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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 22, 2003
X-linked Charcot-Marie-Tooth disease caused by a novel point mutation in the connexin-32 geneW Ma, M Farrukh Nizam, R P Grewal
Case Reports in Neurology|March 9, 2018
Clinical and Genetic Analysis of an Asian Indian Family with Charcot-Marie-Tooth Disease Type 4CRaji P Grewal, Kinsi Oberoi, Leema Reddy Peddareddygari
Journal of Clinical Neuromuscular Disease|March 10, 2011
Limb-girdle muscular dystrophy type 2A resulting from homozygous G2338C transversion mutation in the calpain-3 geneLeema Reddy Peddareddygari, Victoria Surgan, Raji P Grewal
Case Reports in Neurology|October 17, 2018
Limb Girdle Muscular Dystrophy due to Digenic Inheritance of DES and CAPN3 MutationsLeema Reddy Peddareddygari, Kinsi Oberoi, Raji P Grewal
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 30, 2007
Possible anticipation in hereditary spastic paraplegia type 4 (SPG4)P Leema Reddy, William K Seltzer, Raji P Grewal
The International Journal of Neuroscience|August 20, 2014
A familial form of benign paroxysmal positional vertigo maps to chromosome 15Martin S Gizzi, Leema Reddy Peddareddygari, Raji P Grewal
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 19, 2021
Genotype phenotype analysis in a family carrying truncating mutations in the titin geneLeema Reddy Peddareddygari, Ada Baisre-de León, Raji P Grewal
Indian Journal of Ophthalmology|April 1, 1992
Spontaneous extrusion of cysticercosis: report of three casesR K Bansal, A Gupta, S P Grewal, et al.
Scandinavian Cardiovascular Journal : SCJ|October 12, 1999
Surgical repair of type B aortic dissection complicated by early postoperative lung vein and artery thrombosisS Thelin, S Karacagil, P Grewal, et al.
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