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Neurology India|March 5, 2024
Myotonic Dystrophy Type 1 (DM1): Clinical Characteristics and Disease Progression in a Large CohortTanushree Chawla, Nishanth Reddy, Rahul Jankar, 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.European Journal of Neurology|October 30, 2020
Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutationsShamita Sanga, Arnab Ghosh, Krishna Kumar, 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.Clinical Genetics|January 7, 2026
A Homozygous CPSF1 Variant Causes Congenital Cataract, Intellectual Disability and HyperphagiaOzge Aksel Kilicarslan, Andrea Gangfuß, Andreas Hentschel, et al.Neurological Research and Practice|October 9, 2022
PET-MRI in idiopathic inflammatory myositis: a comparative study of clinical and immunological markers with imaging findingsManu Santhappan Girija, Ravindu Tiwari, Seena Vengalil, et al.Journal of Clinical Ultrasound : JCU|October 5, 2021
Diaphragmatic ultrasound: Prospects as a tool to assess respiratory muscle involvement in amyotrophic lateral sclerosisRahul Reddy Rajula, Jitender Saini, Gopikrishnan Unnikrishnan, et al.Neurology. Clinical Practice|September 6, 2021
CASPR2-Related Morvan Syndrome: Autonomic, Polysomnographic, and Neuropsychological ObservationsPanda Sudha Swayang, Atchayaram Nalini, Veeramani Preethish-Kumar, et al.Journal of Neuromuscular Diseases|April 12, 2021
Comparison of The Carrier Frequency of Pathogenic Variants of DMD Gene in an Indian CohortDivya Nagabushana, Kiran Polavarapu, Mainak Bardhan, et al.Journal of Neuromuscular Diseases|October 11, 2021
Distinct and Recognisable Muscle MRI Pattern in a Series of Adults Harbouring an Identical GMPPB Gene MutationShahyan Siddiqui, Kiran Polavarapu, Mainak Bardhan, et al.Pageof 12