208 related articles for article (PubMed ID: 8615077)
1. Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype.
Robitaille Y; Schut L; Kish SJ
Acta Neuropathol; 1995; 90(6):572-81. PubMed ID: 8615077
[TBL] [Abstract][Full Text] [Related]
2. [Neuropathological study of autosomal dominant ataxia linked to loci on chromosome 6p (SCA 1)].
Hamada K; Fukazawa T; Yanagihara T; Hamada T; Yoshida K; Sasaki H; Tashiro K
No To Shinkei; 1993 Nov; 45(11):1045-9. PubMed ID: 8297664
[TBL] [Abstract][Full Text] [Related]
3. [A family with Menzel's disease showing dementia and various extrapyramidal symptoms].
Iwabuchi K; Nagatomo H; Tanabe T; Oda T; Itoh H; Hanihara T; Yagishita S
No To Shinkei; 1993 Sep; 45(9):841-9. PubMed ID: 8217410
[TBL] [Abstract][Full Text] [Related]
4. Synapses in the hereditary ataxias.
Koeppen AH; Dickson AC; Lamarche JB; Robitaille Y
J Neuropathol Exp Neurol; 1999 Jul; 58(7):748-64. PubMed ID: 10411345
[TBL] [Abstract][Full Text] [Related]
5. Brain acetylcholinesterase activity is markedly reduced in dominantly-inherited olivopontocerebellar atrophy.
Kish SJ; Schut L; Simmons J; Gilbert J; Chang LJ; Rebbetoy M
J Neurol Neurosurg Psychiatry; 1988 Apr; 51(4):544-8. PubMed ID: 3164041
[TBL] [Abstract][Full Text] [Related]
6. Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locus.
Subramony SH; Fratkin JD; Manyam BV; Currier RD
Mov Disord; 1996 Mar; 11(2):174-80. PubMed ID: 8684388
[TBL] [Abstract][Full Text] [Related]
7. Multiple system atrophy with retinal degeneration in a young child.
Nishimura M; Mito T; Takashima S; Kawahara H; Tanaka J; Nakamura H; Kisa T
Neuropediatrics; 1987 May; 18(2):91-5. PubMed ID: 3474543
[TBL] [Abstract][Full Text] [Related]
8. Olivopontocerebellar atrophy: immunocytochemical and Golgi observations.
Koeppen AH; Mitzen EJ; Hans MB; Barron KD
Neurology; 1986 Nov; 36(11):1478-88. PubMed ID: 3463885
[TBL] [Abstract][Full Text] [Related]
9. Olivopontocerebellar atrophy in a large Iakut kinship in eastern Siberia.
Goldfarb LG; Chumakov MP; Petrov PA; Fedorova NI; Gajdusek DC
Neurology; 1989 Nov; 39(11):1527-30. PubMed ID: 2812335
[TBL] [Abstract][Full Text] [Related]
10. A case of spinocerebellar ataxia type 6 mimicking olivopontocerebellar atrophy.
Nakagawa N; Katayama T; Makita Y; Kuroda K; Aizawa H; Kikuchi K
Neuroradiology; 1999 Jul; 41(7):501-3. PubMed ID: 10450843
[TBL] [Abstract][Full Text] [Related]
11. Clinicopathology of spinocerebellar degeneration: its correlation to the unstable CAG repeat of the affected gene.
Yagishita S; Inoue M
Pathol Int; 1997 Jan; 47(1):1-15. PubMed ID: 9051687
[TBL] [Abstract][Full Text] [Related]
12. Machado-Joseph disease: an autosomal dominant motor system degeneration.
Rosenberg RN
Mov Disord; 1992; 7(3):193-203. PubMed ID: 1620135
[TBL] [Abstract][Full Text] [Related]
13. The hereditary ataxias.
Koeppen AH
J Neuropathol Exp Neurol; 1998 Jun; 57(6):531-43. PubMed ID: 9630233
[TBL] [Abstract][Full Text] [Related]
14. Hereditary ataxia.
Rosenberg RN; Grossman A
Neurol Clin; 1989 Feb; 7(1):25-36. PubMed ID: 2564162
[TBL] [Abstract][Full Text] [Related]
15. Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family?
Eto K; Sumi SM; Bird TD; McEvoy-Bush T; Boehnke M; Schellenberg G
Arch Neurol; 1990 Sep; 47(9):968-74. PubMed ID: 2396938
[TBL] [Abstract][Full Text] [Related]
16. [Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)].
Iwabuchi K; Kosaka K; Haga C; Tuchiya K; Amano N; Itoh K; Yagishita S; Mizutani Y
No To Shinkei; 1991 Jun; 43(6):561-8. PubMed ID: 1654964
[TBL] [Abstract][Full Text] [Related]
17. Electroencephalographic findings of hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
Inazuki G; Baba K; Naito H
Jpn J Psychiatry Neurol; 1989 Jun; 43(2):213-20. PubMed ID: 2529387
[TBL] [Abstract][Full Text] [Related]
18. [Peculiar forms of familial olivo-ponto-cerebellar atrophy (Menzel type) and Joseph disease; clinico-neuropathological study of two families with nosological considerations].
Ikeda T
Seishin Shinkeigaku Zasshi; 1987; 89(4):245-81. PubMed ID: 3476971
[No Abstract] [Full Text] [Related]
19. [Linkage study of Machado-Joseph disease: genetic evidence for the locus different from SCA1].
Sasaki H; Wakisaka A; Tashiro K; Hamada T; Katoh T
Rinsho Shinkeigaku; 1992 Jan; 32(1):13-6. PubMed ID: 1628431
[TBL] [Abstract][Full Text] [Related]
20. Infantile-onset spinocerebellar ataxia: MR and CT findings.
Koskinen T; Valanne L; Ketonen LM; Pihko H
AJNR Am J Neuroradiol; 1995 Aug; 16(7):1427-33. PubMed ID: 7484627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
