BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 22082423)

  • 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; 51(10):1542-6. PubMed ID: 22082423
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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. PubMed ID: 19624685
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 18498393
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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. PubMed ID: 22136990
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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. PubMed ID: 21824570
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 75(11):967-72. PubMed ID: 20837964
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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. PubMed ID: 25266619
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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. PubMed ID: 11814735
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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. PubMed ID: 20974584
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 53(1):38-43. PubMed ID: 10408534
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
    Alonso I; Barros J; Tuna A; Coelho J; Sequeiros J; Silveira I; Coutinho P
    Arch Neurol; 2003 Apr; 60(4):610-4. PubMed ID: 12707077
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stepwise developmental regression associated with novel CACNA1A mutation.
    Guerin AA; Feigenbaum A; Donner EJ; Yoon G
    Pediatr Neurol; 2008 Nov; 39(5):363-4. PubMed ID: 18940563
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screen for CACNA1A and ATP1A2 mutations in sporadic hemiplegic migraine patients.
    Thomsen LL; Oestergaard E; Bjornsson A; Stefansson H; Fasquel AC; Gulcher J; Stefansson K; Olesen J
    Cephalalgia; 2008 Sep; 28(9):914-21. PubMed ID: 18513263
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Early-onset cerebellar atrophy associated with mutation in the CACNA1A gene.
    Naik S; Pohl K; Malik M; Siddiqui A; Josifova D
    Pediatr Neurol; 2011 Nov; 45(5):328-30. PubMed ID: 22000314
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The genetic spectrum of a population-based sample of familial hemiplegic migraine.
    Thomsen LL; Kirchmann M; Bjornsson A; Stefansson H; Jensen RM; Fasquel AC; Petursson H; Stefansson M; Frigge ML; Kong A; Gulcher J; Stefansson K; Olesen J
    Brain; 2007 Feb; 130(Pt 2):346-56. PubMed ID: 17142831
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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. PubMed ID: 11167897
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Familial hemiplegic migraine].
    Thomsen LL; Olesen J; Russell MB
    Ugeskr Laeger; 1998 Sep; 160(37):5325-9. PubMed ID: 9748855
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CACNA1A mutations: hemiplegic migraine, episodic ataxia type 2, and the others.
    Tournier-Lasserve E
    Neurology; 1999 Jul; 53(1):3-4. PubMed ID: 10408526
    [No Abstract]   [Full Text] [Related]  

  • 20. 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; 54(2):510-2. PubMed ID: 10668728
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.