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Neuromuscular Disorders : NMD|April 17, 2007
GDAP1 mutations in Czech families with early-onset CMTL Baránková, E Vyhnálková, S Züchner, et al.Neuromuscular Disorders : NMD|November 2, 1999
Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndromeB Moghadaszadeh, H Topaloglu, L Merlini, et al.Differentiation; Research in Biological Diversity|March 29, 2001
Emerin expression at the early stages of myogenic differentiationG Lattanzi, A Ognibene, P Sabatelli, et al.Human Molecular Genetics|October 1, 1995
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the diseaseS Bione, K Small, V M Aksmanovic, et al.Neurology|December 2, 2009
Autosomal recessive Bethlem myopathyF Gualandi, A Urciuolo, E Martoni, et al.Journal of Medical Genetics|March 4, 2005
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophyV Cenni, P Sabatelli, E Mattioli, et al.Journal of Cellular Physiology|September 29, 2011
Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathiesP Sabatelli, E Palma, A Angelin, et al.Acta Neuropathologica|August 31, 2000
Emerin presence in plateletsS Squarzoni, P Sabatelli, C Capanni, et al.Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.Human Mutation|July 5, 2001
Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian familiesM L Mostacciuolo, E Righetti, M Zortea, et al.Pageof 18