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Journal of Molecular Neuroscience : MN|June 9, 2021
A Novel L1 Linker Mutation in DES Resulted in Total Absence of ProteinRashmi Santhoshkumar, Veeramani Preethish-Kumar, Kiran Polavarapu, et al.Annals of Indian Academy of Neurology|July 2, 2020
Palliative Care Needs and Care Giver Burden in Neurodegenerative Diseases: A Cross Sectional StudyZacharias Lithin, Priya T Thomas, G Manjusha Warrier, et al.Annals of Indian Academy of Neurology|September 15, 2017
Detection of Dysferlin Gene Pathogenic Variants in the Indian Population in Patients Predicted to have a Dysferlinopathy Using a Blood-based Monocyte Assay and Clinical Algorithm: A Model for Accurate and Cost-effective DiagnosisRashna Sam Dastur, Pradnya Satish Gaitonde, Munira Kachwala, et al.Journal of Human Genetics|March 13, 2021
Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndromeMainak Bardhan, Kiran Polavarapu, Nandeesh N Bevinahalli, et al.Internal Medicine Journal|August 14, 2023
Clinical spectrum, biochemical profile and disease progression of Kennedy disease in an Indian cohortDipti Baskar, Preethish Veeramani-Kumar, Kiran Polavarapu, et al.The Lancet Regional Health. Western Pacific|September 29, 2025
Pan-Asian consortium for treatment and research in ALS (PACTALS) guidelines for management of amyotrophic lateral sclerosisSteve Vucic, Nortina Shahrizaila, Osamu Kano, et al.Pageof 2