Showing results (1421-1430 of 3,399) with videos related to

Sort By:
Pageof 340
Neuromuscular Disorders : NMD|March 1, 1996
An autosomal-recessive congenital myasthenic syndrome with tubular aggregates in a Libyan familyJ P Sieb, K Tolksdorf, R Dengler, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Optimized protein diagnosis in the autosomal recessive limb-girdle muscular dystrophiesL V Anderson
Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Impaired functional and structural recovery after muscle injury in dystrophic mdx miceA Irintchev, M Zweyer, A Wernig
Neuromuscular Disorders : NMD|January 1, 1997
Localization of laminin chains in the human retina: possible implications for congenital muscular dystrophy associated with alpha 2-chain of laminin deficiencyP Toti, C De Felice, A Malandrini, et al.
Neuromuscular Disorders : NMD|December 25, 2007
Differential diagnosis of muscular hypotonia in infants: the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VI)Uluç Yiş, Eray Dirik, Cèline Chambaz, et al.
Neuromuscular Disorders : NMD|November 7, 2016
A complex interplay of genetic and epigenetic events leads to abnormal expression of the DUX4 gene in facioscapulohumeral muscular dystrophyLaura Virginia Gatica, Alberto Luis Rosa
Neuromuscular Disorders : NMD|November 7, 2016
A new mutation in the mitochondrial tRNAPro gene associated with early-onset neuromuscular phenotype and ragged-red fibersGodelieve Morel, Sylvie Bannwarth, Annabelle Chaussenot, et al.
Neuromuscular Disorders : NMD|November 8, 2016
The gross motor function measure is valid for Fukuyama congenital muscular dystrophyTakatoshi Sato, Michiru Adachi, Kaho Nakamura, et al.
Neuromuscular Disorders : NMD|January 8, 2017
Is one trial enough for repeated testing? Same-day assessments of walking, mobility and fine hand use in people with myotonic dystrophy type 1Marie Kierkegaard, Emilie Petitclerc, Luc J Hébert, et al.
Pageof 340