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dc.contributor.authorErtan, Fatos Sibel
dc.contributor.authorElmali, Ayşe Deniz
dc.contributor.authorBaslar, Zafer
dc.contributor.authorGunduz, Aysegul
dc.date.accessioned2021-03-04T08:10:09Z
dc.date.available2021-03-04T08:10:09Z
dc.date.issued2015
dc.identifier.citationElmali A. D. , Gunduz A., Baslar Z., Ertan F. S. , "Considering Huntington's Disease and Neuroacanthocytosis in the Differential Diagnosis of Senile Chorea", TURKISH JOURNAL OF NEUROLOGY, cilt.21, sa.3, ss.119-123, 2015
dc.identifier.othervv_1032021
dc.identifier.otherav_61eca10b-1a03-483c-8127-45746c7c5331
dc.identifier.urihttp://hdl.handle.net/20.500.12627/68218
dc.identifier.urihttps://doi.org/10.4274/tnd.34545
dc.description.abstractSporadic chorea that presents after the age of 50 years is called "senile chorea". Senile chorea is a rare entity with a wide differential diagnosis list. Causes of senile chorea include vascular and metabolic diseases, adverse events related to medications, hematologic and immune system diseases, genetic and sporadic neurodegenerative syndromes, and paraneoplastic disorders. Although the most common etiologies are vascular and metabolic disorders, neuroacanthocytosis, Wilson's and Huntington's disease are included in the differential diagnosis.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleConsidering Huntington's Disease and Neuroacanthocytosis in the Differential Diagnosis of Senile Chorea
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF NEUROLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume21
dc.identifier.issue3
dc.identifier.startpage119
dc.identifier.endpage123
dc.contributor.firstauthorID95431


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