Showing results (11-20 of 47) with videos related to
Sort By:
Pageof 5
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 GrewalCase Reports in Neurology|October 17, 2018
Limb Girdle Muscular Dystrophy due to Digenic Inheritance of <i>DES</i> and <i>CAPN3</i> MutationsLeema Reddy Peddareddygari, Kinsi Oberoi, Raji P GrewalThe 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 GrewalThe 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 GrewalActa 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 GrewalJournal of Clinical Neuromuscular Disease|May 29, 2019
Adult Diagnosis of Type 1 Fiber Predominance Myopathy Caused by Novel Mutations in the RYR1 GeneLeema Reddy Peddareddygari, Kinsi Oberoi, Leroy R Sharer, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 21, 2004
Clinical and genetic analysis of a family with PROMMRaji P Grewal, Shanxiang Zhang, Wei Ma, et al.Case Reports in Neurology|July 28, 2016
Factors Affecting Phenotype Variability in a Family with CMT2B: Gender and LRSAM1 GenotypeLeema Reddy Peddareddygari, Kinsi Oberoi, Jaasrini Reddy Vellore, et al.Journal of the Neurological Sciences|May 27, 2006
Clinicopathologic and genetic analysis of siblings with NF1 and adult-onset gliomasSubramanian Hariharan, John E Donahue, Cecial Garre, et al.Journal of Clinical Neuromuscular Disease|May 26, 2018
Novel Mutation in Anoctamin 5 Gene Causing Limb-Girdle Muscular Dystrophy 2LLeema Reddy Peddareddygari, Kinsi Oberoi, Ada Baisre-De Leon, et al.Pageof 5