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Indian Journal of Endocrinology and Metabolism|November 20, 2013
Low dose liraglutide in Indian patients with type 2 diabetes in the real world settingDebmalya Sanyal, Anirban MajumdarJournal of Neuromuscular Diseases|May 6, 2026
Conflicts in Best Interest; Infants with severe neuromuscular disorders presenting to UK CourtsAnirban Majumdar, Silvia Sanchez MarcoPediatric Neurology|November 19, 2002
Delayed and severe but transient Tourette syndrome after head injuryAnirban Majumdar, Richard E AppletonNeuromuscular Disorders : NMD|November 7, 2016
Men with Duchenne muscular dystrophy and end of life planningDavid Abbott, Helen Prescott, Karen Forbes, et al.Journal of Neuromuscular Diseases|June 21, 2021
Inflammatory Myositis Secondary to Anti-Retroviral Therapy in a Child; Case Report and Review of the LiteratureMarie Monaghan, Charlotte Loh, Stephen Jones, et al.IEEE Transactions on Cybernetics|September 30, 2017
Static and Dynamic Synthesis of Bengali and Devanagari SignaturesMiguel A Ferrer, Sukalpa Chanda, Moises Diaz, et al.Case Reports in Pediatrics|September 17, 2025
Hypotonia, Ataxia, Developmental Delay and Tooth Enamel Defect Syndrome (HADDTS) due to a Heterozygous de Novo Missense Variant in CTBP1 Identified via Whole Genome SequencingSilvia Beatriz Sanchez Marco, Emily Pardington, Marie Monaghan, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 11, 2008
Syndrome of fixed dystonia in adolescents--short term outcome in 4 casesAnirban Majumdar, Jesús López-Casas, Pilar Poo, et al.Neuromuscular Disorders : NMD|February 2, 2020
A novel de novo ACTA1 variant in a patient with nemaline myopathy and mitochondrial Complex I deficiencyShpresa Pula, Kathryn Urankar, Andrew Norman, et al.Journal of Neuromuscular Diseases|January 28, 2020
Clinical and Genetic Features in a Series of Eight Unrelated Patients with Neuropathy Due to Glycyl-tRNA Synthetase (GARS) VariantsNatalie Forrester, Rohini Rattihalli, Rita Horvath, et al.Pageof 4