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2. Calcium channel mutations and migraine. Kors EE; van den Maagdenberg AM; Plomp JJ; Frants RR; Ferrari MD Curr Opin Neurol; 2002 Jun; 15(3):311-6. PubMed ID: 12045730 [TBL] [Abstract][Full Text] [Related]
3. Calcium channels and channelopathies of the central nervous system. Pietrobon D Mol Neurobiol; 2002 Feb; 25(1):31-50. PubMed ID: 11890456 [TBL] [Abstract][Full Text] [Related]
4. The genetics of migraine: implication for treatment approaches. Ferrari MD; Haan J J Neural Transm Suppl; 2002; (63):111-27. PubMed ID: 12597612 [TBL] [Abstract][Full Text] [Related]
5. Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group. Terwindt GM; Ophoff RA; Haan J; Sandkuijl LA; Frants RR; Ferrari MD Eur J Hum Genet; 1998; 6(4):297-307. PubMed ID: 9781035 [TBL] [Abstract][Full Text] [Related]
6. Pathophysiological mechanisms of migraine and epilepsy: Similarities and differences. Mantegazza M; Cestèle S Neurosci Lett; 2018 Feb; 667():92-102. PubMed ID: 29129678 [TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 9566402 [TBL] [Abstract][Full Text] [Related]
8. The familial hemiplegic migraine type 1 mutation K1336E affects direct G protein-mediated regulation of neuronal P/Q-type Ca2+ channels. Garza-López E; González-Ramírez R; Gandini MA; Sandoval A; Felix R Cephalalgia; 2013 Apr; 33(6):398-407. PubMed ID: 23430985 [TBL] [Abstract][Full Text] [Related]
10. A review of the genetic relation between migraine and epilepsy. Haan J; Terwindt GM; van den Maagdenberg AM; Stam AH; Ferrari MD Cephalalgia; 2008 Feb; 28(2):105-13. PubMed ID: 18197881 [TBL] [Abstract][Full Text] [Related]
11. A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine. Alonso I; Barros J; Tuna A; Seixas A; Coutinho P; Sequeiros J; Silveira I Clin Genet; 2004 Jan; 65(1):70-2. PubMed ID: 15032980 [No Abstract] [Full Text] [Related]
12. Effects of familial hemiplegic migraine type 1 mutations on neuronal P/Q-type Ca2+ channel activity and inhibitory synaptic transmission. Cao YQ; Tsien RW Proc Natl Acad Sci U S A; 2005 Feb; 102(7):2590-5. PubMed ID: 15699344 [TBL] [Abstract][Full Text] [Related]
13. Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel. Jouvenceau A; Eunson LH; Spauschus A; Ramesh V; Zuberi SM; Kullmann DM; Hanna MG Lancet; 2001 Sep; 358(9284):801-7. PubMed ID: 11564488 [TBL] [Abstract][Full Text] [Related]
14. Mutant P/Q-type calcium channel electrophysiology and migraine. Plomp JJ; van den Maagdenberg AM; Molenaar PC; Frants RR; Ferrari MD Curr Opin Investig Drugs; 2001 Sep; 2(9):1250-60. PubMed ID: 11717812 [TBL] [Abstract][Full Text] [Related]
15. Genetics of migraine: possible links to neurophysiological abnormalities. Sándor PS; Ambrosini A; Agosti RM; Schoenen J Headache; 2002 May; 42(5):365-77. PubMed ID: 12047339 [No Abstract] [Full Text] [Related]
16. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Ophoff RA; Terwindt GM; Vergouwe MN; van Eijk R; Oefner PJ; Hoffman SM; Lamerdin JE; Mohrenweiser HW; Bulman DE; Ferrari M; Haan J; Lindhout D; van Ommen GJ; Hofker MH; Ferrari MD; Frants RR Cell; 1996 Nov; 87(3):543-52. PubMed ID: 8898206 [TBL] [Abstract][Full Text] [Related]
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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. [Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders]. Terwindt GM; Ophoff RA; Haan J; Frants RR; Ferrari MD Ned Tijdschr Geneeskd; 1998 May; 142(18):1015-9. PubMed ID: 9623202 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]