Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 128

1.

Acute striatal necrosis in hemiplegic migraine with de novo CACNA1A mutation.

Carreño O, García-Silva MT, García-Campos Ó, Martínez-de Aragón A, Cormand B, Macaya A.

Headache. 2011 Nov-Dec;51(10):1542-6. doi: 10.1111/j.1526-4610.2011.02014.x.

PMID:
22082423
2.

Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia.

Wada T, Kobayashi N, Takahashi Y, Aoki T, Watanabe T, Saitoh S.

Pediatr Neurol. 2002 Jan;26(1):47-50.

PMID:
11814735
3.

Link between confusional migraine, hemiplegic migraine and episodic ataxia type 2: hypothesis, family genealogy, gene typing and classification.

Cleves C, Parikh S, Rothner AD, Tepper SJ.

Cephalalgia. 2010 Jun;30(6):740-3. doi: 10.1111/j.1468-2982.2009.01958.x. Epub 2010 Feb 1.

PMID:
19624685
4.

CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood.

de Vries B, Stam AH, Beker F, van den Maagdenberg AM, Vanmolkot KR, Laan L, Ginjaar IB, Frants RR, Lauffer H, Haan J, Haas JP, Terwindt GM, Ferrari MD.

Cephalalgia. 2008 Aug;28(8):887-91. doi: 10.1111/j.1468-2982.2008.01596.x. Epub 2008 May 21.

PMID:
18498393
5.

Sporadic hemiplegic migraine presenting as acute encephalopathy.

Ohmura K, Suzuki Y, Saito Y, Wada T, Goto M, Seto S.

Brain Dev. 2012 Sep;34(8):691-5. doi: 10.1016/j.braindev.2011.11.002. Epub 2011 Dec 1.

PMID:
22136990
6.

Hemiconvulsion-hemiplegia-epilepsy syndrome associated with CACNA1A S218L mutation.

Yamazaki S, Ikeno K, Abe T, Tohyama J, Adachi Y.

Pediatr Neurol. 2011 Sep;45(3):193-6. doi: 10.1016/j.pediatrneurol.2011.04.010.

PMID:
21824570
7.

Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene.

Chabriat H, Vahedi K, Clark CA, Poupon C, Ducros A, Denier C, Le Bihan D, Bousser MG.

Neurology. 2000 Jan 25;54(2):510-2.

PMID:
10668728
8.

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.

Riant F, Ducros A, Ploton C, Barbance C, Depienne C, Tournier-Lasserve E.

Neurology. 2010 Sep 14;75(11):967-72. doi: 10.1212/WNL.0b013e3181f25e8f.

PMID:
20837964
9.

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

Terwindt GM, Ophoff RA, Haan J, Vergouwe MN, van Eijk R, Frants RR, Ferrari MD.

Neurology. 1998 Apr;50(4):1105-10.

PMID:
9566402
10.

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.

Vahedi K, Denier C, Ducros A, Bousson V, Levy C, Chabriat H, Haguenau M, Tournier-Lasserve E, Bousser MG.

Neurology. 2000 Oct 10;55(7):1040-2.

PMID:
11061267
11.

CACNA1A mutations: hemiplegic migraine, episodic ataxia type 2, and the others.

Tournier-Lasserve E.

Neurology. 1999 Jul 13;53(1):3-4. Review. No abstract available.

PMID:
10408526
12.

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia.

Battistini S, Stenirri S, Piatti M, Gelfi C, Righetti PG, Rocchi R, Giannini F, Battistini N, Guazzi GC, Ferrari M, Carrera P.

Neurology. 1999 Jul 13;53(1):38-43.

PMID:
10408534
13.

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 15;342(1-2):69-78. doi: 10.1016/j.jns.2014.04.027. Epub 2014 Apr 27.

PMID:
24836863
14.

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

Ducros A, Denier C, Joutel A, Vahedi K, Michel A, Darcel F, Madigand M, Guerouaou D, Tison F, Julien J, Hirsch E, Chedru F, Bisgård C, Lucotte G, Després P, Billard C, Barthez MA, Ponsot G, Bousser MG, Tournier-Lasserve E.

Am J Hum Genet. 1999 Jan;64(1):89-98.

15.

Phenotypic variability in a four generation family with a p.Thr666Met CACNA1A gene mutation.

García-Baró-Huarte M, Iglesias-Mohedano AM, Slöcker-Barrio M, Vázquez-López M, García-Morín M, Miranda-Herrero MC, Castro-Castro P.

Pediatr Neurol. 2014 Oct;51(4):557-9. doi: 10.1016/j.pediatrneurol.2014.07.008. Epub 2014 Jul 16.

PMID:
25266619
16.

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM.

Friend KL, Crimmins D, Phan TG, Sue CM, Colley A, Fung VS, Morris JG, Sutherland GR, Richards RI.

Hum Genet. 1999 Sep;105(3):261-5.

PMID:
10987655
17.

A long-term follow-up study of 18 patients with sporadic hemiplegic migraine.

Stam AH, Louter MA, Haan J, de Vries B, van den Maagdenberg AM, Frants RR, Ferrari MD, Terwindt GM.

Cephalalgia. 2011 Jan;31(2):199-205. doi: 10.1177/0333102410375629. Epub 2010 Jul 2.

PMID:
20974584
18.

Genetic heterogeneity in Italian families with familial hemiplegic migraine.

Carrera P, Piatti M, Stenirri S, Grimaldi LM, Marchioni E, Curcio M, Righetti PG, Ferrari M, Gelfi C.

Neurology. 1999 Jul 13;53(1):26-33.

PMID:
10408532
19.

Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene.

Takahashi T, Igarashi S, Kimura T, Hozumi I, Kawachi I, Onodera O, Takano H, Saito M, Tsuji S.

J Neurol Neurosurg Psychiatry. 2002 May;72(5):676-7. No abstract available.

20.

A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia.

Jen J, Yue Q, Nelson SF, Yu H, Litt M, Nutt J, Baloh RW.

Neurology. 1999 Jul 13;53(1):34-7.

PMID:
10408533

Supplemental Content

Support Center