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Items: 1 to 20 of 27

1.

A clinical, genetic, neuropathological study in a Japanese family with SCA 6 and a review of Japanese autopsy cases of autosomal dominant cortical cerebellar atrophy.

Tsuchiya K, Ishikawa K, Watabiki S, Tone O, Taki K, Haga C, Takashima M, Ito U, Okeda R, Mizusawa H, Ikeda K.

J Neurol Sci. 1998 Sep 18;160(1):54-9. Review.

PMID:
9804117
2.
3.

Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.

Pascual-Castroviejo I, Gutierrez M, Morales C, Gonzalez-Mediero I, Martínez-Bermejo A, Pascual-Pascual SI.

Neuropediatrics. 1994 Aug;25(4):183-90. Review.

PMID:
7824090
4.

[Autosomal dominant spinocerebellar degeneration--new forms and pathomechanisms].

Mizusawa H.

Rinsho Shinkeigaku. 2004 Nov;44(11):782-4. Review. Japanese.

PMID:
15651290
5.

[An autopsied case of idiopathic late cortical cerebellar atrophy--comparison with other cortical cerebellar atrophy].

Iwabuchi K, Yagishita S.

Rinsho Shinkeigaku. 1990 Nov;30(11):1190-6. Review. Japanese.

PMID:
2085923
6.

[Autosomal dominant spinocerebellar ataxia].

Legros B, Manto MU.

Rev Med Brux. 1999 Dec;20(6):495-503. Review. French.

PMID:
10672773
7.

[An autopsy case of hereditary cerebellar atrophy (Holmes-type) with mental symptoms and rhythmic skeletal myoclonus].

Ohta S, Mizutani Y, Anno M.

No To Shinkei. 1994 Jul;46(7):663-70. Review. Japanese.

PMID:
7946622
8.

Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations.

Iwabuchi K, Tsuchiya K, Uchihara T, Yagishita S.

Rev Neurol (Paris). 1999 Apr;155(4):255-70. Review.

PMID:
10367323
9.
10.

Molecular pathology of dentatorubral-pallidoluysian atrophy.

Kanazawa I.

Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29;354(1386):1069-74. Review.

11.

[Autosomal dominant cortical cerebellar atrophy (ADCCA) linked to chromosome 16q].

Ishikawa K.

Rinsho Shinkeigaku. 2001 Dec;41(12):1117-9. Review. Japanese.

PMID:
12235813
12.

Autosomal dominant spinocerebellar atrophy with retinal degeneration.

Ptácek LJ.

Clin Neurosci. 1995;3(1):28-32. Review.

PMID:
7614091
13.

Sporadic amyotrophic lateral sclerosis of long duration mimicking spinal progressive muscular atrophy exists: additional autopsy case with a clinical course of 19 years.

Tsuchiya K, Sano M, Shiotsu H, Akiyama H, Watabiki S, Taki K, Kondo H, Nakano I, Ikeda K.

Neuropathology. 2004 Sep;24(3):228-35. Review.

PMID:
15484701
14.

[A case of severe involvement of the motor neuron system accompanied with cerebellar ataxia].

Horiuchi I, Furuya H, Yoshimura T, Kobayashi T, Kusunoki S.

Rinsho Shinkeigaku. 1997 Feb;37(2):123-6. Review. Japanese.

PMID:
9164144
15.

The pathogenesis of spinocerebellar ataxia.

Koeppen AH.

Cerebellum. 2005;4(1):62-73. Review.

PMID:
15895563
16.

The wide spectrum of spinocerebellar ataxias (SCAs).

Manto MU.

Cerebellum. 2005;4(1):2-6. Review.

PMID:
15895552
17.

Topographical aspects of cerebellar degeneration.

Voogd J.

Clin Neurol Neurosurg. 1992;94 Suppl:S12-5. Review.

PMID:
1320484
18.

Spinocerebellar ataxia type 14.

Chen DH, Raskind WH, Bird TD.

Handb Clin Neurol. 2012;103:555-9. doi: 10.1016/B978-0-444-51892-7.00036-X. Review.

PMID:
21827914
19.

[Cerebellar imitation synkineses].

Trouillas P, Brudon F, Froment JC, Nighoghossian N, Neuschwander P, Tommasi-Davenas C.

Rev Neurol (Paris). 1990;146(2):107-15. Review. French.

PMID:
2181586
20.

Dominantly inherited congenital cerebellar ataxia with atrophy of the vermis.

Tomiwa K, Baraitser M, Wilson J.

Pediatr Neurol. 1987 Nov-Dec;3(6):360-2. Review.

PMID:
3334022

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