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Indian Pediatrics|June 27, 2009
Carbonic anhydrase II deficiency a novel mutationSheela Nampoothiri, Yair AniksterNephron. Physiology|August 19, 2011
Familial autosomal recessive renal tubular acidosis: importance of early diagnosisAsaf Vivante, Danny Lotan, Naomi Pode-Shakked, et al.The Indian Journal of Radiology & Imaging|April 16, 2016
Prenatal detection of congenital high airway obstruction syndrome with encephaloceleLaxmi Devi Padmanabhan, Sheela NampoothiriPediatric Endocrinology Reviews : PER|December 20, 2005
Optic neuropathies in inherited metabolic disordersMarjan Huizing, Brian P Brooks, Yair AniksterMolecular Genetics and Metabolism|October 1, 2005
Optic atrophies in metabolic disordersMarjan Huizing, Brian P Brooks, Yair AniksterIndian Journal of Human Genetics|November 20, 2012
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutationKarippoth Mohandas Nair, Peter Lohse, Sheela NampoothiriIndian Journal of Ophthalmology|November 18, 2016
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease managementSathya Priya, Sheela Nampoothiri, Parveen Sen, 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.Pageof 30