These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 12849225)

  • 1. Second gene identified for familial hemiplegic migraine.
    Bradbury J
    Lancet Neurol; 2003 Mar; 2(3):137. PubMed ID: 12849225
    [No Abstract]   [Full Text] [Related]  

  • 2. [From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene].
    Kors EE; Vanmolkot KR; Haan J; van den Maagdenberg AM; Frants RR; Ferrari MD
    Ned Tijdschr Geneeskd; 2004 Sep; 148(39):1919-20. PubMed ID: 15495990
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recent findings in headache genetics.
    Kors EE; Vanmolkot KR; Haan J; Frants RR; van den Maagdenberg AM; Ferrari MD
    Curr Opin Neurol; 2004 Jun; 17(3):283-8. PubMed ID: 15167062
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
    Fernandez DM; Hand CK; Sweeney BJ; Parfrey NA
    Headache; 2008 Jan; 48(1):101-8. PubMed ID: 18184292
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
    Ambrosini A; D'Onofrio M; Grieco GS; Di Mambro A; Montagna G; Fortini D; Nicoletti F; Nappi G; Sances G; Schoenen J; Buzzi MG; Santorelli FM; Pierelli F
    Neurology; 2005 Dec; 65(11):1826-8. PubMed ID: 16344534
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Calcium channels and migraine].
    Couraud F; Seagar M
    Pathol Biol (Paris); 2000 Sep; 48(7):642-7. PubMed ID: 11072642
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation.
    De Sanctis S; Grieco GS; Breda L; Casali C; Nozzi M; Del Torto M; Chiarelli F; Verrotti A
    Headache; 2011 Mar; 51(3):447-450. PubMed ID: 21352219
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular genetics of migraine.
    de Vries B; Frants RR; Ferrari MD; van den Maagdenberg AM
    Hum Genet; 2009 Jul; 126(1):115-32. PubMed ID: 19455354
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes.
    Moskowitz MA; Bolay H; Dalkara T
    Ann Neurol; 2004 Feb; 55(2):276-80. PubMed ID: 14755732
    [No Abstract]   [Full Text] [Related]  

  • 10. [From gene to disease; from CACNA1A to migraine].
    Kors EE; Haan J; Frants RR; Ferrari MD
    Ned Tijdschr Geneeskd; 2001 Feb; 145(6):266-7. PubMed ID: 11236374
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Single-fiber EMG in familial hemiplegic migraine.
    Terwindt GM; Kors EE; Vein AA; Ferrari MD; van Dijk JG
    Neurology; 2004 Nov; 63(10):1942-3. PubMed ID: 15557518
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.
    Lebas A; Guyant-Maréchal L; Hannequin D; Riant F; Tournier-Lasserve E; Parain D
    Cephalalgia; 2008 Jul; 28(7):774-7. PubMed ID: 18498390
    [TBL] [Abstract][Full Text] [Related]  

  • 13. FHM3 in familial hemiplegic migraine is more resistant to mutation than FHM1 and FHM2.
    Wiwanitkit V
    J Neurol Sci; 2009 Feb; 277(1-2):76-9. PubMed ID: 19007941
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genetics of migraine].
    Ducros A
    Pathol Biol (Paris); 2000 Sep; 48(7):658-62. PubMed ID: 11072644
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
    De Fusco M; Marconi R; Silvestri L; Atorino L; Rampoldi L; Morgante L; Ballabio A; Aridon P; Casari G
    Nat Genet; 2003 Feb; 33(2):192-6. PubMed ID: 12539047
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sporadic hemiplegic migraine in children.
    Pienczk-Reclawowicz K; Pilarska E; Lemka M
    Neurol India; 2010; 58(4):512-3. PubMed ID: 20739784
    [No Abstract]   [Full Text] [Related]  

  • 17. [Genetics of migraine].
    Freilinger T; Dichgans M
    Nervenarzt; 2006 Oct; 77(10):1186, 1188-95. PubMed ID: 16915377
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group.
    Ophoff RA; Terwindt GM; Vergouwe MN; Frants RR; Ferrari MD
    Headache; 1997 Sep; 37(8):479-85. PubMed ID: 9329229
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Is the CACNA1A gene involved in familial migraine with aura?
    Brugnoni R; Leone M; Rigamonti A; Moranduzzo E; Cornelio F; Mantegazza R; Bussone G
    Neurol Sci; 2002 Apr; 23(1):1-5. PubMed ID: 12111613
    [TBL] [Abstract][Full Text] [Related]  

  • 20. No mutations in CACNA1A and ATP1A2 in probands with common types of migraine.
    Jen JC; Kim GW; Dudding KA; Baloh RW
    Arch Neurol; 2004 Jun; 61(6):926-8. PubMed ID: 15210532
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.