Showing results (2531-2540 of 3,410) with videos related to

Sort By:
Pageof 341
Neuromuscular Disorders : NMD|February 6, 2026
Spontaneous remission in statin-associated HMGCR-positive immune-mediated necrotizing myopathy after statin withdrawalAgata A Mossakowski, Daniel Pascale, Yves Allenbach, et al.
Neuromuscular Disorders : NMD|February 4, 2026
Refining functional phenotypes in an international cohort of untreated paediatric type 2 and 3 SMA patients using the Revised Hammersmith ScaleE Milev, G Stimpson, D Ramsey, et al.
Neuromuscular Disorders : NMD|February 4, 2026
Urinary glucose tetrasaccharide tracks disease activity in late-onset Pompe diseaseCristina Domínguez-González, Domenico Iannucci, James Clark, et al.
Neuromuscular Disorders : NMD|June 12, 2025
Prevalence and prognostic impact of cardiac resonance abnormalities in myotonic dystrophy patientsVincenzo Russo, Alfredo Mauriello, Roberta Bottino, et al.
Neuromuscular Disorders : NMD|June 24, 2025
Multi-omics approach identifies a novel recessive pathogenic variant in the TNNT3 gene in two siblings with congenital myopathyJuliane S Müller, Shira Rabinowicz, Irina Zaharieva, et al.
Neuromuscular Disorders : NMD|June 20, 2025
An HTLV-1 carrier with sporadic late-onset nemaline myopathy accompanied by skin lesions indicating indolent adult T-cell leukemia/lymphoma and Sjögren's syndrome: a case report and literature reviewAko Miyata, Tomomi Shijo, Rumiko Izumi, et al.
Neuromuscular Disorders : NMD|March 29, 2025
Identifying novel AGRN variants in congenital myasthenic syndrome: insights from three Iranian familiesHadi Gharebaghian, Aida Ghasemi, Omid Hesami, et al.
Neuromuscular Disorders : NMD|May 1, 2025
Sporadic late onset nemaline myopathy responsive to plasma exchanges discovered during a Graft-versus-host diseaseSarah Souvannanorath, Giovanni Umberto Borin, Rabah Redjoul, et al.
Neuromuscular Disorders : NMD|June 14, 2023
Novel p.Asp27Glu ACTA1 variant features congenital myopathy with finger flexor weakness, cardiomyopathy, and cardiac conduction defectsBridget Mulvany-Robbins, Brendan Putko, Laura Schmitt, et al.
Neuromuscular Disorders : NMD|March 4, 2026
Overview of facioscapulohumeral dystrophy clinical features and diagnostic pathwayBrianna N Brun, Neil Camarta, Nick Johnson, et al.
Pageof 341