144 related articles for article (PubMed ID: 11355155)
1. Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?
Julien J; Denier C; Ferrer X; Ducros A; Saintarailles J; Lagueny A; Tournier-Lasserve E; Vital C
J Neurol; 2001 Mar; 248(3):209-14. PubMed ID: 11355155
[TBL] [Abstract][Full Text] [Related]
2. Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.
Cricchi F; Di Lorenzo C; Grieco GS; Rengo C; Cardinale A; Racaniello M; Santorelli FM; Nappi G; Pierelli F; Casali C
J Neurol Sci; 2007 Mar; 254(1-2):69-71. PubMed ID: 17292920
[TBL] [Abstract][Full Text] [Related]
3. Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.
Jodice C; Mantuano E; Veneziano L; Trettel F; Sabbadini G; Calandriello L; Francia A; Spadaro M; Pierelli F; Salvi F; Ophoff RA; Frants RR; Frontali M
Hum Mol Genet; 1997 Oct; 6(11):1973-8. PubMed ID: 9302278
[TBL] [Abstract][Full Text] [Related]
4. High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.
Denier C; Ducros A; Vahedi K; Joutel A; Thierry P; Ritz A; Castelnovo G; Deonna T; Gérard P; Devoize JL; Gayou A; Perrouty B; Soisson T; Autret A; Warter JM; Vighetto A; Van Bogaert P; Alamowitch S; Roullet E; Tournier-Lasserve E
Neurology; 1999 Jun; 52(9):1816-21. PubMed ID: 10371528
[TBL] [Abstract][Full Text] [Related]
5. Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia.
Jen JC; Yue Q; Karrim J; Nelson SF; Baloh RW
J Neurol Neurosurg Psychiatry; 1998 Oct; 65(4):565-8. PubMed ID: 9771787
[TBL] [Abstract][Full Text] [Related]
6. Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6.
Ishikawa K; Fujigasaki H; Saegusa H; Ohwada K; Fujita T; Iwamoto H; Komatsuzaki Y; Toru S; Toriyama H; Watanabe M; Ohkoshi N; Shoji S; Kanazawa I; Tanabe T; Mizusawa H
Hum Mol Genet; 1999 Jul; 8(7):1185-93. PubMed ID: 10369863
[TBL] [Abstract][Full Text] [Related]
7. Hereditary paroxysmal ataxia with mental retardation: a clinicopathological study in relation to episodic ataxia type 2.
Mochizuki Y; Kawata A; Mizutani T; Takamoto K; Hayashi H; Taki K; Morimatsu Y
Acta Neuropathol; 2004 Oct; 108(4):345-9. PubMed ID: 15300451
[TBL] [Abstract][Full Text] [Related]
8. Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6).
Sasaki H; Kojima H; Yabe I; Tashiro K; Hamada T; Sawa H; Hiraga H; Nagashima K
Acta Neuropathol; 1998 Feb; 95(2):199-204. PubMed ID: 9498057
[TBL] [Abstract][Full Text] [Related]
9. An autopsy case of spinocerebellar ataxia type 6 with mental symptoms of schizophrenia and dementia.
Tashiro H; Suzuki SO; Hitotsumatsu T; Iwaki T
Clin Neuropathol; 1999; 18(4):198-204. PubMed ID: 10442462
[TBL] [Abstract][Full Text] [Related]
10. Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia.
Spacey SD; Materek LA; Szczygielski BI; Bird TD
Arch Neurol; 2005 Feb; 62(2):314-6. PubMed ID: 15710862
[TBL] [Abstract][Full Text] [Related]
11. Late onset hereditary episodic ataxia.
Damak M; Riant F; Boukobza M; Tournier-Lasserve E; Bousser MG; Vahedi K
J Neurol Neurosurg Psychiatry; 2009 May; 80(5):566-8. PubMed ID: 19372292
[TBL] [Abstract][Full Text] [Related]
12. [Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)].
Ishikawa K; Mizusawa H
Nihon Rinsho; 1999 Apr; 57(4):880-5. PubMed ID: 10222783
[TBL] [Abstract][Full Text] [Related]
13. CACNA1A mutation in a EA-2 patient responsive to acetazolamide and valproic acid.
Scoggan KA; Friedman JH; Bulman DE
Can J Neurol Sci; 2006 Feb; 33(1):68-72. PubMed ID: 16583725
[TBL] [Abstract][Full Text] [Related]
14. Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6).
Ishikawa K; Watanabe M; Yoshizawa K; Fujita T; Iwamoto H; Yoshizawa T; Harada K; Nakamagoe K; Komatsuzaki Y; Satoh A; Doi M; Ogata T; Kanazawa I; Shoji S; Mizusawa H
J Neurol Neurosurg Psychiatry; 1999 Jul; 67(1):86-9. PubMed ID: 10369828
[TBL] [Abstract][Full Text] [Related]
15. Episodic ataxia type 2 (EA2) with interictal myokymia and focal dystonia.
Nielsen EN; Ásbjörnsdóttir B; Møller LB; Nielsen JE; Lindquist SG
Cold Spring Harb Mol Case Stud; 2022 Oct; 8(6):. PubMed ID: 36307210
[TBL] [Abstract][Full Text] [Related]
16. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
Schöls L; Krüger R; Amoiridis G; Przuntek H; Epplen JT; Riess O
J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):67-73. PubMed ID: 9436730
[TBL] [Abstract][Full Text] [Related]
17. Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
Gomez CM; Thompson RM; Gammack JT; Perlman SL; Dobyns WB; Truwit CL; Zee DS; Clark HB; Anderson JH
Ann Neurol; 1997 Dec; 42(6):933-50. PubMed ID: 9403487
[TBL] [Abstract][Full Text] [Related]
18. Missense CACNA1A mutation causing episodic ataxia type 2.
Denier C; Ducros A; Durr A; Eymard B; Chassande B; Tournier-Lasserve E
Arch Neurol; 2001 Feb; 58(2):292-5. PubMed ID: 11176968
[TBL] [Abstract][Full Text] [Related]
19. [Initial symptoms and mode of neurological progression in spinocerebellar ataxia type 6 (SCA6)].
Yabe I; Sasaki H; Yamashita I; Takei A; Fukazawa T; Hamada T; Tashiro K
Rinsho Shinkeigaku; 1998 Jun; 38(6):489-94. PubMed ID: 9847664
[TBL] [Abstract][Full Text] [Related]
20. Clinical and molecular genetic study in seven Japanese families with spinocerebellar ataxia type 6.
Nagai Y; Azuma T; Funauchi M; Fujita M; Umi M; Hirano M; Matsubara T; Ueno S
J Neurol Sci; 1998 Apr; 157(1):52-9. PubMed ID: 9600677
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]