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Neuromuscular Disorders : NMD|June 24, 2014
Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutationsS Roos, U Lindgren, C Ehrstedt, et al.
Neuromuscular Disorders : NMD|July 29, 2020
Fatigue in patients with myasthenia gravis. A systematic review of the literatureAnnabel M Ruiter, Jan J G M Verschuuren, Martijn R Tannemaat
Neuromuscular Disorders : NMD|August 22, 2020
Early and long-term effect of the treatment with pyridostigmine in patients with GMPPB-related congenital myasthenic syndromeEdna Julieth Bobadilla-Quesada, Daniel Natera-de Benito, Laura Carrera-García, et al.
Neuromuscular Disorders : NMD|April 8, 2023
Detecting impaired muscle relaxation in myopathies with the use of motor cortical stimulationJoery P Molenaar, Esmee van Kleef, Elianne van Zandvoort, et al.
Neuromuscular Disorders : NMD|April 6, 2023
Collagen VI-related myopathies: clinical variability, phenotype-genotype correlation and exploratory transcriptome studyAnna Ky Kwong, Yanmin Zhang, Ronnie Sl Ho, et al.
Neuromuscular Disorders : NMD|April 6, 2023
Novel Alu-mediated deletions of the SMN1 gene were identified by ultra-long read sequencing technology in patients with spinal muscular atrophyJinli Bai, Yujin Qu, Shijia OuYang, et al.
Neuromuscular Disorders : NMD|September 11, 2007
Dysferlinopathy in the Jews of the Caucasus: a frequent mutation in the dysferlin geneE Leshinsky-Silver, Z Argov, L Rozenboim, et al.
Neuromuscular Disorders : NMD|September 11, 2007
Rhabdomyolysis in pontocerebellar hypoplasia type 2 (PCH-2)Peter G Barth, Monique M Ryan, Richard I Webster, et al.
Neuromuscular Disorders : NMD|June 27, 2008
Survival in SMA type I: a prospective analysis of 34 consecutive casesJ M Cobben, H H Lemmink, I Snoeck, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Constitutive upregulations of titin-based signalling proteins in KY deficient musclesJane Beatham, Katja Gehmlich, Peter F M van der Ven, et al.
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