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Items: 1 to 20 of 68

1.

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.

Schöls L, Krüger R, Amoiridis G, Przuntek H, Epplen JT, Riess O.

J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):67-73.

2.

[Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)].

Ishikawa K, Mizusawa H.

Nihon Rinsho. 1999 Apr;57(4):880-5. Review. Japanese.

PMID:
10222783
3.

[Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese].

Ikeuchi T.

Nihon Rinsho. 1999 Apr;57(4):891-5. Review. Japanese.

PMID:
10222785
4.

[Spinocerebellar ataxia: advances in genetic research and its clinical implication].

Sasaki H.

Hokkaido Igaku Zasshi. 1997 Jan;72(1):13-20. Review. Japanese.

PMID:
9086358
5.

Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics.

Whaley NR, Fujioka S, Wszolek ZK.

Orphanet J Rare Dis. 2011 May 28;6:33. doi: 10.1186/1750-1172-6-33. Review.

6.

[Autosomal dominant spinocerebellar ataxia].

Legros B, Manto MU.

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

PMID:
10672773
7.

The wide spectrum of spinocerebellar ataxias (SCAs).

Manto MU.

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

PMID:
15895552
8.

A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees. The significance of slow saccades in diagnosis.

Wadia N, Pang J, Desai J, Mankodi A, Desai M, Chamberlain S.

Brain. 1998 Dec;121 ( Pt 12):2341-55. Review.

9.

Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.

Fujioka S, Sundal C, Wszolek ZK.

Orphanet J Rare Dis. 2013 Jan 18;8:14. doi: 10.1186/1750-1172-8-14. Review.

10.

[Molecular genetic approach to spinocerebellar ataxias].

Ishikawa K, Ishiguro T, Takahashi M, Sato N, Amino T, Niimi Y, Mizusawa H.

Rinsho Shinkeigaku. 2009 Nov;49(11):907-9. Review. Japanese.

PMID:
20030245
11.

Clinical and molecular analysis of neurodegenerative diseases.

Abe K.

Tohoku J Exp Med. 1997 Apr;181(4):389-409. Review.

12.

[Electrophysiological findings in patients with SCA6].

Kumagai R, Kaseda Y, Kawakami H, Nakamura S.

Nihon Rinsho. 1999 Apr;57(4):886-90. Review. Japanese.

PMID:
10222784
13.

[The phenotype variation correlates with the size of CAG repeat in SCA2].

Sasaki H, Sanpei K.

Nihon Rinsho. 1999 Apr;57(4):818-21. Review. Japanese.

PMID:
10222772
14.
15.

[Frequencies of triplet repeat disorders in dominantly inherited spinocerebellar ataxia (SCA) in the Japanese].

Sasaki H, Tashiro K.

Nihon Rinsho. 1999 Apr;57(4):787-91. Review. Japanese.

PMID:
10222766
16.

CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci.

Frontali M, Novelletto A, Annesi G, Jodice C.

Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29;354(1386):1089-94. Review.

17.

Recent results in ataxia research.

Giunti P, Spadaro M, Colazza GB, Morocutti C.

Riv Neurol. 1991 Jul-Aug;61(4):154-7. Review.

PMID:
1815314
18.

[Clinical and genetic characteristics of SCA1].

Abe K.

Nihon Rinsho. 1999 Apr;57(4):796-800. Review. Japanese.

PMID:
10222768
19.

Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2).

Dürr A, Brice A, Lepage-Lezin A, Cancel G, Smadja D, Vernant JC, Agid Y.

Clin Neurosci. 1995;3(1):12-6. Review.

PMID:
7614088
20.

Autosomal dominant cerebellar ataxias.

Marelli C, Cazeneuve C, Brice A, Stevanin G, Dürr A.

Rev Neurol (Paris). 2011 May;167(5):385-400. doi: 10.1016/j.neurol.2011.01.015. Epub 2011 May 5. Review.

PMID:
21546047
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