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Neuromuscular Disorders : NMD|July 19, 2011
Deficiency of the mitochondrial phosphate carrier presenting as myopathy and cardiomyopathy in a family with three affected childrenJohannes A Mayr, Franz A Zimmermann, Rita Horváth, et al.
Neuromuscular Disorders : NMD|July 12, 2011
Hereditary peripheral neuropathies of childhood: an overview for cliniciansJo M Wilmshurst, Robert Ouvrier
Neuromuscular Disorders : NMD|July 12, 2011
Two cases of oculopharyngeal muscular dystrophy (OPMD) with the rare PABPN1 c.35G>C; p.Gly12Ala point mutationDavid O Robinson, David Hilton-Jones, David Mansfield, et al.
Neuromuscular Disorders : NMD|April 13, 2011
Limb edema and anasarca associated with severe dermatomyositis: report of four casesYaohui Chai, Tulio E Bertorini, Yingjun D Li, et al.
Neuromuscular Disorders : NMD|May 3, 2011
Characterizing the phenotypic manifestations of MFN2 R104W mutation in Charcot-Marie-Tooth type 2Adriana Borges Genari, Vinícius Horácio Stefani Borghetti, Silmara Paula Gouvêa, et al.
Neuromuscular Disorders : NMD|March 29, 2011
Reduction of acethylcolinesterase activity in the brain of mdx miceClarissa M Comim, Thais Moraz, Igor Abreu, et al.
Neuromuscular Disorders : NMD|November 16, 2011
Three cases of myasthenia gravis from one family with variations in clinical features and serum antibodiesYuping Chen, Wei Wang, Dongning Wei, et al.
Neuromuscular Disorders : NMD|December 3, 2011
Quantitative muscle ultrasound is a promising longitudinal follow-up tool in Duchenne muscular dystrophyMerel Jansen, Nens van Alfen, Maria W G Nijhuis van der Sanden, et al.
Neuromuscular Disorders : NMD|December 3, 2011
Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII)Olimpia Musumeci, Claudio Bruno, Tiziana Mongini, et al.
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