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histopathologie musculaireSynonyme(s)altération musculaire ;histological muscle lesion ;lésion histologique musculaire ;lésion microscopique musculaire ;microlésion musculaire ;microscopic muscle lesion ;muscle micro-injury muscle histopathologyVoir aussi |
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Salih Myopathy : Synonym: Early-Onset Myopathy with Fatal Cardiomyopathy
Hackman P, Savarese M, Carmignac V, et al.
GeneReviews® [Internet], 2019
Myosites nécrosantes auto-immunes : vers une révision des critères diagnostiques histologiques
Urtizberea JA, Cukierman L
2018
Congenital titinopathy: Comprehensive characterisation and pathogenic insights
Oates EC, Jones KJ, Donkervoort S, et al.
Annals of neurology, 2018
Characterization of congenital myopathies at a Korean neuromuscular center
Park YE, Shin JH, Kim HS, et al.
Muscle & Nerve, 2018
Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement
Dabaj I, Carlier RY, Gómez-Andrés D, et al.
Muscle & Nerve, 2018
The first French case of MATR3-related distal myopathy: Clinical, radiological and histopathological characterization
Barp A, Malfatti E, Metay C, et al.
Revue neurologique, 2018
Pompe disease: An Indian series diagnosed on muscle biopsy by ultrastructural characterization
Kakkar A, Sharma MC, Nambirajan A, et al.
Ultrastructural pathology, 2018
Clinical and molecular consequences of exon 78 deletion in DMD gene
Traverso M, Assereto S, Baratto S, et al.
Journal of human genetics, 2018
Immune-Mediated Necrotizing Myopathy and Dietary Sources of Statins
Barbacki A, Fallavollita SA, Karamchandani J, et al.
Annals of internal medicine, 2018
Genetic and clinical findings in a Chinese cohort of patients with collagen VI-related myopathies
Fan Y, Liu A, Wei C, et al.
Clinical genetics, 2018
Whole exome sequencing discloses a pathogenic MTM1 gene mutation and ends the diagnostic odyssey in an older woman with a progressive and seemingly sporadic myopathy: Case report and literature review of MTM1 manifesting female carriers
Felice KJ, Whitaker CH, Wu Q
Neuromuscular disorders : NMD, 2018
Dystrophinopathy muscle biopsies in the genetic testing ERA: One center's data
Carlson CR, Moore SA, Mathews KD
Muscle & Nerve, 2018
Inclusion body myositis and human immunodeficiency virus type 1: A new case report and literature review
Couture P, Malfatti E, Morau G, et al.
Neuromuscular disorders : NMD, 2018, 28, 4, p 334
CASQ1 mutations impair calsequestrin polymerization and cause tubular aggregate myopathy
Böhm J, Lornage X, Chevessier F, et al.
Acta neuropathologica, 2018, 135, 1, p 149
Riboflavin transporter deficiency mimicking mitochondrial myopathy caused by complex II deficiency
Nimmo GAM, Ejaz R, Cordeiro D, et al.
American Journal of Medical Genetics Part A, 2018, 176, 2, p 399
Distal myopathy due to BICD2 mutations
Souza PVS, Pinto WBVR, Aivazoglou LU, et al.
Clinical neurology and neurosurgery, 2018, 165, p 47
Immune-Mediated Necrotizing Myopathy
Pinal-Fernández I, Casal-Dominguez M, Mammen AL
Current rheumatology reports, 2018, 20, 4
New Myositis Classification Criteria-What We Have Learned Since Bohan and Peter
Leclair V, Lundberg IE
Current rheumatology reports, 2018, 20, 4
Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodies
Nilipour Y, Nafissi S, Tjust AE, et al.
European journal of neurology, 2018, 25, 6, p 841
Ryanodine channel complex stabilizer compound S48168/ARM210 as a disease modifier in dystrophin-deficient mdx mice: proof-of-concept study and independent validation of efficacy
Capogrosso RF, Mantuano P, Uaesoontrachoon K, et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2018, 32, 2, p 1025
Increasing Agrin Function Antagonizes Muscle Atrophy and Motor Impairment in Spinal Muscular Atrophy
Boido M, De Amicis E, Valsecchi V, et al.
Frontiers in cellular neuroscience, 2018, 12
Novel Variants in Individuals with RYR1-Related Congenital Myopathies: Genetic, Laboratory, and Clinical Findings
Todd JJ, Razaqyar MS, Witherspoon JW, et al.
Frontiers in neurology, 2018, 9
The genetics of congenital myopathies
Gonorazky HD, Bonnemann CG, Dowling JJ
Handbook of clinical neurology, 2018, 148, p 549
Dual AAV gene therapy for Duchenne muscular dystrophy with a 7-kb mini-dystrophin gene in the canine model
Kodippili K, Hakim C, Pan X, et al.
Human gene therapy, 2018, 29, 3, p 299
