200 related articles for article (PubMed ID: 18325672)
21. Lethal form of spinocerebellar ataxia type 7 with early onset in childhood.
Gousse G; Patural H; Touraine R; Chabrier S; Rolland E; Antoine JC; Perrin L
Arch Pediatr; 2018 Jan; 25(1):42-44. PubMed ID: 29248324
[TBL] [Abstract][Full Text] [Related]
22. Spinocerebellar ataxia type 7 cerebellar disease requires the coordinated action of mutant ataxin-7 in neurons and glia, and displays non-cell-autonomous bergmann glia degeneration.
Furrer SA; Mohanachandran MS; Waldherr SM; Chang C; Damian VA; Sopher BL; Garden GA; La Spada AR
J Neurosci; 2011 Nov; 31(45):16269-78. PubMed ID: 22072678
[TBL] [Abstract][Full Text] [Related]
23. Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report).
Bouzid FZ; Mansouri M; Abdelaziz C; Louhab N; Bernard S; Strubi-Vuillaume I; Dafir K; Aboussair N
Pan Afr Med J; 2021; 38():162. PubMed ID: 33995769
[TBL] [Abstract][Full Text] [Related]
24. Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2.
Wang C; Xu Y; Feng X; Ma J; Xie S; Zhang Y; Tang BS; Chan P
Neurobiol Aging; 2015 Jan; 36(1):545.e1-7. PubMed ID: 25189117
[TBL] [Abstract][Full Text] [Related]
25. Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12.
Srivastava AK; Choudhry S; Gopinath MS; Roy S; Tripathi M; Brahmachari SK; Jain S
Ann Neurol; 2001 Dec; 50(6):796-800. PubMed ID: 11761478
[TBL] [Abstract][Full Text] [Related]
26. [Molecular genetic diagnosis and clinical analysis of spinocerebellar ataxia type 7].
Xie QY; Liang XL; Li XH; Feng YQ
Di Yi Jun Yi Da Xue Xue Bao; 2004 Jan; 24(1):62-5. PubMed ID: 14724100
[TBL] [Abstract][Full Text] [Related]
27. Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases.
Wang J; Shen L; Lei L; Xu Q; Zhou J; Liu Y; Guan W; Pan Q; Xia K; Tang B; Jiang H
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Jun; 36(6):482-9. PubMed ID: 21743138
[TBL] [Abstract][Full Text] [Related]
28. Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families.
García-Velázquez LE; Canizales-Quinteros S; Romero-Hidalgo S; Ochoa-Morales A; Martínez-Ruano L; Márquez-Luna C; Acuña-Alonzo V; Villarreal-Molina MT; Alonso-Vilatela ME; Yescas-Gómez P
Neurogenetics; 2014 Mar; 15(1):13-7. PubMed ID: 24374739
[TBL] [Abstract][Full Text] [Related]
29. Macular degeneration associated with aberrant expansion of trinucleotide repeat of the SCA7 gene in 2 Japanese families.
Abe T; Tsuda T; Yoshida M; Wada Y; Kano T; Itoyama Y; Tamai M
Arch Ophthalmol; 2000 Oct; 118(10):1415-21. PubMed ID: 11030825
[TBL] [Abstract][Full Text] [Related]
30. The hereditary adult-onset ataxias in South Africa.
Bryer A; Krause A; Bill P; Davids V; Bryant D; Butler J; Heckmann J; Ramesar R; Greenberg J
J Neurol Sci; 2003 Dec; 216(1):47-54. PubMed ID: 14607302
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population.
Magaña JJ; Gómez R; Maldonado-Rodríguez M; Velázquez-Pérez L; Tapia-Guerrero YS; Cortés H; Leyva-García N; Hernández-Hernández O; Cisneros B
Cerebellum; 2013 Dec; 12(6):902-5. PubMed ID: 23828024
[TBL] [Abstract][Full Text] [Related]
33. Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10.
Raskin S; Ashizawa T; Teive HA; Arruda WO; Fang P; Gao R; White MC; Werneck LC; Roa B
Arch Neurol; 2007 Apr; 64(4):591-4. PubMed ID: 17420323
[TBL] [Abstract][Full Text] [Related]
34. Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy.
Michalik A; Martin JJ; Van Broeckhoven C
Eur J Hum Genet; 2004 Jan; 12(1):2-15. PubMed ID: 14571264
[TBL] [Abstract][Full Text] [Related]
35. Clinical and genetic study of a Chinese family with spinocerebellar ataxia type 7.
Han Y; Deng B; Liu M; Jiang J; Wu S; Guan Y
Neurol India; 2010; 58(4):622-6. PubMed ID: 20739808
[TBL] [Abstract][Full Text] [Related]
36. Molecular Mechanisms and Therapeutic Strategies in Spinocerebellar Ataxia Type 7.
Karam A; Trottier Y
Adv Exp Med Biol; 2018; 1049():197-218. PubMed ID: 29427104
[TBL] [Abstract][Full Text] [Related]
37. Cell biology of spinocerebellar ataxia.
Orr HT
J Cell Biol; 2012 Apr; 197(2):167-77. PubMed ID: 22508507
[TBL] [Abstract][Full Text] [Related]
38. Identification of the spinocerebellar ataxia type 7 mutation in Taiwan: application of PCR-based Southern blot.
Hsieh M; Lin SJ; Chen JF; Lin HM; Hsiao KM; Li SY; Li C; Tsai CJ
J Neurol; 2000 Aug; 247(8):623-9. PubMed ID: 11041330
[TBL] [Abstract][Full Text] [Related]
39. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy.
Cellini E; Nacmias B; Forleo P; Piacentini S; Guarnieri BM; Serio A; Calabrò A; Renzi D; Sorbi S
Arch Neurol; 2001 Nov; 58(11):1856-9. PubMed ID: 11708995
[TBL] [Abstract][Full Text] [Related]
40. Very large (CAG)(n) DNA repeat expansions in the sperm of two spinocerebellar ataxia type 7 males.
Monckton DG; Cayuela ML; Gould FK; Brock GJ; Silva R; Ashizawa T
Hum Mol Genet; 1999 Dec; 8(13):2473-8. PubMed ID: 10556295
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]