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Items: 1 to 20 of 21

1.

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.

Imbert G, Saudou F, Yvert G, Devys D, Trottier Y, Garnier JM, Weber C, Mandel JL, Cancel G, Abbas N, Dürr A, Didierjean O, Stevanin G, Agid Y, Brice A.

Nat Genet. 1996 Nov;14(3):285-91.

PMID:
8896557
2.

Spinocerebellar ataxia type 1.

Zoghbi HY.

Clin Neurosci. 1995;3(1):5-11. Review.

PMID:
7614095
3.

[Molecular analyses of intergenerational instability of CAG repeat in SCA2 gene].

Igarashi S, Tsuji S.

Nihon Rinsho. 1999 Apr;57(4):811-7. Review. Japanese.

PMID:
10222771
4.

The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.

Koshy BT, Zoghbi HY.

Brain Pathol. 1997 Jul;7(3):927-42. Review.

PMID:
9217976
5.

The unstable trinucleotide repeat story of major psychosis.

Vincent JB, Paterson AD, Strong E, Petronis A, Kennedy JL.

Am J Med Genet. 2000 Spring;97(1):77-97. Review.

PMID:
10813808
6.

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.

PMID:
9874485
7.

Spinocerebellar ataxia type 1.

Zoghbi HY, Orr HT.

Semin Cell Biol. 1995 Feb;6(1):29-35. Review.

PMID:
7620119
8.

[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
9.

Analysis of the CAG repeat and gene product in spinocerebellar ataxia type 1.

Zoghbi HY.

Proc Assoc Am Physicians. 1995 Jul;107(2):231-6. Review. No abstract available.

PMID:
8624857
10.

Infantile onset spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases.

Singh A, Faruq M, Mukerji M, Dwivedi MK, Pruthi S, Kapoor S.

J Child Neurol. 2014 Jan;29(1):139-44. doi: 10.1177/0883073813509015. Epub 2013 Dec 2. Review.

PMID:
24300164
11.

[Molecular basis of heterogeneities of clinical presentation of dentatorubral pallidoluysian atrophy (DRPLA)].

Tsuji S.

Rinsho Shinkeigaku. 1994 Dec;34(12):1227-9. Review. Japanese.

PMID:
7774119
12.

[Clinical and genetic characteristics of SCA1].

Abe K.

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

PMID:
10222768
13.

[Correlation of clinichopathological features and CAG repeats in SCA2].

Koyano S, Iwabuchi K.

Nihon Rinsho. 1999 Apr;57(4):805-10. Review. Japanese.

PMID:
10222770
14.

Trinucleotide repeat expansions and human genetic disease.

Bates G, Lehrach H.

Bioessays. 1994 Apr;16(4):277-84. Review.

PMID:
8031305
16.
17.
18.

Molecular genetics and neurobiology of neurodegenerative and neurodevelopmental disorders.

Zoghbi HY.

Pediatr Res. 1997 May;41(5):722-6. Review. No abstract available.

PMID:
9128297
19.

[Genetic diagnosis of hereditary spinocerebellar degeneration].

Ikeuchi T, Tsuji S.

Nihon Naika Gakkai Zasshi. 1994 Nov 10;83(11):2000-6. Review. Japanese. No abstract available.

PMID:
7852812
20.

[Diseases in the field of internal medicine and gene abnormalities. 5. Nervous system diseases--molecular genetics of hereditary spinocerebellar degeneration].

Tsuji S.

Nihon Naika Gakkai Zasshi. 1996 Sep 10;85(9):1514-9. Review. Japanese. No abstract available.

PMID:
8999100

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