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Results: 1 to 20 of 93

Related Articles by Review for PubMed (Select 11448300)

2.

The molecular biology of the autosomal-dominant cerebellar ataxias.

Klockgether T, Wüllner U, Spauschus A, Evert B.

Mov Disord. 2000 Jul;15(4):604-12. Review.

PMID:
10928570
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.

Molecular genetics of hereditary ataxias.

Banfi S, Zoghbi HY.

Baillieres Clin Neurol. 1994 Aug;3(2):281-95. Review.

PMID:
7952848
5.

[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
6.

The wide spectrum of spinocerebellar ataxias (SCAs).

Manto MU.

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

PMID:
15895552
7.

[Autosomal dominant spinocerebellar ataxia].

Legros B, Manto MU.

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

PMID:
10672773
8.
9.

The hereditary spinocerebellar ataxias in Japan.

Sasaki H, Yabe I, Tashiro K.

Cytogenet Genome Res. 2003;100(1-4):198-205. Review.

PMID:
14526181
10.

Genes implicated in the pathogenesis of spinocerebellar ataxias.

Wüllner U.

Drugs Today (Barc). 2003 Dec;39(12):927-37. Review.

PMID:
14747838
11.

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
12.

[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
13.
14.

Molecular genetics of spinocerebellar ataxia type 8 (SCA8).

Mutsuddi M, Rebay I.

RNA Biol. 2005 Apr;2(2):49-52. Epub 2005 Apr 25. Review.

PMID:
17132942
15.

Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.

Damji KF, Allingham RR, Pollock SC, Small K, Lewis KE, Stajich JM, Yamaoka LH, Vance JM, Pericak-Vance MA.

Arch Neurol. 1996 Apr;53(4):338-44. Review.

PMID:
8929156
16.

[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
17.

The hereditary ataxias.

Koeppen AH.

J Neuropathol Exp Neurol. 1998 Jun;57(6):531-43. Review.

PMID:
9630233
18.

Machado-Joseph disease.

Sudarsky L, Coutinho P.

Clin Neurosci. 1995;3(1):17-22. Review.

PMID:
7614089
19.

Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I.

Rivaud-Pechoux S, Dürr A, Gaymard B, Cancel G, Ploner CJ, Agid Y, Brice A, Pierrot-Deseilligny C.

Ann Neurol. 1998 Mar;43(3):297-302. Review.

PMID:
9506545
20.

Machado-Joseph disease and other rare spinocerebellar ataxias.

Matilla-Dueñas A.

Adv Exp Med Biol. 2012;724:172-88. doi: 10.1007/978-1-4614-0653-2_14. Review.

PMID:
22411243
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