Showing results (101-110 of 117) with videos related to
Sort By:
Pageof 12
Neuromuscular Disorders : NMD|April 9, 2008
Late onset in dysferlinopathy widens the clinical spectrumL Klinge, A F Dean, W Kress, et al.Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.The Journal of Biological Chemistry|May 23, 1997
A role of dystroglycan in schwannoma cell adhesion to lamininK Matsumura, A Chiba, H Yamada, et al.Journal of Neurochemistry|April 1, 1996
Characterization of dp6troglycan-laminin interaction in peripheral nerveH Yamada, A Chiba, T Endo, et al.Neuromuscular Disorders : NMD|February 13, 2001
Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophiesR Pogue, L V Anderson, A Pyle, et al.Journal of Molecular Neuroscience : MN|October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophiesM Vainzof, L V Anderson, E M McNally, et al.Neuropathology and Applied Neurobiology|February 8, 2012
Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insightsU Rüb, K Bürk, D Timmann, et al.Human Molecular Genetics|April 10, 1999
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)T Weiler, R Bashir, L V Anderson, et al.European Journal of Human Genetics : EJHG|October 20, 2000
Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD familyI B Ginjaar, A L Kneppers, J D v d Meulen, et al.Brain : a Journal of Neurology|October 6, 1997
Utrophin abundance is reduced at neuromuscular junctions of patients with both inherited and acquired acetylcholine receptor deficienciesC R Slater, C Young, S J Wood, et al.Pageof 12