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Sheela Nampoothiri

Showing results (1-10 of 168) with videos related to

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Indian Pediatrics|June 27, 2009
Carbonic anhydrase II deficiency a novel mutationSheela Nampoothiri, Yair Anikster
The Indian Journal of Radiology & Imaging|April 16, 2016
Prenatal detection of congenital high airway obstruction syndrome with encephaloceleLaxmi Devi Padmanabhan, Sheela Nampoothiri
Circulation|June 11, 2008
Images in cardiovascular medicine. Arterial tortuosity syndrome: phenotypic features and cardiovascular manifestationsGayathri Satish, Sheela Nampoothiri, Mahesh Kappanayil
Indian Journal of Human Genetics|November 20, 2012
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutationKarippoth Mohandas Nair, Peter Lohse, Sheela Nampoothiri
Indian Journal of Ophthalmology|November 18, 2016
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease managementSathya 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 phenotypeSmrithi Salian, Sheela Nampoothiri, Anju Shukla, et al.
Indian Journal of Pediatrics|February 18, 2011
Fanconi-Bickel syndromeMohandas Nair K, Osamu Sakamoto, Sujatha Jagadeesh, et al.
Pediatric Dermatology|July 27, 2010
Nevus comedonicus syndrome--nevus comedonicus associated with ipsilateral polysyndactyly and bilateral oligodontiaFeroze Kaliyadan, Sheela Nampoothiri, V Sunitha, et al.
Indian Journal of Pediatrics|November 30, 2013
Recurrence of Angelman syndrome in siblings: challenges in genetic counselingDhanya Yesodharan, M V Thampi, Teena Koshy, et al.
Indian Pediatrics|November 15, 2011
Lipoprotein lipase deficiency in an infantSheela Nampoothiri, Natasha Radhakrishnan, Andrea Schwentek, et al.
Pageof 17

Showing results (1-10 of 168) with videos related to

Sort By:
Pageof 17
Indian Pediatrics|June 27, 2009
Carbonic anhydrase II deficiency a novel mutationSheela Nampoothiri, Yair Anikster
The Indian Journal of Radiology & Imaging|April 16, 2016
Prenatal detection of congenital high airway obstruction syndrome with encephaloceleLaxmi Devi Padmanabhan, Sheela Nampoothiri
Circulation|June 11, 2008
Images in cardiovascular medicine. Arterial tortuosity syndrome: phenotypic features and cardiovascular manifestationsGayathri Satish, Sheela Nampoothiri, Mahesh Kappanayil
Indian Journal of Human Genetics|November 20, 2012
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutationKarippoth Mohandas Nair, Peter Lohse, Sheela Nampoothiri
Indian Journal of Ophthalmology|November 18, 2016
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease managementSathya 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 phenotypeSmrithi Salian, Sheela Nampoothiri, Anju Shukla, et al.
Indian Journal of Pediatrics|February 18, 2011
Fanconi-Bickel syndromeMohandas Nair K, Osamu Sakamoto, Sujatha Jagadeesh, et al.
Pediatric Dermatology|July 27, 2010
Nevus comedonicus syndrome--nevus comedonicus associated with ipsilateral polysyndactyly and bilateral oligodontiaFeroze Kaliyadan, Sheela Nampoothiri, V Sunitha, et al.
Indian Journal of Pediatrics|November 30, 2013
Recurrence of Angelman syndrome in siblings: challenges in genetic counselingDhanya Yesodharan, M V Thampi, Teena Koshy, et al.
Indian Pediatrics|November 15, 2011
Lipoprotein lipase deficiency in an infantSheela Nampoothiri, Natasha Radhakrishnan, Andrea Schwentek, et al.
Pageof 17