149 related articles for article (PubMed ID: 9710044)
21. 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]
22. Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).
David G; Dürr A; Stevanin G; Cancel G; Abbas N; Benomar A; Belal S; Lebre AS; Abada-Bendib M; Grid D; Holmberg M; Yahyaoui M; Hentati F; Chkili T; Agid Y; Brice A
Hum Mol Genet; 1998 Feb; 7(2):165-70. PubMed ID: 9425222
[TBL] [Abstract][Full Text] [Related]
23. CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity.
Gambardella A; Annesi G; Bono F; Spadafora P; Valentino P; Pasqua AA; Mazzei R; Montesanti R; Conforti FL; Oliveri RL; Zappia M; Aguglia U; Quattrone A
J Neurol; 1998 Oct; 245(10):647-52. PubMed ID: 9776463
[TBL] [Abstract][Full Text] [Related]
24. Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation.
Johansson J; Forsgren L; Sandgren O; Brice A; Holmgren G; Holmberg M
Hum Mol Genet; 1998 Feb; 7(2):171-6. PubMed ID: 9425223
[TBL] [Abstract][Full Text] [Related]
25. [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]
26. SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene.
Riess O; Schöls L; Bottger H; Nolte D; Vieira-Saecker AM; Schimming C; Kreuz F; Macek M; Krebsová A; Macek M Sen ; Klockgether T; Zühlke C; Laccone FA
Hum Mol Genet; 1997 Aug; 6(8):1289-93. PubMed ID: 9259275
[TBL] [Abstract][Full Text] [Related]
27. Clinical and molecular features of spinocerebellar ataxia type 6.
Stevanin G; Dürr A; David G; Didierjean O; Cancel G; Rivaud S; Tourbah A; Warter JM; Agid Y; Brice A
Neurology; 1997 Nov; 49(5):1243-6. PubMed ID: 9371901
[TBL] [Abstract][Full Text] [Related]
28. Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.
Cancel G; Dürr A; Didierjean O; Imbert G; Bürk K; Lezin A; Belal S; Benomar A; Abada-Bendib M; Vial C; Guimarães J; Chneiweiss H; Stevanin G; Yvert G; Abbas N; Saudou F; Lebre AS; Yahyaoui M; Hentati F; Vernant JC; Klockgether T; Mandel JL; Agid Y; Brice A
Hum Mol Genet; 1997 May; 6(5):709-15. PubMed ID: 9158145
[TBL] [Abstract][Full Text] [Related]
29. 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. PubMed ID: 9874485
[TBL] [Abstract][Full Text] [Related]
30. Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).
Matsuyama Z; Kawakami H; Maruyama H; Izumi Y; Komure O; Udaka F; Kameyama M; Nishio T; Kuroda Y; Nishimura M; Nakamura S
Hum Mol Genet; 1997 Aug; 6(8):1283-7. PubMed ID: 9259274
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. [Spinocerebellar ataxia: advances in genetic research and its clinical implication].
Sasaki H
Hokkaido Igaku Zasshi; 1997 Jan; 72(1):13-20. PubMed ID: 9086358
[TBL] [Abstract][Full Text] [Related]
33. An expanded CAG repeat sequence in spinocerebellar ataxia type 7.
Lindblad K; Savontaus ML; Stevanin G; Holmberg M; Digre K; Zander C; Ehrsson H; David G; Benomar A; Nikoskelainen E; Trottier Y; Holmgren G; Ptacek LJ; Anttinen A; Brice A; Schalling M
Genome Res; 1996 Oct; 6(10):965-71. PubMed ID: 8908515
[TBL] [Abstract][Full Text] [Related]
34. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
[TBL] [Abstract][Full Text] [Related]
35. Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.
Ranum LP; Chung MY; Banfi S; Bryer A; Schut LJ; Ramesar R; Duvick LA; McCall A; Subramony SH; Goldfarb L
Am J Hum Genet; 1994 Aug; 55(2):244-52. PubMed ID: 8037204
[TBL] [Abstract][Full Text] [Related]
36. Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations.
Geschwind DH; Perlman S; Figueroa KP; Karrim J; Baloh RW; Pulst SM
Neurology; 1997 Nov; 49(5):1247-51. PubMed ID: 9371902
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. The CAG repeats number of spinocerebellar ataxia type 1 gene in normal Taiwanese and in patients with dominant inherited ataxia.
Hsieh ML; Yang CY; Tsai HF; Chen YY; Li C; Li SY
Proc Natl Sci Counc Repub China B; 1997 Jul; 21(3):91-5. PubMed ID: 9309871
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan.
Kameya T; Abe K; Aoki M; Sahara M; Tobita M; Konno H; Itoyama Y
Neurology; 1995 Aug; 45(8):1587-94. PubMed ID: 7543989
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
