244 related articles for article (PubMed ID: 25476002)
1. Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion.
Obayashi M; Stevanin G; Synofzik M; Monin ML; Duyckaerts C; Sato N; Streichenberger N; Vighetto A; Desestret V; Tesson C; Wichmann HE; Illig T; Huttenlocher J; Kita Y; Izumi Y; Mizusawa H; Schöls L; Klopstock T; Brice A; Ishikawa K; Dürr A
J Neurol Neurosurg Psychiatry; 2015 Sep; 86(9):986-95. PubMed ID: 25476002
[TBL] [Abstract][Full Text] [Related]
2. Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.
Kobayashi H; Abe K; Matsuura T; Ikeda Y; Hitomi T; Akechi Y; Habu T; Liu W; Okuda H; Koizumi A
Am J Hum Genet; 2011 Jul; 89(1):121-30. PubMed ID: 21683323
[TBL] [Abstract][Full Text] [Related]
3. Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement (Asidan).
Ikeda Y; Ohta Y; Kobayashi H; Okamoto M; Takamatsu K; Ota T; Manabe Y; Okamoto K; Koizumi A; Abe K
Neurology; 2012 Jul; 79(4):333-41. PubMed ID: 22744658
[TBL] [Abstract][Full Text] [Related]
4. [Spinocerebellar ataxia type 36 (nicknamed Asidan)].
Abe K; Ikeda Y
Brain Nerve; 2012 Aug; 64(8):937-41. PubMed ID: 22868885
[TBL] [Abstract][Full Text] [Related]
5. 'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization.
García-Murias M; Quintáns B; Arias M; Seixas AI; Cacheiro P; Tarrío R; Pardo J; Millán MJ; Arias-Rivas S; Blanco-Arias P; Dapena D; Moreira R; Rodríguez-Trelles F; Sequeiros J; Carracedo A; Silveira I; Sobrido MJ
Brain; 2012 May; 135(Pt 5):1423-35. PubMed ID: 22492559
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China.
Zeng S; Zeng J; He M; Zeng X; Zhou Y; Liu Z; Xia K; Pan Q; Jiang H; Shen L; Yan X; Tang B; Wang J
Clin Genet; 2016 Aug; 90(2):141-8. PubMed ID: 26661328
[TBL] [Abstract][Full Text] [Related]
8. Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes.
Aydin G; Dekomien G; Hoffjan S; Gerding WM; Epplen JT; Arning L
BMC Neurol; 2018 Jan; 18(1):3. PubMed ID: 29316893
[TBL] [Abstract][Full Text] [Related]
9. Porphyrins ameliorate spinocerebellar ataxia type 36 GGCCTG repeat expansion-mediated cytotoxicity.
Hirayanagi K; Ozaki H; Tsukagoshi S; Furuta N; Ikeda Y
Neurosci Res; 2021 Oct; 171():92-102. PubMed ID: 33705846
[TBL] [Abstract][Full Text] [Related]
10. [Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].
Zeng S; Tang B; Wang J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):886-9. PubMed ID: 26663071
[TBL] [Abstract][Full Text] [Related]
11. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
[TBL] [Abstract][Full Text] [Related]
12. Long-read sequencing identified intronic (GGCCTG)n expansion in NOP56 in one SCA36 family and literature review.
Wang Q; Zhang C; Liu S; Liu T; Ni R; Liu X; Zhong P; Wu Q; Xu T; Ke H; Tian W; Cao L
Clin Neurol Neurosurg; 2022 Dec; 223():107503. PubMed ID: 36368168
[TBL] [Abstract][Full Text] [Related]
13. Spinocerebellar ataxia type 36 in the Han Chinese.
Lee YC; Tsai PC; Guo YC; Hsiao CT; Liu GT; Liao YC; Soong BW
Neurol Genet; 2016 Jun; 2(3):e68. PubMed ID: 27123487
[TBL] [Abstract][Full Text] [Related]
14. A Chinese SCA36 pedigree analysis of
Zou J; Wang F; Gong Z; Wang R; Chen S; Zhang H; Sun R; Gao C; Li W; Shang J; Zhang J
Front Genet; 2023; 14():1110307. PubMed ID: 37051597
[No Abstract] [Full Text] [Related]
15. Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.
Ikeda Y; Dalton JC; Moseley ML; Gardner KL; Bird TD; Ashizawa T; Seltzer WK; Pandolfo M; Milunsky A; Potter NT; Shoji M; Vincent JB; Day JW; Ranum LP
Am J Hum Genet; 2004 Jul; 75(1):3-16. PubMed ID: 15152344
[TBL] [Abstract][Full Text] [Related]
16. Repeat expansions in
Lam T; Rocca C; Ibanez K; Dalmia A; Tallman S; Hadjivassiliou M; Hensiek A; Nemeth A; Facchini S; ; Wood N; Cortese A; Houlden H; Tucci A
Brain Commun; 2023; 5(5):fcad244. PubMed ID: 37810464
[TBL] [Abstract][Full Text] [Related]
17. Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
Silveira I; Miranda C; Guimarães L; Moreira MC; Alonso I; Mendonça P; Ferro A; Pinto-Basto J; Coelho J; Ferreirinha F; Poirier J; Parreira E; Vale J; Januário C; Barbot C; Tuna A; Barros J; Koide R; Tsuji S; Holmes SE; Margolis RL; Jardim L; Pandolfo M; Coutinho P; Sequeiros J
Arch Neurol; 2002 Apr; 59(4):623-9. PubMed ID: 11939898
[TBL] [Abstract][Full Text] [Related]
18. Suppression of the yeast elongation factor Spt4 ortholog reduces expanded SCA36 GGCCUG repeat aggregation and cytotoxicity.
Furuta N; Tsukagoshi S; Hirayanagi K; Ikeda Y
Brain Res; 2019 May; 1711():29-40. PubMed ID: 30610877
[TBL] [Abstract][Full Text] [Related]
19. Analysis of a fully penetrant spinocerebellar ataxia type 8 Brazilian family.
Cintra VP; Lourenço CM; Rocha MMV; Tomaselli PJ; Marques W
Acta Neurol Scand; 2017 Nov; 136(5):541-545. PubMed ID: 28229454
[TBL] [Abstract][Full Text] [Related]
20. Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37.
Corral-Juan M; Serrano-Munuera C; Rábano A; Cota-González D; Segarra-Roca A; Ispierto L; Cano-Orgaz AT; Adarmes AD; Méndez-Del-Barrio C; Jesús S; Mir P; Volpini V; Alvarez-Ramo R; Sánchez I; Matilla-Dueñas A
Brain; 2018 Jul; 141(7):1981-1997. PubMed ID: 29939198
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
