164 related articles for article (PubMed ID: 9213052)
1. 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]
2. Olivopontocerebellar atrophy presenting with stridor.
Sundar U; Sharma A; Arekar MA; Vimal P; Yeolekar ME
J Assoc Physicians India; 2003 Aug; 51():813-5. PubMed ID: 14651147
[TBL] [Abstract][Full Text] [Related]
3. The relationship of multiple system atrophy to sporadic olivopontocerebellar atrophy and other forms of idiopathic late-onset cerebellar atrophy.
Gilman S; Quinn NP
Neurology; 1996 May; 46(5):1197-9. PubMed ID: 8628452
[No Abstract] [Full Text] [Related]
4. 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]
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. 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]
7. 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]
8. 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]
9. Olivopontocerebellar atrophy: MR diagnosis and relationship to multisystem atrophy.
Savoiardo M; Strada L; Girotti F; Zimmerman RA; Grisoli M; Testa D; Petrillo R
Radiology; 1990 Mar; 174(3 Pt 1):693-6. PubMed ID: 2305051
[TBL] [Abstract][Full Text] [Related]
10. Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea.
Fox SH; Nieves A; Bergeron C; Lang AE
Mov Disord; 2003 Dec; 18(12):1550-4. PubMed ID: 14673899
[TBL] [Abstract][Full Text] [Related]
11. [Striatonigral degeneration and sporadic olivopontocerebellar atrophy: a consideration of the clinical entity of multiple system atrophy].
Miwa H; Kondo T; Mizuno Y
No To Shinkei; 1999 Apr; 51(4):305-12. PubMed ID: 10363264
[TBL] [Abstract][Full Text] [Related]
12. [Clinical types of spinocerebellar degeneration and evaluation with MR imaging].
Kojima S
Rinsho Shinkeigaku; 1993 Dec; 33(12):1294-6. PubMed ID: 8174328
[TBL] [Abstract][Full Text] [Related]
13. [Olivopontocerebellar atrophy as an important differential diagnosis in atactic gait disorders in elderly patients].
Waespe W; Hayek J; Wichmann W; Bader JP
Schweiz Med Wochenschr; 1988 Jul; 118(27-28):1032-8. PubMed ID: 3166204
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. MRI and CT features of cerebellar degeneration.
Huang YP; Tuason MY; Wu T; Plaitakis A
J Formos Med Assoc; 1993 Jun; 92(6):494-508. PubMed ID: 8106035
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. 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]
18. [Man aged 49 years suffering from progressive clinical picture with palatal tremor, segmental myoclonus, ataxia, parkinsonism, amyotrophy, pyramidal signs, supranuclear ophthalmoplegia and cognitive decline].
Berciano J; Montón FI; Maeso MC; Ferrer I
Neurologia; 2002 May; 17(5):237-43. PubMed ID: 12031213
[TBL] [Abstract][Full Text] [Related]
19. Supratentorial atrophy in spinocerebellar ataxia type 2: MRI study of 20 patients.
Giuffrida S; Saponara R; Restivo DA; Trovato Salinaro A; Tomarchio L; Pugliares P; Fabbri G; Maccagnano C
J Neurol; 1999 May; 246(5):383-8. PubMed ID: 10399871
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]