Full metadata record
DC Field | Value | Language |
---|---|---|
dc.creator | Cabanyes-Truffin, J. (J.) | - |
dc.date.accessioned | 2012-06-05T17:53:26Z | - |
dc.date.available | 2012-06-05T17:53:26Z | - |
dc.date.issued | 2010 | - |
dc.identifier.citation | Cabanyes-Truffino J. Manifestaciones neurológicas en el adulto con premutación X frágil. Neurologia 2010 May;25(4):222-227. | es_ES |
dc.identifier.issn | 0213-4853 | - |
dc.identifier.uri | https://hdl.handle.net/10171/22478 | - |
dc.description.abstract | Introduction: 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.iso | spa | es_ES |
dc.publisher | Elsevier España | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.subject | Fragile X permutation | es_ES |
dc.subject | Tremor/ataxia syndrome | es_ES |
dc.subject | Cognitive deficit | es_ES |
dc.title | Manifestaciones neurológicas en el adulto con premutación X frágil | es_ES |
dc.title.alternative | Neurological signs in the adult with fragile-X premutation | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.type.driver | info:eu-repo/semantics/article | es_ES |
dc.identifier.doi | http://dx.doi.org/10.1016/j.nrl.2010.01.001 | es_ES |
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