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dc.creatorCabanyes-Truffin, J. (J.)-
dc.date.accessioned2012-06-05T17:53:26Z-
dc.date.available2012-06-05T17:53:26Z-
dc.date.issued2010-
dc.identifier.citationCabanyes-Truffino J. Manifestaciones neurológicas en el adulto con premutación X frágil. Neurologia 2010 May;25(4):222-227.es_ES
dc.identifier.issn0213-4853-
dc.identifier.urihttps://hdl.handle.net/10171/22478-
dc.description.abstractIntroduction: Fragile X syndrome is an inherited form of mental retardation. It results from an abnormally expanded number of trinucleotide CGG repeats. Some grandfathers of these children become forgetful, have frequent falls and other neurological problems. Researchers have found a connection between fragile X syndrome and the neurological symptoms in elderly men. This resulted in the recognition of a syndrome originally referred to as ‘‘intention tremor, parkinsonism and generalised brain atrophy in carriers of a fragile X premutation’’. This premutation is also associated with premature ovarian failure.es_ES
dc.language.isospaes_ES
dc.publisherElsevier Españaes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectFragile X permutationes_ES
dc.subjectTremor/ataxia syndromees_ES
dc.subjectCognitive deficites_ES
dc.titleManifestaciones neurológicas en el adulto con premutación X frágiles_ES
dc.title.alternativeNeurological signs in the adult with fragile-X premutationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.type.driverinfo:eu-repo/semantics/articlees_ES
dc.identifier.doihttp://dx.doi.org/10.1016/j.nrl.2010.01.001es_ES

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