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Neuromuscular Disorders : NMD|September 1, 1994
Calcitonin gene-related peptide-like immunoreactivity, in botulinum toxin-paralysed rat musclesS M Hassan, F G Jennekens, G Wieneke, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Bethlem myopathy: early-onset benign autosomal dominant myopathy with contractures. Description of two new familiesL Merlini, L Morandi, C Granata, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Neonatal nemaline myopathy with abundant intranuclear rodsR J Barohn, C E Jackson, K S Kagan-Hallet
Neuromuscular Disorders : NMD|June 1, 1997
Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?B Udd, R Krahe, C Wallgren-Pettersson, et al.
Neuromuscular Disorders : NMD|May 1, 1997
External ophthalmoplegia in neuromuscular disorders: case report and review of the literatureK J Jones, K N North
Neuromuscular Disorders : NMD|May 1, 1997
Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosisP Guicheney, N Vignier, A Helbling-Leclerc, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matterB Echenne, F Rivier, A J Jellali, et al.
Neuromuscular Disorders : NMD|October 31, 2009
Coinheritance of Noonan syndrome and Becker muscular dystrophyArgirios Dinopoulos, Anna Papadopoulou, Panagiota Manta, et al.
Neuromuscular Disorders : NMD|November 18, 2005
Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathyR Horváth, B G H Schoser, J Müller-Höcker, et al.
Neuromuscular Disorders : NMD|July 15, 2025
Potential relationship between MuSK-MG and autologous hematopoietic stem cell transplantation: a case reportRyo Sasaki, Ryoma Nakamura, Yoshiaki Takahashi, et al.
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