Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Cureus|November 23, 2022
Novel Titin Gene Mutation Causing Autosomal Dominant Limb-Girdle Muscular DystrophyLeema Reddy Peddareddygari, Kinsi Oberoi, Raji P Grewal
Case Reports in Neurological Medicine|October 14, 2014
Congenital insensitivity to pain: a case report and review of the literatureLeema Reddy Peddareddygari, Kinsi Oberoi, Raji P Grewal
Journal of Community Hospital Internal Medicine Perspectives|August 28, 2020
Complicated SPG4 presenting with recurrent urinary tract infectionKinsi Oberoi, Kabir S Grewal, Leema Reddy Peddareddygari
Case 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 Grewal
Case Reports in Neurology|September 5, 2020
A Novel Duplication Mutation in the <i>Myelin Protein Zero</i> Gene Causing Mild, Nonprogressive Demyelinating NeuropathyKinsi Oberoi, Alam S Grewal, Leema Reddy Peddareddygari
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|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.
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 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 1