103 related articles for article (PubMed ID: 10222770)
1. [Correlation of clinichopathological features and CAG repeats in SCA2].
Koyano S; Iwabuchi K
Nihon Rinsho; 1999 Apr; 57(4):805-10. PubMed ID: 10222770
[TBL] [Abstract][Full Text] [Related]
2. [The phenotype variation correlates with the size of CAG repeat in SCA2].
Sasaki H; Sanpei K
Nihon Rinsho; 1999 Apr; 57(4):818-21. PubMed ID: 10222772
[TBL] [Abstract][Full Text] [Related]
3. An autopsy case of an aged patient with spinocerebellar ataxia type 2.
Ishida C; Komai K; Yonezawa K; Sakajiri K; Nitta E; Kawashima A; Yamada M
Neuropathology; 2011 Oct; 31(5):510-8. PubMed ID: 21134000
[TBL] [Abstract][Full Text] [Related]
4. [Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)].
Ishikawa K; Mizusawa H
Nihon Rinsho; 1999 Apr; 57(4):880-5. PubMed ID: 10222783
[TBL] [Abstract][Full Text] [Related]
5. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.
Hashida H; Goto J; Kurisaki H; Mizusawa H; Kanazawa I
Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808
[TBL] [Abstract][Full Text] [Related]
6. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese].
Ikeuchi T
Nihon Rinsho; 1999 Apr; 57(4):891-5. PubMed ID: 10222785
[TBL] [Abstract][Full Text] [Related]
7. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
Iwabuchi K; Kogure T; Oda T; Kato Y; Ohtani K; Endo K; Kosaka K; Amano N; Yagishita S
No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
[TBL] [Abstract][Full Text] [Related]
8. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea].
Iwabuchi K; Nakazawa Y; Akai J; Yagishita S; Amano N
No To Shinkei; 1994 Jun; 46(6):563-71. PubMed ID: 8068439
[TBL] [Abstract][Full Text] [Related]
9. [Molecular analyses of intergenerational instability of CAG repeat in SCA2 gene].
Igarashi S; Tsuji S
Nihon Rinsho; 1999 Apr; 57(4):811-7. PubMed ID: 10222771
[TBL] [Abstract][Full Text] [Related]
10. [Clinico-genetic study of type I spinocerebelllar ataxia].
Svetel M; Culjković B; Sternić N; Dragasević B; Stojković I; Romac S; Kostić VS
Srp Arh Celok Lek; 1999; 127(5-6):157-62. PubMed ID: 10500422
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 24300164
[TBL] [Abstract][Full Text] [Related]
12. Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
Ikeuchi T; Takano H; Koide R; Horikawa Y; Honma Y; Onishi Y; Igarashi S; Tanaka H; Nakao N; Sahashi K; Tsukagoshi H; Inoue K; Takahashi H; Tsuji S
Ann Neurol; 1997 Dec; 42(6):879-84. PubMed ID: 9403480
[TBL] [Abstract][Full Text] [Related]
13. An autopsy case of spinocerebellar ataxia type 6 with mental symptoms of schizophrenia and dementia.
Tashiro H; Suzuki SO; Hitotsumatsu T; Iwaki T
Clin Neuropathol; 1999; 18(4):198-204. PubMed ID: 10442462
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 8896557
[TBL] [Abstract][Full Text] [Related]
15. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H
Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
[TBL] [Abstract][Full Text] [Related]
16. Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease.
Lopes-Cendes I; Maciel P; Kish S; Gaspar C; Robitaille Y; Clark HB; Koeppen AH; Nance M; Schut L; Silveira I; Coutinho P; Sequeiros J; Rouleau GA
Ann Neurol; 1996 Aug; 40(2):199-206. PubMed ID: 8773601
[TBL] [Abstract][Full Text] [Related]
17. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.
Sanpei K; Takano H; Igarashi S; Sato T; Oyake M; Sasaki H; Wakisaka A; Tashiro K; Ishida Y; Ikeuchi T; Koide R; Saito M; Sato A; Tanaka T; Hanyu S; Takiyama Y; Nishizawa M; Shimizu N; Nomura Y; Segawa M; Iwabuchi K; Eguchi I; Tanaka H; Takahashi H; Tsuji S
Nat Genet; 1996 Nov; 14(3):277-84. PubMed ID: 8896556
[TBL] [Abstract][Full Text] [Related]
18. [Autopsy cases of hereditary ataxia pathologically diagnosed as the Japanese type of Joseph disease--cliniconeuropathological findings].
Kogure T; Oda T; Katoh Y
Seishin Shinkeigaku Zasshi; 1990; 92(3):161-83. PubMed ID: 2353076
[TBL] [Abstract][Full Text] [Related]
19. [An apparently sporadic case with spinocerebellar ataxia type 1 (SCA1)].
Futamura N; Matsumura R; Murata K; Suzumura A; Takayanagi T
Rinsho Shinkeigaku; 1997 Aug; 37(8):708-10. PubMed ID: 9404150
[TBL] [Abstract][Full Text] [Related]
20. Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.
Goldfarb LG; Vasconcelos O; Platonov FA; Lunkes A; Kipnis V; Kononova S; Chabrashvili T; Vladimirtsev VA; Alexeev VP; Gajdusek DC
Ann Neurol; 1996 Apr; 39(4):500-6. PubMed ID: 8619528
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
