Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 129

1.

Acetazolamide-responsive ataxia.

Kotagal V.

Semin Neurol. 2012 Nov;32(5):533-7. doi: 10.1055/s-0033-1334475. Epub 2013 May 15. Review.

PMID:
23677664
2.

Familial episodic ataxia type II.

Mugundhan K, Thiruvarutchelvan K, Sivakumar S.

J Assoc Physicians India. 2011 Oct;59:668-70.

PMID:
22479753
3.

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. doi: 10.1136/jnnp.2008.150615.

PMID:
19372292
4.

[Hereditary episodic ataxia].

Riant F, Vahedi K, Tournier-Lasserve E.

Rev Neurol (Paris). 2011 May;167(5):401-7. doi: 10.1016/j.neurol.2010.10.016. Epub 2011 Apr 13. Review. French.

PMID:
21492892
5.

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 15;254(1-2):69-71. Epub 2007 Feb 12.

PMID:
17292920
6.

Clinical spectrum of episodic ataxia type 2.

Jen J, Kim GW, Baloh RW.

Neurology. 2004 Jan 13;62(1):17-22.

PMID:
14718690
7.

Aggravation of ataxia due to acetazolamide induced hyperammonaemia in episodic ataxia.

Kim JM, Ryu WS, Hwang YH, Kim JS.

J Neurol Neurosurg Psychiatry. 2007 Jul;78(7):771-2. No abstract available.

8.

Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine.

Kinder S, Ossig C, Wienecke M, Beyer A, von der Hagen M, Storch A, Smitka M.

Eur J Paediatr Neurol. 2015 Jan;19(1):72-4. doi: 10.1016/j.ejpn.2014.10.005. Epub 2014 Nov 3.

PMID:
25468264
9.

Fluctuating neuromuscular transmission defects and inverse acetazolamide response in episodic ataxia type 2 associated with the novel CaV2.1 single amino acid substitution R2090Q.

Melzer N, Classen J, Reiners K, Buttmann M.

J Neurol Sci. 2010 Sep 15;296(1-2):104-6. doi: 10.1016/j.jns.2010.06.024.

PMID:
20663518
10.

De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia.

Yue Q, Jen JC, Thwe MM, Nelson SF, Baloh RW.

Am J Med Genet. 1998 May 26;77(4):298-301.

PMID:
9600739
11.

Acetazolamide-responsive episodic ataxia syndrome.

Zasorin NL, Baloh RW, Myers LB.

Neurology. 1983 Sep;33(9):1212-4.

PMID:
6684259
12.

[Familial episodic ataxia type 2. Clinical and genetic study of one family].

Suárez-Cuervo A, Salas-Puig J, Alvarez V, Coto E, Fernández JM, Lahoz CH.

Neurologia. 1998 Oct;13(8):382-7. Spanish.

PMID:
9859670
13.

Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine.

Strupp M, Kalla R, Dichgans M, Freilinger T, Glasauer S, Brandt T.

Neurology. 2004 May 11;62(9):1623-5.

PMID:
15136697
14.

[Familial paroxysmal ataxia responsive to acetazolamide].

Aimard G, Vighetto A, Trillet M, Ventre JJ, Devic M.

Rev Neurol (Paris). 1983;139(4):251-8. French.

PMID:
6612140
15.

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.

PMID:
16583725
16.

Episodic ataxia and channelopathies.

Gordon N.

Brain Dev. 1998 Jan;20(1):9-13. Review.

PMID:
9533553
17.

Use of acetazolamide in sulfonamide-allergic patients with neurologic channelopathies.

Platt D, Griggs RC.

Arch Neurol. 2012 Apr;69(4):527-9. doi: 10.1001/archneurol.2011.2723. Epub 2011 Dec 12.

18.

[Familial paroxysmal ataxia: a new case].

Escribano JB, Moltó JM, Martínez-García FA, Morales A, Jiménez-Martínez JM, Fernández-Barreiro A.

Rev Neurol. 1996 May;24(129):567-9. Spanish.

PMID:
8681176
19.

[Episodic ataxia without myokymia].

Yabe I, Sasaki H.

Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):322-5. Review. Japanese. No abstract available.

PMID:
12483892
20.

Familial periodic ataxia responsive to acetazolamide.

Bouchard JP, Roberge C, van Gelder NM, Barbeau A.

Can J Neurol Sci. 1984 Nov;11(4 Suppl):550-3.

PMID:
6439406

Supplemental Content

Support Center