Showing results (1971-1980 of 3,403) with videos related to
Sort By:
Pageof 341
Neuromuscular Disorders : NMD|May 1, 1996
Mitochondrial abnormalities in oculopharyngeal muscular dystrophyK T Wong, D Dick, J R AndersonNeuromuscular Disorders : NMD|May 1, 1996
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiencyM Villanova, A Malandrini, R Biancotti, et al.Neuromuscular Disorders : NMD|March 1, 1993
Accumulating autofluorescent material as a marker for early changes in the spinal cord of the Mnd mouseA Messer, J PlummerNeuromuscular Disorders : NMD|March 1, 1993
Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weaknessC A Sewry, A Sansome, A Clerk, et al.Neuromuscular Disorders : NMD|November 7, 2016
Men with Duchenne muscular dystrophy and end of life planningDavid Abbott, Helen Prescott, Karen Forbes, et al.Neuromuscular Disorders : NMD|November 7, 2016
Widening the spectrum of filamin-C myopathy: Predominantly proximal myopathy due to the p.A193T mutation in the actin-binding domain of FLNCFleur J A van den Bogaart, Kristl G Claeys, Rudolf A Kley, et al.Neuromuscular Disorders : NMD|November 7, 2016
Ischemic stroke due to hypoperfusion in a patient with a previously unrecognized Danon diseaseMarco Marino, Olimpia Musumeci, Giuseppe Paleologo, et al.Neuromuscular Disorders : NMD|November 8, 2016
Use of the six-minute walk test to characterize golden retriever muscular dystrophyAustin R Acosta, Emiko Van Wie, William B Stoughton, et al.Neuromuscular Disorders : NMD|November 24, 2016
Tubular aggregate myopathy with features of Stormorken disease due to a new STIM1 mutationJean-Baptiste Noury, Johann Böhm, Georges Arielle Peche, et al.Neuromuscular Disorders : NMD|December 3, 2016
Confirmation of the GNB4 gene as causal for Charcot-Marie-Tooth disease by a novel de novo mutation in a Czech patientPetra Laššuthová, Dana Šafka Brožková, Jana Neupauerová, et al.Pageof 341