본문 바로가기
KERD
논문KCI 등재

뚜렷한 소뇌위축 없이 실조증을 보이는 제8형 척수소뇌실조증 환자

Spinocerebellar Ataxia Type 8 Presenting as Ataxia without Definite Cerebellar Atrophy

2

조회

0

다운로드

0

인용

0

참고문헌

키워드

주제분류신경과학

참고문헌 (7)

  1. Koob MD, "An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)", Nat Genet, 21, pp.379~384 (1999)
  2. Day JW, "Spinocerebellar ataxia type 8: clinical features in a large family", Neurology, 55, pp.649~657 (2000)
  3. Juvonen V, "Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion", Ann Neurol, 48, pp.354~361 (2000)
  4. Ikeda Y, "Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan", Neurology, 54, pp.950~955 (2000)
  5. Ikeda Y, "Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes", Cerebellum, 7, pp.150~158 (2008)
  6. Factor SA, "False-positive SCA8 gene test in a patient with pathologically proven multiple system atrophy", Ann Neurol, 57, pp.462~463 (2005)
  7. Ikeda Y, "Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI", J Neurol Sci, 182, pp.76~79 (2000)

관련 논문AI추천

이 간행물의 다른 논문 (17건)