192 related articles for article (PubMed ID: 8091082)
1. [Molecular genetics and familial ataxia].
Koenig M; Sirugo G; Duclos F
Rev Neurol (Paris); 1993; 149(11):698-702. PubMed ID: 8091082
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetics of hereditary ataxias.
Banfi S; Zoghbi HY
Baillieres Clin Neurol; 1994 Aug; 3(2):281-95. PubMed ID: 7952848
[TBL] [Abstract][Full Text] [Related]
3. Distinct phenotypes within autosomal recessive ataxias not linked to already known loci.
Bouhlal Y; El-Euch-Fayeche G; Amouri R; Hentati F
Acta Myol; 2005 Oct; 24(2):155-61. PubMed ID: 16550933
[TBL] [Abstract][Full Text] [Related]
4. Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
Gros-Louis F; Dupré N; Dion P; Fox MA; Laurent S; Verreault S; Sanes JR; Bouchard JP; Rouleau GA
Nat Genet; 2007 Jan; 39(1):80-5. PubMed ID: 17159980
[TBL] [Abstract][Full Text] [Related]
5. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.
Thiffault I; Rioux MF; Tetreault M; Jarry J; Loiselle L; Poirier J; Gros-Louis F; Mathieu J; Vanasse M; Rouleau GA; Bouchard JP; Lesage J; Brais B
Brain; 2006 Sep; 129(Pt 9):2332-40. PubMed ID: 16672289
[TBL] [Abstract][Full Text] [Related]
6. [Genetics of peripheral neuropathies and hereditary ataxias].
Palau F; Sevilla T
Neurologia; 1995 Dec; 10 Suppl 1():32-43. PubMed ID: 8838557
[TBL] [Abstract][Full Text] [Related]
7. Autosomal recessive cerebellar ataxias.
Palau F; Espinós C
Orphanet J Rare Dis; 2006 Nov; 1():47. PubMed ID: 17112370
[TBL] [Abstract][Full Text] [Related]
8. [Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology].
Espinós-Armero C; González-Cabo P; Palau-Martínez F
Rev Neurol; 2005 Oct 1-15; 41(7):409-22. PubMed ID: 16193447
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
Hamza W; Ali Pacha L; Hamadouche T; Muller J; Drouot N; Ferrat F; Makri S; Chaouch M; Tazir M; Koenig M; Benhassine T
BMC Med Genet; 2015 Jun; 16():36. PubMed ID: 26068213
[TBL] [Abstract][Full Text] [Related]
11. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
12. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
Ben Hamida M; Attia-Romdhane N; Triki CH; Oueslati S; Hentati F
Rev Neurol (Paris); 1991; 147(12):798-808. PubMed ID: 1780608
[TBL] [Abstract][Full Text] [Related]
13. [Molecular genetics of inherited neuropathies].
Takashima H
Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
[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. [Hereditary ataxias].
Tallaksen CM
Tidsskr Nor Laegeforen; 2008 Sep; 128(17):1977-80. PubMed ID: 18787576
[TBL] [Abstract][Full Text] [Related]
16. Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy and peripheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23.
Bomont P; Watanabe M; Gershoni-Barush R; Shizuka M; Tanaka M; Sugano J; Guiraud-Chaumeil C; Koenig M
Eur J Hum Genet; 2000 Dec; 8(12):986-90. PubMed ID: 11175288
[TBL] [Abstract][Full Text] [Related]
17. "Acadian" and "classical" forms of Friedreich ataxia are most probably caused by mutations at the same locus.
Keats BJ; Ward LJ; Shaw J; Wickremasinghe A; Chamberlain S
Am J Med Genet; 1989 Jun; 33(2):266-8. PubMed ID: 2764036
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Friedreich ataxia in Acadian families from eastern Canada: clinical diversity with conserved haplotypes.
Richter A; Poirier J; Mercier J; Julien D; Morgan K; Roy M; Gosselin F; Bouchard JP; Melançon SB
Am J Med Genet; 1996 Sep; 64(4):594-601. PubMed ID: 8870928
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
