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http://hdl.handle.net/2445/126272
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DC Field | Value | Language |
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dc.contributor.author | Olivé i Plana, Montserrat | - |
dc.contributor.author | Odgerel, Zagaa | - |
dc.contributor.author | Martínez, Amaia | - |
dc.contributor.author | Poza, Juan José | - |
dc.contributor.author | García Bragado, Federico | - |
dc.contributor.author | Zabalza, Ramón J. | - |
dc.contributor.author | Jericó, Ivonne | - |
dc.contributor.author | González Mera, Laura | - |
dc.contributor.author | Shatunov, Alexey | - |
dc.contributor.author | Lee, Hee Suk | - |
dc.contributor.author | Armstrong i Morón, Judith | - |
dc.contributor.author | Maraví, Elías | - |
dc.contributor.author | Ramos Arroyo, María | - |
dc.contributor.author | Pascual Calvet, Jordi | - |
dc.contributor.author | Navarro, Carmen | - |
dc.contributor.author | Paradas, Carmen | - |
dc.contributor.author | Huerta Villanueva, Mariano | - |
dc.contributor.author | Márquez, Fabian | - |
dc.contributor.author | Gutierrez Rivas, Eduardo | - |
dc.contributor.author | Pou, Adolf | - |
dc.contributor.author | Ferrer, Isidro (Ferrer Abizanda) | - |
dc.contributor.author | Goldfarb, Lev G. | - |
dc.date.accessioned | 2018-11-21T09:07:36Z | - |
dc.date.available | 2018-11-21T09:07:36Z | - |
dc.date.issued | 2011-06-14 | - |
dc.identifier.issn | 0960-8966 | - |
dc.identifier.uri | http://hdl.handle.net/2445/126272 | - |
dc.description.abstract | Myofibrillar myopathies (MFM) are a group of disorders associated with mutations in DES, CRY A B, M YOT, ZASP, FLNC, or BAG3 genes and characterized by disintegration of myofibrils and accumulation of degradation products into intracellular inclusions. We retrospectively evaluated 53 M FM patients from 35 Spanish families. Studies included neurologic exam, muscle imaging, light and electron microscopic analysis of muscle biopsy, respiratory function testing and cardiologic work-up. Search for pathogenic mutations was accomplished by sequencing of coding regions of the six genes known to cause MFM. Mutations in M YOT were the predominant cause of MFM in Spain affecting 18 of 35 families, followed by DES in 11 and ZASP in 3; in 3 families the cause of MFM remains undetermined. Comparative analysis of DES, MYOT and ZASP associated phenotypes demonstrates substantial phenotypic distinctions that should be considered in studies of disease pathogenesis, for optimization of subtype-specific treatments and management, and directing molecular analysis. (C) 2011 Elsevier B.V. All rights reserved. | - |
dc.format.extent | 10 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Elsevier B.V. | - |
dc.relation.isformatof | Versió postprint del document publicat a: https://doi.org/10.1016/j.nmd.2011.05.002 | - |
dc.relation.ispartof | Neuromuscular Disorders, 2011, vol. 21, num. 8, p. 533-542 | - |
dc.relation.uri | https://doi.org/10.1016/j.nmd.2011.05.002 | - |
dc.rights | (c) Elsevier B.V., 2011 | - |
dc.source | Articles publicats en revistes (Patologia i Terapèutica Experimental) | - |
dc.subject.classification | Malalties musculars | - |
dc.subject.classification | Genètica | - |
dc.subject.classification | Malalties hereditàries | - |
dc.subject.classification | Espanya | - |
dc.subject.other | Muscular Diseases | - |
dc.subject.other | Genetics | - |
dc.subject.other | Genetic diseases | - |
dc.subject.other | Spain | - |
dc.title | Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/acceptedVersion | - |
dc.identifier.idgrec | 600948 | - |
dc.date.updated | 2018-11-21T09:07:36Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
dc.identifier.pmid | 21676617 | - |
Appears in Collections: | Articles publicats en revistes (Patologia i Terapèutica Experimental) Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) |
Files in This Item:
File | Description | Size | Format | |
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600948.pdf | 781.15 kB | Adobe PDF | View/Open |
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