176 related articles for article (PubMed ID: 11445634)
1. A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1.
Miyoshi Y; Yamada T; Tanimura M; Taniwaki T; Arakawa K; Ohyagi Y; Furuya H; Yamamoto K; Sakai K; Sasazuki T; Kira J
Neurology; 2001 Jul; 57(1):96-100. PubMed ID: 11445634
[TBL] [Abstract][Full Text] [Related]
2. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
Chung MY; Lu YC; Cheng NC; Soong BW
Brain; 2003 Jun; 126(Pt 6):1293-9. PubMed ID: 12764052
[TBL] [Abstract][Full Text] [Related]
3. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
Waters MF; Fee D; Figueroa KP; Nolte D; Müller U; Advincula J; Coon H; Evidente VG; Pulst SM
Neurology; 2005 Oct; 65(7):1111-3. PubMed ID: 16135769
[TBL] [Abstract][Full Text] [Related]
4. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
Stevanin G; Bouslam N; Thobois S; Azzedine H; Ravaux L; Boland A; Schalling M; Broussolle E; Dürr A; Brice A
Ann Neurol; 2004 Jan; 55(1):97-104. PubMed ID: 14705117
[TBL] [Abstract][Full Text] [Related]
5. Clinical features and genetic analysis of a new form of spinocerebellar ataxia.
Devos D; Schraen-Maschke S; Vuillaume I; Dujardin K; Nazé P; Willoteaux C; Destée A; Sablonnière B
Neurology; 2001 Jan; 56(2):234-8. PubMed ID: 11160961
[TBL] [Abstract][Full Text] [Related]
6. SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.
Cagnoli C; Mariotti C; Taroni F; Seri M; Brussino A; Michielotto C; Grisoli M; Di Bella D; Migone N; Gellera C; Di Donato S; Brusco A
Brain; 2006 Jan; 129(Pt 1):235-42. PubMed ID: 16251216
[TBL] [Abstract][Full Text] [Related]
7. Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus.
Hara K; Fukushima T; Suzuki T; Shimohata T; Oyake M; Ishiguro H; Hirota K; Miyashita A; Kuwano R; Kurisaki H; Yomono H; Goto J; Kanazawa I; Tsuji S
Neurology; 2004 Feb; 62(4):648-51. PubMed ID: 14981189
[TBL] [Abstract][Full Text] [Related]
8. Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
Hirano R; Takashima H; Okubo R; Tajima K; Okamoto Y; Ishida S; Tsuruta K; Arisato T; Arata H; Nakagawa M; Osame M; Arimura K
Neurogenetics; 2004 Dec; 5(4):215-21. PubMed ID: 15455264
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.
Brkanac Z; Bylenok L; Fernandez M; Matsushita M; Lipe H; Wolff J; Nochlin D; Raskind WH; Bird TD
Arch Neurol; 2002 Aug; 59(8):1291-5. PubMed ID: 12164726
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia.
Schelhaas HJ; Ippel PF; Hageman G; Sinke RJ; van der Laan EN; Beemer FA
J Neurol; 2001 Feb; 248(2):113-20. PubMed ID: 11284128
[TBL] [Abstract][Full Text] [Related]
13. Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia.
Grewal RP; Tayag E; Figueroa KP; Zu L; Durazo A; Nunez C; Pulst SM
Neurology; 1998 Nov; 51(5):1423-6. PubMed ID: 9818872
[TBL] [Abstract][Full Text] [Related]
14. Clinical and genetic analysis of spinocerebellar ataxia type 11.
Johnson J; Wood N; Giunti P; Houlden H
Cerebellum; 2008; 7(2):159-64. PubMed ID: 18418680
[TBL] [Abstract][Full Text] [Related]
15. Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
Stevanin G; Hahn V; Lohmann E; Bouslam N; Gouttard M; Soumphonphakdy C; Welter ML; Ollagnon-Roman E; Lemainque A; Ruberg M; Brice A; Durr A
Arch Neurol; 2004 Aug; 61(8):1242-8. PubMed ID: 15313841
[TBL] [Abstract][Full Text] [Related]
16. Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.
Worth PF; Giunti P; Gardner-Thorpe C; Dixon PH; Davis MB; Wood NW
Am J Hum Genet; 1999 Aug; 65(2):420-6. PubMed ID: 10417284
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families.
Lezin A; Cancel G; Stevanin G; Smadja D; Vernant JC; Dürr A; Martial J; Buisson GG; Bellance R; Chneiweiss H; Agid Y; Brice A
Hum Genet; 1996 May; 97(5):671-6. PubMed ID: 8655151
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus.
Dudding TE; Friend K; Schofield PW; Lee S; Wilkinson IA; Richards RI
Neurology; 2004 Dec; 63(12):2288-92. PubMed ID: 15623688
[TBL] [Abstract][Full Text] [Related]
19. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Brusco A; Gellera C; Cagnoli C; Saluto A; Castucci A; Michielotto C; Fetoni V; Mariotti C; Migone N; Di Donato S; Taroni F
Arch Neurol; 2004 May; 61(5):727-33. PubMed ID: 15148151
[TBL] [Abstract][Full Text] [Related]
20. Hereditary cerebellar ataxia and genetic linkage with HLA.
Kumar D; Blank CE; Gelsthorpe K
Hum Genet; 1986 Apr; 72(4):327-32. PubMed ID: 3457760
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]