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Neuromuscular Disorders : NMD|July 10, 1999
A novel de novo mutation in the triple helix of the COL6A3 gene in a two-generation Italian family affected by Bethlem myopathy. A diagnostic approach in the mutations' screening of type VI collagenG Pepe, E Bertini, B Giusti, et al.Neuromuscular Disorders : NMD|March 29, 2000
Lipopolysaccharides of a Campylobacter coli isolate from a patient with Guillain-Barré syndrome display ganglioside mimicryM Bersudsky, P Rosenberg, B Rudensky, et al.Neuromuscular Disorders : NMD|March 27, 1999
Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX miceR Krämer, H Lochmüller, A Abicht, et al.Neuromuscular Disorders : NMD|October 29, 2000
Unusual expression of emerin in a patient with X-linked Emery-Dreifuss muscular dystrophyC Di Blasi, L Morandi, M Raffaele di Barletta, et al.Neuromuscular Disorders : NMD|October 29, 2000
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophyB Kerst, D Mennerich, M Schuelke, et al.Neuromuscular Disorders : NMD|February 13, 2001
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3C Barhoumi, R Amouri, C Ben Hamida, et al.Neuromuscular Disorders : NMD|February 13, 2001
Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrieversN J Olby, N J Sharp, L V Anderson, et al.Neuromuscular Disorders : NMD|February 13, 2001
Mast cell proliferation and alterations in bFGF amount and localization are involved in the response of muscle to dystrophin deficiency in hypertrophic feline dystrophyG Seiler, M Welle, A Busato, et al.Neuromuscular Disorders : NMD|October 17, 2017
Different profiles of upper limb function in four types of neuromuscular disordersArjen Bergsma, Mariska M H P Janssen, Alexander C H Geurts, et al.Neuromuscular Disorders : NMD|October 15, 2017
Reduced renal function in patients with Myotonic Dystrophy type 1 and the association to CTG expansion and other potential risk factors for chronic kidney diseaseAnnika Aldenbratt, Christopher Lindberg, Maria K SvenssonPageof 340