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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 GrewalJournal of Medical Case Reports|June 9, 2016
Focal seizures in a patient with myotonic disorder type 2 co-segregating with a chloride voltage-gated channel 1 gene mutation: a case reportLeema Reddy Peddareddygari, Arman Singh Grewal, Raji Paul 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.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.Case Reports in Medicine|September 4, 2010
Kikuchi-fujimoto disease associated with myasthenia gravis: a case reportOlukayode Onasanya, David Nochlin, Victor Casas, et al.World Journal of Oncology|October 7, 2017
Positive Germline Selection in Pedigrees With Multiple Endocrine Neoplasia Type 2 Carrying V804M Mutation in the RET GeneLeema Reddy Peddareddygari, Angela Musial Fay, Alexander L Shifrin, et al.Pageof 3