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Gopikrishnan

Showing results (191-200 of 200) with videos related to

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Neurology India|December 18, 2024
Clinical Manifestations of Anti-GABA-B Receptor Encephalitis: A Case SeriesJeeva P Jiju, Sneha Santhosh, Chirag S Lalwani, et al.
Multiple Sclerosis and Related Disorders|December 30, 2024
MOG IgG antibody positivity from laboratory to clinical practice: A real world experienceTejas Shivarthi, Mahima Sriram, Muddana Nikhilesh, et al.
Neurogenetics|August 5, 2024
Phenotype-genotype spectrum of a cohort of congenital muscular dystrophies: a single-centre experience from IndiaTanushree Chawla, Saraswati Nashi, Dipti Baskar, et al.
Global Medical Genetics|February 16, 2022
Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from IndiaValakunja H Ganaraja, Kiran Polavarapu, Mainak Bardhan, et al.
Neuromuscular Disorders : NMD|April 26, 2024
Partial loss of desmin expression due to a leaky splice site variant in the human DES gene is associated with neuromuscular transmission defectsKiran Polavarapu, Daniel O'Neil, Rachel Thompson, et al.
Neuromuscular Disorders : NMD|January 5, 2025
Magnetic resonance imaging in idiopathic inflammatory myopathies: deciphering the pattern of muscle involvementS Sridhar, Saraswati Nashi, Karthik Kulanthaivelu, et al.
Journal of Neuromuscular Diseases|August 30, 2024
GNE Myopathy: Genotype - Phenotype Correlation and Disease Progression in an Indian CohortDipti Baskar, Nishanth Reddy, Veeramani Preethish-Kumar, et al.
Brain : a Journal of Neurology|September 18, 2023
Clinical and genetic characterisation of a large Indian congenital myasthenic syndrome cohortKiran Polavarapu, Balaraju Sunitha, Ana Töpf, et al.
World Neurosurgery|November 25, 2023
Monomelic Amyotrophy/Hirayama Disease: Surgical Outcome in a Large Cohort of Indian PatientsSeena Vengalil, Nupur Pruthi, Dhananjay Bhat, et al.
Brain : a Journal of Neurology|September 28, 2023
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathiesAnnette Lischka, Katja Eggermann, Christopher J Record, et al.
Pageof 20

Showing results (191-200 of 200) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 200 results.
Neurology India|December 18, 2024
Clinical Manifestations of Anti-GABA-B Receptor Encephalitis: A Case SeriesJeeva P Jiju, Sneha Santhosh, Chirag S Lalwani, et al.
Multiple Sclerosis and Related Disorders|December 30, 2024
MOG IgG antibody positivity from laboratory to clinical practice: A real world experienceTejas Shivarthi, Mahima Sriram, Muddana Nikhilesh, et al.
Neurogenetics|August 5, 2024
Phenotype-genotype spectrum of a cohort of congenital muscular dystrophies: a single-centre experience from IndiaTanushree Chawla, Saraswati Nashi, Dipti Baskar, et al.
Global Medical Genetics|February 16, 2022
Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from IndiaValakunja H Ganaraja, Kiran Polavarapu, Mainak Bardhan, et al.
Neuromuscular Disorders : NMD|April 26, 2024
Partial loss of desmin expression due to a leaky splice site variant in the human DES gene is associated with neuromuscular transmission defectsKiran Polavarapu, Daniel O'Neil, Rachel Thompson, et al.
Neuromuscular Disorders : NMD|January 5, 2025
Magnetic resonance imaging in idiopathic inflammatory myopathies: deciphering the pattern of muscle involvementS Sridhar, Saraswati Nashi, Karthik Kulanthaivelu, et al.
Journal of Neuromuscular Diseases|August 30, 2024
GNE Myopathy: Genotype - Phenotype Correlation and Disease Progression in an Indian CohortDipti Baskar, Nishanth Reddy, Veeramani Preethish-Kumar, et al.
Brain : a Journal of Neurology|September 18, 2023
Clinical and genetic characterisation of a large Indian congenital myasthenic syndrome cohortKiran Polavarapu, Balaraju Sunitha, Ana Töpf, et al.
World Neurosurgery|November 25, 2023
Monomelic Amyotrophy/Hirayama Disease: Surgical Outcome in a Large Cohort of Indian PatientsSeena Vengalil, Nupur Pruthi, Dhananjay Bhat, et al.
Brain : a Journal of Neurology|September 28, 2023
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathiesAnnette Lischka, Katja Eggermann, Christopher J Record, et al.
Pageof 20