392 related articles for article (PubMed ID: 21827913)
1. Spinocerebellar ataxia 13 and 25.
Stevanin G; Dürr A
Handb Clin Neurol; 2012; 103():549-53. PubMed ID: 21827913
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Spinocerebellar ataxia with sensory neuropathy (SCA25).
Stevanin G; Broussolle E; Streichenberger N; Kopp N; Brice A; Durr A
Cerebellum; 2005; 4(1):58-61. PubMed ID: 15895562
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
Wolf NI; Koenig M
Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
[TBL] [Abstract][Full Text] [Related]
6. A Novel Pathogenic Variant in the SCA25-Related Gene Expanding the Etiology of Early-Onset and Progressive Cerebellar Ataxia in Childhood.
Ferrera G; Izzo R; Ghezzi D; Nanetti L; Lamantea E; Ardissone A
Neuropediatrics; 2024 Apr; 55(2):135-139. PubMed ID: 37935417
[TBL] [Abstract][Full Text] [Related]
7. TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment.
Delplanque J; Devos D; Huin V; Genet A; Sand O; Moreau C; Goizet C; Charles P; Anheim M; Monin ML; Buée L; Destée A; Grolez G; Delmaire C; Dujardin K; Dellacherie D; Brice A; Stevanin G; Strubi-Vuillaume I; Dürr A; Sablonnière B
Brain; 2014 Oct; 137(Pt 10):2657-63. PubMed ID: 25070513
[TBL] [Abstract][Full Text] [Related]
8. Evidence for a new spinocerebellar ataxia locus.
Higgins JJ; Pho LT; Ide SE; Nee LE; Polymeropoulos MH
Mov Disord; 1997 May; 12(3):412-7. PubMed ID: 9159738
[TBL] [Abstract][Full Text] [Related]
9. Spinocerebellar ataxia type 31 exists in northeast China.
Ouyang Y; He Z; Li L; Qin X; Zhao Y; Yuan L
J Neurol Sci; 2012 May; 316(1-2):164-7. PubMed ID: 22353852
[TBL] [Abstract][Full Text] [Related]
10. New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.
Klebe S; Durr A; Rentschler A; Hahn-Barma V; Abele M; Bouslam N; Schöls L; Jedynak P; Forlani S; Denis E; Dussert C; Agid Y; Bauer P; Globas C; Wüllner U; Brice A; Riess O; Stevanin G
Ann Neurol; 2005 Nov; 58(5):720-9. PubMed ID: 16193476
[TBL] [Abstract][Full Text] [Related]
11. Spinocerebellar ataxia with mental retardation (SCA13).
Stevanin G; Durr A; Benammar N; Brice A
Cerebellum; 2005; 4(1):43-6. PubMed ID: 15895558
[TBL] [Abstract][Full Text] [Related]
12. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
Yu GY; Howell MJ; Roller MJ; Xie TD; Gomez CM
Ann Neurol; 2005 Mar; 57(3):349-54. PubMed ID: 15732118
[TBL] [Abstract][Full Text] [Related]
13. Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
El Euch-Fayache G; Lalani I; Amouri R; Turki I; Ouahchi K; Hung WY; Belal S; Siddique T; Hentati F
Arch Neurol; 2003 Jul; 60(7):982-8. PubMed ID: 12873855
[TBL] [Abstract][Full Text] [Related]
14. Rare forms of autosomal recessive neurodegenerative ataxia.
Koenig M
Semin Pediatr Neurol; 2003 Sep; 10(3):183-92. PubMed ID: 14653406
[TBL] [Abstract][Full Text] [Related]
15. Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxias.
Nikali K; Koskinen T; Suomalainen A; Pihko H; Peltonen L
Pediatr Res; 1994 Nov; 36(5):607-12. PubMed ID: 7877879
[TBL] [Abstract][Full Text] [Related]
16. Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
Hiramoto K; Kawakami H; Inoue K; Seki T; Maruyama H; Morino H; Matsumoto M; Kurisu K; Sakai N
Mov Disord; 2006 Sep; 21(9):1355-60. PubMed ID: 16763984
[TBL] [Abstract][Full Text] [Related]
17. Spinocerebellar ataxia type 28.
Mariotti C; Bella DD; Di Donato S; Taroni F
Handb Clin Neurol; 2012; 103():575-9. PubMed ID: 21827917
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia.
Tada Y; Kume K; Matsuda Y; Kurashige T; Kanaya Y; Ohsawa R; Morino H; Tabu H; Kaneko S; Suenaga T; Kakizuka A; Kawakami H
J Hum Genet; 2020 Apr; 65(4):363-369. PubMed ID: 31907387
[TBL] [Abstract][Full Text] [Related]
20. KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking.
Gallego-Iradi C; Bickford JS; Khare S; Hall A; Nick JA; Salmasinia D; Wawrowsky K; Bannykh S; Huynh DP; Rincon-Limas DE; Pulst SM; Nick HS; Fernandez-Funez P; Waters MF
Neurobiol Dis; 2014 Nov; 71():270-9. PubMed ID: 25152487
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]