Neurological manifestations in two related xeroderma pigmentosum group D patients: complications of the late-onset type of the juvenile form.
Identifieur interne : 004D61 ( Ncbi/Curation ); précédent : 004D60; suivant : 004D62Neurological manifestations in two related xeroderma pigmentosum group D patients: complications of the late-onset type of the juvenile form.
Auteurs : T. Stojkovic [France] ; L. Defebvre ; X. Quilliet ; E. Eveno ; A. Sarasin ; M. Mezzina ; A. DestéeSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1997.
English descriptors
- KwdEn :
- Adult, Age of Onset, Atrophy, Cerebellar Ataxia (diagnosis), Cerebellar Ataxia (genetics), Cerebellar Ataxia (physiopathology), Cerebellum (pathology), Child, Disease Progression, Female, Humans, Magnetic Resonance Imaging, Movement Disorders (diagnosis), Movement Disorders (genetics), Movement Disorders (physiopathology), Nerve Degeneration (genetics), Xeroderma Pigmentosum (complications), Xeroderma Pigmentosum (genetics), Xeroderma Pigmentosum (physiopathology).
- MESH :
- complications : Xeroderma Pigmentosum.
- diagnosis : Cerebellar Ataxia, Movement Disorders.
- genetics : Cerebellar Ataxia, Movement Disorders, Nerve Degeneration, Xeroderma Pigmentosum.
- pathology : Cerebellum.
- physiopathology : Cerebellar Ataxia, Movement Disorders, Xeroderma Pigmentosum.
- Adult, Age of Onset, Atrophy, Child, Disease Progression, Female, Humans, Magnetic Resonance Imaging.
DOI: 10.1002/mds.870120428
PubMed: 9251090
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pubmed:9251090Le document en format XML
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