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Results: 1 to 20 of 112

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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
4.

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
[PubMed - indexed for MEDLINE]
5.

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
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

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
[PubMed - indexed for MEDLINE]
10.

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
[PubMed - indexed for MEDLINE]
11.

Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene.

Haan J, Kors EE, Terwindt GM, Vermeulen FL, Vergouwe MN, van den Maagdenberg AM, Gill DS, Pascual J, Ophoff RA, Frants RR, Ferrari.

Cephalalgia. 2000 Oct;20(8):696-700.

PMID:
11167897
[PubMed - indexed for MEDLINE]
12.

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
[PubMed - indexed for MEDLINE]
13.

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
[PubMed - indexed for MEDLINE]
14.

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.

Kors EE, Haan J, Giffin NJ, Pazdera L, Schnittger C, Lennox GG, Terwindt GM, Vermeulen FL, Van den Maagdenberg AM, Frants RR, Ferrari MD.

Arch Neurol. 2003 May;60(5):684-8.

PMID:
12756131
[PubMed - indexed for MEDLINE]
15.

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.

PMID:
9915947
[PubMed - indexed for MEDLINE]
Free PMC Article
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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.

PMID:
11971066
[PubMed - indexed for MEDLINE]
Free PMC Article
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
[PubMed - indexed for MEDLINE]
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