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Case Reports in Genetics|October 18, 2012
MOMO Syndrome with Holoprosencephaly and Cryptorchidism: Expanding the Spectrum of the New Obesity SyndromeSheetal Sharda, Inusha Panigrahi, Ram Kumar MarwahaBMJ Case Reports|July 4, 2012
Hemifacial microsomia with pulmonary hypoplasiaInusha Panigrahi, Rashmi Ranjan Das, Ram Kumar MarwahaJournal of Pediatric Endocrinology & Metabolism : JPEM|June 12, 2013
Lissencephaly presenting with congenital hypothyroidismSuresh Kumar, Renu Suthar, Inusha Panigrahi, et al.Pediatric Neurology|September 23, 2008
Neurofibromatosis type 1 with intracranial hemorrhage and horseshoe kidneyKana Ram Jat, Ram Kumar Marwaha, Inusha Panigrahi, et al.Indian Journal of Pediatrics|December 17, 2009
Seckel syndrome with chromosomal 18 deletionInusha Panigrahi, Satvinder Kaur, Ketan Kulkarni, et al.Indian Journal of Human Genetics|September 11, 2013
Proteus syndrome: Clinical profile of six patients and review of literatureSuresh Kumar Angurana, Renu Suthar Angurana, Inusha Panigrahi, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|September 14, 2013
Zellweger syndrome: prenatal and postnatal growth failure with epiphyseal stipplingSuresh Kumar, Renu Suthar, Sheetal Sharda, et al.Indian Journal of Pediatrics|November 12, 2009
Pediatric disorders of sex developmentKetan Prasad Kulkarni, Inusha Panigrahi, Reena Das, et al.Journal of Bone and Mineral Metabolism|February 5, 2010
Response to zolendronic acid in children with type III osteogenesis imperfectaInusha Panigrahi, Rashmi Ranjan Das, Sheetal Sharda, et al.Pageof 17