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Neuromuscular Disorders : NMD|March 1, 1996
X-linked myotubular myopathy. 33rd ENMC International Workshop Soest. The Netherlands, 9-11 June 1995N Thomas, C Wallgren-Pettersson
Neuromuscular Disorders : NMD|March 31, 2010
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN)D M Cordelli, C Garone, V Marchiani, et al.
Neuromuscular Disorders : NMD|August 22, 2006
Induced dystrophin exon skipping in human muscle explantsG McClorey, A M Fall, H M Moulton, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Canine inflammatory myopathy associated with Leishmania Infantum infectionOrlando Paciello, Gaetano Oliva, Luigi Gradoni, et al.
Neuromuscular Disorders : NMD|December 17, 2008
A new phenotype of dysferlinopathy with congenital onsetC Paradas, L González-Quereda, N De Luna, et al.
Neuromuscular Disorders : NMD|December 17, 2008
A case of asymptomatic cytoplasmic body myopathy revealed by sinvastatinTeresinha Evangelista, José Ferro, Pedro Pereira, et al.
Neuromuscular Disorders : NMD|March 17, 2009
The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegiaEvangelia Sotiriou, Jorida Coku, Kurenai Tanji, et al.
Neuromuscular Disorders : NMD|January 27, 2009
Peripheral neuropathy and 46XY gonadal dysgenesis: a heterogeneous entityJonathan Baets, Ines Dierick, Chantal Ceuterick-de Groote, et al.
Neuromuscular Disorders : NMD|January 27, 2009
Dysphagia is present but mild in myotonic dystrophy type 2A A Tieleman, S Knuijt, J van Vliet, et al.
Neuromuscular Disorders : NMD|January 14, 2009
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutationEmmanuelle Uro-Coste, Marie-Christine Arné-Bes, Jean-François Pellissier, et al.
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