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Two siblings with hiomocystinuria presenting with dystonia and parkinsonism

dc.contributor.authorVural, M
dc.contributor.authorApaydin, H
dc.contributor.authorOzekmekci, S
dc.contributor.authorEkinci, B
dc.date.accessioned2021-03-05T10:07:33Z
dc.date.available2021-03-05T10:07:33Z
dc.date.issued2004
dc.identifier.citationEkinci B., Apaydin H., Vural M., Ozekmekci S., "Two siblings with hiomocystinuria presenting with dystonia and parkinsonism", MOVEMENT DISORDERS, cilt.19, ss.962-964, 2004
dc.identifier.issn0885-3185
dc.identifier.otherav_a175ada6-9953-441b-9fb0-b41f64fbe366
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/108204
dc.identifier.urihttps://doi.org/10.1002/mds.20062
dc.description.abstractMovement disorders such as dystonia, chorea or tremor are rarely encountered in patients with homocystinuria. We present 2 siblings with laboratory-confirmed homocystinuria, one with severe generalized dystonia and the other with mild parkinsonism. The movement disorders in our patients appeared in the second and first decades, respectively. (C) 2004 Movement Disorder Society.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleTwo siblings with hiomocystinuria presenting with dystonia and parkinsonism
dc.typeMakale
dc.relation.journalMOVEMENT DISORDERS
dc.contributor.department, ,
dc.identifier.volume19
dc.identifier.issue8
dc.identifier.startpage962
dc.identifier.endpage964
dc.contributor.firstauthorID22007


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