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 > MYOBASE > BIOLOGIE > biologie par discipline > biologie cellulaire > ultrastructure cellulaire > inclusion cellulaire > inclusion cytoplasmique > inclusion à corps cytoplasmiques
inclusion à corps cytoplasmiquesSynonyme(s)cytoplasmic inclusion body cytoplasmic inclusion bodies |
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New aspects of myofibrillar myopathies
Kley RA, Olivé M, Schröder R
Current opinion in neurology, 2016, 29, 5, p 628
Severe congenital actin related myopathy with myofibrillar myopathy features
Selcen D
Neuromuscular disorders : NMD, 2015, 25, 6, p 488
Skeletal muscle alpha-actin diseases (actinopathies) : pathology and mechanisms
Nowak KJ, Ravenscroft G, Laing NG
Acta neuropathologica, 2013, 125, 1, p. 19-32
Titin mutation segregates with hereditary myopathy with early respiratory failure
Pfeffer G, Elliott HR, Griffin H, et al.
Brain, 2012, 135, 6, p. 1695-1713
Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations
Mori-Yoshimura M, Monma K, Suzuki N, et al.
Journal of the neurological sciences, 2012, Epub 2012/11/07
A series of Chinese patients with desminopathy associated with 6 novel and 1 reported mutations in the desmin gene
Hong D, Wang Z, Zhang W, et al.
Neuropathology and applied neurobiology, 2011, 37, 3, p. 257-270
Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locus
Kottlors M, Moske-Eick O, Huebner A, et al.
Journal of the neurological sciences, 2010, 291, 1-2, p. 79-85
Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation
Knoblauch H, Geier C, Adams S, et al.
Annals of neurology, 2010, 67, 1, p. 136-140
Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited : identification of a second LIM domain mutation in FHL1
Schessl J, Columbus A, Hu Y, et al.
Neuropediatrics, 2010, 41, 1, p. 43-46
A case of asymptomatic cytoplasmic body myopathy revealed by sinvastatin
Evangelista T, Ferro J, Pereira P
Neuromuscular disorders : NMD, 2009, 19, 1, p. 66-68
Primary desminopathies
Schröder R, Vrabie A, Goebel HH
Journal of cellular and molecular medicine, 2007, 11, 3, p. 416-426
Delayed or late-onset type II glycogenosis with globular inclusions
Sharma MC, Schultze C, von Moers A, et al.
Acta neuropathologica, 2005, 110, 2, p. 151-157
Electron microscopy in neuromuscular disorders
Fernandez C, Figarella-Branger D, Meyronet D, et al.
Ultrastructural pathology, 2005, 29, p. 437-450
Mutations in dynein link motor neuron degeneration to defects in retrograde transport
Hafezparast M, Klocke R, Ruhrberg C, et al.
Science, 2003, 300, 5620, p. 808-812
Congenital cytoplasmic body myopathy with survival motor neuron (SMN) gene deletion or Werdnig-Hoffman disease ?
Vajsar J, Jay V, Ray P, et al.
Congrès : 2nd International congress of the World Muscle Society (16-18 Octobre 1997; Tunis)
Neuromuscular disorders : NMD, 1997, 7, 6-7, p. 430
Les filaments intermédiaires de desmine et autres protéines du cytosquelette dans une myopathie congénitale à inclusions et pathologies apparentées
Caron A
Thèse, 1996, 193 p
Amyloid filaments in inclusion body myosities. Novel findings provide insight into nature of filaments
Mendell JR, Sahenk Z, Gales T, et al.
Archives of neurology, 1991, 48, p. 1229-1234
