (1-10 of 168) with videos related to
Sort By:
Page
of 17
Indian Pediatrics
|
June 27, 2009
Carbonic anhydrase II deficiency a novel mutation
Sheela Nampoothiri, Yair Anikster
The Indian Journal of Radiology & Imaging
|
April 16, 2016
Prenatal detection of congenital high airway obstruction syndrome with encephalocele
Laxmi Devi Padmanabhan, Sheela Nampoothiri
Circulation
|
June 11, 2008
Images in cardiovascular medicine. Arterial tortuosity syndrome: phenotypic features and cardiovascular manifestations
Gayathri Satish, Sheela Nampoothiri, Mahesh Kappanayil
Indian Journal of Human Genetics
|
November 20, 2012
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutation
Karippoth Mohandas Nair, Peter Lohse, Sheela Nampoothiri
Indian Journal of Ophthalmology
|
November 18, 2016
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
Sathya Priya, Sheela Nampoothiri, Parveen Sen, et al.
Congenital Anomalies
|
April 29, 2018
Further evidence for causation of ischiospinal dysostosis by a pathogenic variant in BMPER and expansion of the phenotype
Smrithi Salian, Sheela Nampoothiri, Anju Shukla, et al.
Indian Journal of Pediatrics
|
February 18, 2011
Fanconi-Bickel syndrome
Mohandas Nair K, Osamu Sakamoto, Sujatha Jagadeesh, et al.
Pediatric Dermatology
|
July 27, 2010
Nevus comedonicus syndrome--nevus comedonicus associated with ipsilateral polysyndactyly and bilateral oligodontia
Feroze Kaliyadan, Sheela Nampoothiri, V Sunitha, et al.
Indian Journal of Pediatrics
|
November 30, 2013
Recurrence of Angelman syndrome in siblings: challenges in genetic counseling
Dhanya Yesodharan, M V Thampi, Teena Koshy, et al.
Indian Pediatrics
|
November 15, 2011
Lipoprotein lipase deficiency in an infant
Sheela Nampoothiri, Natasha Radhakrishnan, Andrea Schwentek, et al.
Page
of 17