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Neurology International|February 28, 2022
Clinical and Genetic Analysis of a Patient with CMT4JLeema Reddy Peddareddygari, Raji P GrewalCase Reports in Neurology|August 11, 2022
Intrafamilial Phenotypic Variability Associated with the I1739V Mutation in the SCN9A GeneLeema Reddy Peddareddygari, Raji P GrewalCureus|May 6, 2024
A Patient With Charcot-Marie-Tooth Disease Type 4C (CMT4C) Presenting With Muscle Fasciculations and Motor NeuropathyLeema Reddy Peddareddygari, Raji P GrewalCase Reports in Genetics|June 12, 2015
Identification of Novel Mutations in Spatacsin and Apolipoprotein B Genes in a Patient with Spastic Paraplegia and HypobetalipoproteinemiaLeema Reddy Peddareddygari, Raji P GrewalJournal of Community Hospital Internal Medicine Perspectives|October 23, 2023
Demyelinating Peripheral Neuropathy Caused by the p.R160H Mutation in the <i>LITAF</i> GeneLeema Reddy Peddareddygari, 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 PeddareddygariCureus|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 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 PeddareddygariPageof 3