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Neuromuscular Disorders : NMD|November 9, 2023
Respiratory function in a large cohort of treatment-naïve adult spinal muscular atrophy patients: a cross-sectional studyAlex Vicino, Luca Bello, Silvia Bonanno, et al.Neuromuscular Disorders : NMD|July 26, 2024
Improving Heckmatt muscle ultrasound grading scale through Rasch analysisJuerd Wijntjes, Christiaan Saris, Jonne Doorduin, et al.Neuromuscular Disorders : NMD|August 22, 2024
Niacin supplementation in a child with novel MTTN variant m.5670A>G causing early onset mitochondrial myopathy and NAD+ deficiencyJuho Aaltio, Liliya Euro, Olli Tynninen, et al.Neuromuscular Disorders : NMD|August 24, 2024
A cross-sectional study in 18 patients with typical and mild forms of nemaline myopathy in the NetherlandsEsmee S B van Kleef, Sanne A J H van de Camp, Jan T Groothuis, et al.Neuromuscular Disorders : NMD|June 1, 2024
Severe gastrointestinal problems in Duchenne muscular dystrophy: A case seriesA M Blokhuis, Kmaj Tytgat, J T Groothuis, et al.Neuromuscular Disorders : NMD|September 28, 2023
255th ENMC workshop: Muscle imaging in idiopathic inflammatory myopathies. 15th January, 16th January and 22nd January 2021 - virtual meeting and hybrid meeting on 9th and 19th September 2022 in Hoofddorp, The NetherlandsMarianne de Visser, Pierre Carlier, Jiří Vencovský, et al.Neuromuscular Disorders : NMD|September 16, 2023
Dysferlinopathy in Tunisia: clinical spectrum, genetic background and prognostic profileIkhlass Belhassen, Sirine Laroussi, Salma Sakka, et al.Neuromuscular Disorders : NMD|July 14, 2023
Exploring hand and upper limb function in patients with inclusion body myositis (IBM)Stephanie Hunn, Lindsay Alfano, Michelle Seiffert, et al.Neuromuscular Disorders : NMD|February 2, 2019
Evaluation and validation of sustained upgaze combined with the ice-pack test for ocular myasthenia gravis in AsiansHyun Joo Kee, Hee Kyung Yang, Jeong-Min Hwang, et al.Neuromuscular Disorders : NMD|February 6, 2019
6MWT performance correlates with peripheral neuropathy but not with cardiac involvement in patients with hereditary transthyretin amyloidosis (hATTR)Gian Luca Vita, Claudia Stancanelli, Luca Gentile, et al.Pageof 341