337 related articles for article (PubMed ID: 8154871)
1. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.
Benomar A; Le Guern E; Dürr A; Ouhabi H; Stevanin G; Yahyaoui M; Chkili T; Agid Y; Brice A
Ann Neurol; 1994 Apr; 35(4):439-44. PubMed ID: 8154871
[TBL] [Abstract][Full Text] [Related]
2. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.
Benomar A; Krols L; Stevanin G; Cancel G; LeGuern E; David G; Ouhabi H; Martin JJ; Dürr A; Zaim A
Nat Genet; 1995 May; 10(1):84-8. PubMed ID: 7647798
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
Verbeek DS; Schelhaas JH; Ippel EF; Beemer FA; Pearson PL; Sinke RJ
Hum Genet; 2002 Oct; 111(4-5):388-93. PubMed ID: 12384780
[TBL] [Abstract][Full Text] [Related]
4. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan.
Hayashi M; Adachi Y; Mori M; Nakano T; Nakashima K
Acta Neurol Scand; 2007 Aug; 116(2):123-7. PubMed ID: 17661799
[TBL] [Abstract][Full Text] [Related]
5. Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1.
Holmberg M; Johansson J; Forsgren L; Heijbel J; Sandgren O; Holmgren G
Hum Mol Genet; 1995 Aug; 4(8):1441-5. PubMed ID: 7581386
[TBL] [Abstract][Full Text] [Related]
6. Exclusion of linkage between D3S47 (C17) and ADRPII gene in two large families of moderate autosomal dominant retinitis pigmentosa: evidence for genetic heterogeneity.
Kaplan J; Guasconi G; Dufier JL; Michel-Awad A; David A; Munnich A; Frezal J
Ann Genet; 1990; 33(3):152-4. PubMed ID: 2288459
[TBL] [Abstract][Full Text] [Related]
7. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.
Onodera Y; Aoki M; Mizuno H; Warita H; Shiga Y; Itoyama Y
Neurology; 2006 Oct; 67(7):1300-2. PubMed ID: 17030774
[TBL] [Abstract][Full Text] [Related]
8. 16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.
Ouyang Y; Sakoe K; Shimazaki H; Namekawa M; Ogawa T; Ando Y; Kawakami T; Kaneko J; Hasegawa Y; Yoshizawa K; Amino T; Ishikawa K; Mizusawa H; Nakano I; Takiyama Y
J Neurol Sci; 2006 Sep; 247(2):180-6. PubMed ID: 16780885
[TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1.
Jöbsis GJ; Weber JW; Barth PG; Keizers H; Baas F; van Schooneveld MJ; van Hilten JJ; Troost D; Geesink HH; Bolhuis PA
J Neurol Neurosurg Psychiatry; 1997 Apr; 62(4):367-71. PubMed ID: 9120450
[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. SCA2 is not a major locus for ADCA type I in French families.
Cancel G; Stevanin G; Dürr A; Chneiweiss H; Penet C; Pothin Y; Agid Y; Brice A
Am J Med Genet; 1995 Oct; 60(5):382-5. PubMed ID: 8546150
[TBL] [Abstract][Full Text] [Related]
12. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.
Gispert S; Twells R; Orozco G; Brice A; Weber J; Heredero L; Scheufler K; Riley B; Allotey R; Nothers C
Nat Genet; 1993 Jul; 4(3):295-9. PubMed ID: 8358438
[TBL] [Abstract][Full Text] [Related]
13. Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.
Verbeek DS; van de Warrenburg BP; Wesseling P; Pearson PL; Kremer HP; Sinke RJ
Brain; 2004 Nov; 127(Pt 11):2551-7. PubMed ID: 15306549
[TBL] [Abstract][Full Text] [Related]
14. Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.
Li M; Ishikawa K; Toru S; Tomimitsu H; Takashima M; Goto J; Takiyama Y; Sasaki H; Imoto I; Inazawa J; Toda T; Kanazawa I; Mizusawa H
J Hum Genet; 2003; 48(3):111-8. PubMed ID: 12624721
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 7614088
[TBL] [Abstract][Full Text] [Related]
16. A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan.
Takashima M; Ishikawa K; Nagaoka U; Shoji S; Mizusawa H
J Hum Genet; 2001; 46(4):167-71. PubMed ID: 11322654
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.
Infante J; Combarros O; Volpini V; Corral J; Llorca J; Berciano J
Acta Neurol Scand; 2005 Jun; 111(6):391-9. PubMed ID: 15876341
[TBL] [Abstract][Full Text] [Related]
18. Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.
Olsson JE; Samanns C; Jimenez J; Pongratz J; Chand A; Watty A; Seuchter SA; Denton M; Gal A
Am J Med Genet; 1990 Apr; 35(4):595-9. PubMed ID: 2333895
[TBL] [Abstract][Full Text] [Related]
19. A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.
Owada K; Ishikawa K; Toru S; Ishida G; Gomyoda M; Tao O; Noguchi Y; Kitamura K; Kondo I; Noguchi E; Arinami T; Mizusawa H
Neurology; 2005 Aug; 65(4):629-32. PubMed ID: 16116133
[TBL] [Abstract][Full Text] [Related]
20. Genetics of the SCA6 gene in a large family segregating an autosomal dominant "pure" cerebellar ataxia.
García-Planells J; Cuesta A; Vilchez JJ; Martínez F; Prieto F; Palau F
J Med Genet; 1999 Feb; 36(2):148-51. PubMed ID: 10051016
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
