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Neuromuscular Disorders : NMD|November 20, 2020
Tasks and interfaces in primary and specialized palliative care for Duchenne muscular dystrophy - A patients' perspectiveMaria Janisch, Kristin Boehme, Simone Thiele, et al.
Neuromuscular Disorders : NMD|November 21, 2020
Impact of a national population-based carrier-screening program on spinal muscular atrophy birthsSharon Aharoni, Yoram Nevo, Naama Orenstein, et al.
Neuromuscular Disorders : NMD|December 16, 2020
Whole-exome sequencing identifies a heterozygous mutation in SLC12A6 associated with hereditary sensory and motor neuropathyJiaying Shi, Fei Zhao, Xiaomin Pang, et al.
Neuromuscular Disorders : NMD|December 18, 2020
Dysphagia in adult myopathiesZohar Argov, Marianne de Visser
Neuromuscular Disorders : NMD|June 1, 2021
Hereditary transthyretin amyloidosis in multi-ethnic MalaysiansSoon-Chai Low, Nor Ashikin Md Sari, Cheng-Yin Tan, et al.
Neuromuscular Disorders : NMD|February 23, 2020
Inherited motor-sensory neuropathy with upper limb predominance associated with the tropomyosin-receptor kinase fused geneGian Maria Fabrizi, Helle Høyer, Federica Taioli, et al.
Neuromuscular Disorders : NMD|March 9, 2020
A hospital based epidemiological study of genetically determined muscle disease in south western NorwaySylvia Adele Husebye, Camilla Bratt Rebne, Ann-Elin Stokland, et al.
Neuromuscular Disorders : NMD|February 1, 2020
FHL1-related myopathy may not be classified by reducing bodies in muscle biopsyTing Chen, Xianghui Lu, Qiang Shi, et al.
Neuromuscular Disorders : NMD|February 1, 2020
Management of the dentoalveolar effects of tongue hypertrophy in patients with Duchenne muscular dystrophy: A pilot studyGregory S Antonarakis, Catherine Morel, Stavros Kiliaridis
Neuromuscular Disorders : NMD|February 2, 2020
Improving specialised care for neuromuscular patients reduces the frequency of preventable emergency hospital admissionsRenata S Scalco, Rosaline M Quinlivan, Laura Nastasi, et al.
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