Showing results (1661-1670 of 3,402) with videos related to

Sort By:
Pageof 341
Neuromuscular Disorders : NMD|November 25, 2023
Magnetic resonance imaging-based criteria to differentiate dysferlinopathy from other genetic muscle diseasesCarla Bolano-Diaz, José Verdú-Díaz, Alejandro Gonzalez-Chamorro, et al.
Neuromuscular Disorders : NMD|February 15, 2024
Role of recovery of acetylcholine release in compromised neuromuscular junction functionJeppe Blichfeldt Winther, Jeanette Jeppesen Morgen, Martin Skov, et al.
Neuromuscular Disorders : NMD|February 14, 2024
"Amyopathic" MDA5-positive dermatomyositis with severe lung involvement presenting with net myositic morphological features - insights from an autopsy studyBenjamin Englert, Carsten Dittmayer, Hans-Hilmar Goebel, et al.
Neuromuscular Disorders : NMD|March 2, 2024
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN geneAlessia Perna, Luca Bosco, Fabiana Fattori, et al.
Neuromuscular Disorders : NMD|February 2, 2024
European Joint Programme on Rare Diseases workshop: LAMA2-muscular dystrophy: paving the road to therapy March 17-19, 2023, Barcelona, SpainHubert Smeets, Bram Verbrugge, Xavier Bulbena, et al.
Neuromuscular Disorders : NMD|February 4, 2024
Effect of nusinersen treatment on quality of life and motor function in adult patients with spinal muscular atrophyNazan Şimşek Erdem, Gökçe Yağmur Güneş Gencer, Abir Alaamel, et al.
Neuromuscular Disorders : NMD|May 22, 2024
Office-based respiratory assessment in patients with generalized myasthenia gravisMonica Alcantara, Carolina Barnett-Tapia, Vera Bril, et al.
Neuromuscular Disorders : NMD|May 21, 2024
Subclinical spinal muscular atrophy in a 60-year-old manSandra Palma, Pedro Pereira
Neuromuscular Disorders : NMD|May 28, 2024
Further expanding the phenotype of anti-Ku antibody associated disease in children and adolescentsEzgi Deniz Batu, Seher Şener, Göknur Haliloğlu, et al.
Neuromuscular Disorders : NMD|May 7, 2024
A rare complex structural variant of novel intragenic inversion combined with reciprocal translocation t(X;1)(p21.2;p13.3) in Duchenne muscular dystrophyYaye Wang, Xinmei Wen, Xin-Ming Shen, et al.
Pageof 341