143 related articles for article (PubMed ID: 3251076)
1. Linkage study of dominantly inherited olivo-ponto-cerebellar atrophy (OPCA) and Holmes' ataxia.
Sasaki H; Wakisaka A; Katoh T; Yoshida MC; Hamada T; Shima K; Matsuura T; Tashiro K
Jinrui Idengaku Zasshi; 1988 Dec; 33(4):423-38. PubMed ID: 3251076
[No Abstract] [Full Text] [Related]
2. [A clinical study of a family affected with HLA-linked hereditary spinocerebellar ataxia].
Sasaki H; Hamada T; Wakisaka A; Tashiro K
No To Shinkei; 1990 Nov; 42(11):1103-11. PubMed ID: 2076357
[TBL] [Abstract][Full Text] [Related]
3. CT in autosomal dominant and idiopathic cerebellar ataxia.
Wittkämper A; Wessel K; Brückmann H
Neuroradiology; 1993; 35(7):520-4. PubMed ID: 8232880
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Heredo-ataxia in a large Dutch pedigree. M.R.I. findings.
Vliegenthart WE; Vielvoye GJ; Kuyt LP
Clin Neurol Neurosurg; 1991; 93(4):275-81. PubMed ID: 1665760
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Familial ataxia with extreme difference in age of clinical onset.
Amit R; Granit G; Shapira Y
Neuropediatrics; 1986 Aug; 17(3):165-7. PubMed ID: 3463881
[TBL] [Abstract][Full Text] [Related]
8. Cerebellar ataxia, dementia, pyramidal signs, cortical cataract of the posterior pole and a raised IgG index in a patient with a sporadic form of olivopontocerebellar atrophy.
Schelhaas HJ; Hageman G; Post JG
Clin Neurol Neurosurg; 1997 May; 99(2):99-101. PubMed ID: 9213052
[TBL] [Abstract][Full Text] [Related]
9. Single photon emission computed tomography using N-isopropyl-p-[123I]iodoamphetamine in spinocerebellar degeneration.
Ohkoshi N; Ishii A; Shoji S
Eur Neurol; 1995; 35(3):156-61. PubMed ID: 7628495
[TBL] [Abstract][Full Text] [Related]
10. Genetic heterogeneity of dominantly inherited olivopontocerebellar atrophy (OPCA) in the Japanese: linkage study of two pedigrees and evidence for the disease locus on chromosome 12q (SCA2).
Ihara T; Sasaki H; Wakisaka A; Takada A; Yoshiki T; Matsuura T; Hamada T; Suzuki Y; Tashiro K
Jpn J Hum Genet; 1994 Sep; 39(3):305-13. PubMed ID: 7841441
[TBL] [Abstract][Full Text] [Related]
11. Brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophy.
Kish SJ; Currier RD; Schut L; Perry TL; Morito CL
Ann Neurol; 1987 Aug; 22(2):272-5. PubMed ID: 3477997
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Multivariate analysis of the clinical signs in late cortical cerebellar atrophy (LCCA) in Japan--compared with olivo-ponto-cerebellar atrophy (OPCA) and hereditary cortical cerebellar atrophy (HCCA)].
Yanagimoto S; Takayanagi T; Hirayama K; Nakamura R; Yanagisawa N
Rinsho Shinkeigaku; 1992 Sep; 32(9):951-5. PubMed ID: 1300266
[TBL] [Abstract][Full Text] [Related]
14. Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.
Rich SS; Wilkie P; Schut L; Vance G; Orr HT
Am J Hum Genet; 1987 Oct; 41(4):524-31. PubMed ID: 3477955
[TBL] [Abstract][Full Text] [Related]
15. Clinical study of large kindreds with autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) of late onset.
Spadaro M; Giunti P; Colazza GB; Naso F; Bianco F; Morocutti C
Ital J Neurol Sci; 1993 Jan; 14(1):17-21. PubMed ID: 8473149
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. X-linked olivopontocerebellar atrophy.
Lutz R; Bodensteiner J; Schaefer B; Gay C
Clin Genet; 1989 Jun; 35(6):417-22. PubMed ID: 2661059
[TBL] [Abstract][Full Text] [Related]
18. Heterogeneous findings in four cases of cerebellar ataxia associated with hypogonadism (Holmes' type ataxia).
De Michele G; Filla A; Striano S; Rimoldi M; Campanella G
Clin Neurol Neurosurg; 1993 Mar; 95(1):23-8. PubMed ID: 8453811
[TBL] [Abstract][Full Text] [Related]
19. Argentophilic intracytoplasmic inclusions in multiple system atrophy.
Mochizuki A; Mizusawa H; Ohkoshi N; Yoshizawa K; Komatsuzaki Y; Inoue K; Kanazawa I
J Neurol; 1992 Jul; 239(6):311-6. PubMed ID: 1380981
[TBL] [Abstract][Full Text] [Related]
20. [Linkage analysis of hereditary spinocerebellar degeneration].
Wakisaka A; Sasaki H
Tanpakushitsu Kakusan Koso; 1993 Feb; 38(3):346-53. PubMed ID: 8098158
[No Abstract] [Full Text] [Related]
[Next] [New Search]