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Frontiers in Immunology|November 22, 2021
Bruton's Tyrosine Kinase (BTK) Inhibitors and Autoimmune Diseases: Making Sense of BTK Inhibitor Specificity Profiles and Recent Clinical Trial Successes and FailuresGarth E Ringheim, Matthew Wampole, Kinsi OberoiCureus|November 23, 2022
Novel Titin Gene Mutation Causing Autosomal Dominant Limb-Girdle Muscular DystrophyLeema Reddy Peddareddygari, Kinsi Oberoi, Raji P GrewalCase 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 GrewalJournal of Community Hospital Internal Medicine Perspectives|August 28, 2020
Complicated SPG4 presenting with recurrent urinary tract infectionKinsi Oberoi, Kabir S Grewal, Leema Reddy PeddareddygariCase 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 GrewalCase 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 PeddareddygariCase 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 PeddareddygariJournal 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