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JCEM Case Reports|September 29, 2025
Late Diagnosis of Prader-Willi Syndrome in an Adolescent With Significant Complications of Type 2 DiabetesAlyssa Kahane, Emma Metivier, Allison Bahm, et al.Brain & Development|September 18, 2003
The floppy infant: contribution of genetic and metabolic disordersAsuri N Prasad, Chitra PrasadIndian Journal of Pediatrics|May 22, 2002
Genetics and cardiac anomalies: the heart of the matterChitra Prasad, Albert E ChudleyBrain & Development|September 13, 2011
Pyruvate dehydrogenase deficiency and epilepsyChitra Prasad, Tony Rupar, Asuri N PrasadRheumatology International|May 10, 2023
A survey of Canadian adult rheumatologists' knowledge, comfort level, and barriers in assessing psychosocial needs of young adults with rheumatic diseasesMadhavi Prasad, Michelle Batthish, Karen Beattie, et al.Journal of Pediatric Hematology/Oncology|November 12, 2024
Hepatoblastoma in a 13-Month-old Male With Oculofaciocardiodental SyndromeKriti Kumar, Chitra Prasad, Diana Masse, et al.Acta Paediatrica (Oslo, Norway : 1992)|March 1, 2011
Asymptomatic critical hypoglycaemia: a dangerous presentation of glycogen storage disease type Ib in infancyDirk E Bock, Charles A Rupar, Chitra PrasadAnnals of Indian Academy of Neurology|August 8, 2024
Severe Developmental Delay and Behavior Abnormalities in a Patient with De Novo CAMK2B Mutation: A Case Report and Literature ReviewKatherynn K Zhang, Charles A Rupar, Chitra PrasadMolecular Genetics and Metabolism|November 14, 2012
Severe phenotypic spectrum of mevalonate kinase deficiency with minimal mevalonic aciduriaChitra Prasad, Marina I Salvadori, C A RuparPageof 11