237 related articles for article (PubMed ID: 9390841)
1. Episodic ataxia type 1 and 2 (familial periodic ataxia/vertigo).
Brandt T; Strupp M
Audiol Neurootol; 1997; 2(6):373-83. PubMed ID: 9390841
[TBL] [Abstract][Full Text] [Related]
2. Genetics of familial episodic vertigo and ataxia.
Baloh RW; Jen JC
Ann N Y Acad Sci; 2002 Apr; 956():338-45. PubMed ID: 11960817
[TBL] [Abstract][Full Text] [Related]
3. [A sporadic case of episodic ataxia with nystagmus (EA-2)].
Namekawa M; Takiyama Y; Ueno N; Nishizawa M
Rinsho Shinkeigaku; 1998 May; 38(5):446-9. PubMed ID: 9805992
[TBL] [Abstract][Full Text] [Related]
4. [Episodic ataxias].
Herrmann A; Braathen GJ; Russell MB
Tidsskr Nor Laegeforen; 2005 Aug; 125(15):2005-7. PubMed ID: 16100538
[TBL] [Abstract][Full Text] [Related]
5. Episodic ataxia and channelopathies.
Gordon N
Brain Dev; 1998 Jan; 20(1):9-13. PubMed ID: 9533553
[TBL] [Abstract][Full Text] [Related]
6. [Familial periodic ataxia with myokymia sensitive to acetazolamide: a family case].
Gómez-Gosálvez F; Smeyers P; Escrivá P; Clemente F; Mallada J; Mulas F; Palao F; Millet E
Rev Neurol; 1997 Dec; 25(148):1925-7. PubMed ID: 9528033
[TBL] [Abstract][Full Text] [Related]
7. [Hereditary episodic ataxia].
Riant F; Vahedi K; Tournier-Lasserve E
Rev Neurol (Paris); 2011 May; 167(5):401-7. PubMed ID: 21492892
[TBL] [Abstract][Full Text] [Related]
8. Episodic ataxia type 2.
Strupp M; Zwergal A; Brandt T
Neurotherapeutics; 2007 Apr; 4(2):267-73. PubMed ID: 17395137
[TBL] [Abstract][Full Text] [Related]
9. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.
Browne DL; Gancher ST; Nutt JG; Brunt ER; Smith EA; Kramer P; Litt M
Nat Genet; 1994 Oct; 8(2):136-40. PubMed ID: 7842011
[TBL] [Abstract][Full Text] [Related]
10. Three novel KCNA1 mutations in episodic ataxia type I families.
Scheffer H; Brunt ER; Mol GJ; van der Vlies P; Stulp RP; Verlind E; Mantel G; Averyanov YN; Hofstra RM; Buys CH
Hum Genet; 1998 Apr; 102(4):464-6. PubMed ID: 9600245
[TBL] [Abstract][Full Text] [Related]
11. The efficacy of combining topiramate and 4-aminopyridine to reduce relapses and interictal progression in two cases of episodic ataxia type 2.
González-Mingot C; López-Ortega R; Brieva-Ruiz L
Neurol Sci; 2022 Aug; 43(8):5099-5101. PubMed ID: 35595874
[TBL] [Abstract][Full Text] [Related]
12. Novel splice site CACNA1A mutation causing episodic ataxia type 2.
Kaunisto MA; Harno H; Kallela M; Somer H; Sallinen R; Hämäläinen E; Miettinen PJ; Vesa J; Orpana A; Palotie A; Färkkilä M; Wessman M
Neurogenetics; 2004 Feb; 5(1):69-73. PubMed ID: 14530926
[TBL] [Abstract][Full Text] [Related]
13. Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13.
Teh BT; Silburn P; Lindblad K; Betz R; Boyle R; Schalling M; Larsson C
Am J Hum Genet; 1995 Jun; 56(6):1443-9. PubMed ID: 7762567
[TBL] [Abstract][Full Text] [Related]
14. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
Ophoff RA; Terwindt GM; Vergouwe MN; van Eijk R; Oefner PJ; Hoffman SM; Lamerdin JE; Mohrenweiser HW; Bulman DE; Ferrari M; Haan J; Lindhout D; van Ommen GJ; Hofker MH; Ferrari MD; Frants RR
Cell; 1996 Nov; 87(3):543-52. PubMed ID: 8898206
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Episodic ataxia and myokymia syndrome: a new mutation of potassium channel gene Kv1.1.
Comu S; Giuliani M; Narayanan V
Ann Neurol; 1996 Oct; 40(4):684-7. PubMed ID: 8871592
[TBL] [Abstract][Full Text] [Related]
17. Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamide.
Lubbers WJ; Brunt ER; Scheffer H; Litt M; Stulp R; Browne DL; van Weerden TW
J Neurol Neurosurg Psychiatry; 1995 Oct; 59(4):400-5. PubMed ID: 7561920
[TBL] [Abstract][Full Text] [Related]
18. Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K(+) channel function.
D'Adamo MC; Imbrici P; Sponcichetti F; Pessia M
FASEB J; 1999 Aug; 13(11):1335-45. PubMed ID: 10428758
[TBL] [Abstract][Full Text] [Related]
19. Episodic ataxia results from voltage-dependent potassium channels with altered functions.
Adelman JP; Bond CT; Pessia M; Maylie J
Neuron; 1995 Dec; 15(6):1449-54. PubMed ID: 8845167
[TBL] [Abstract][Full Text] [Related]
20. Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A.
García Segarra N; Gautschi I; Mittaz-Crettol L; Kallay Zetchi C; Al-Qusairi L; Van Bemmelen MX; Maeder P; Bonafé L; Schild L; Roulet-Perez E
J Neurol Sci; 2014 Jul; 342(1-2):69-78. PubMed ID: 24836863
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]