265 related articles for article (PubMed ID: 9579893)
1. Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.
Terwindt GM; Ophoff RA; Lindhout D; Haan J; Halley DJ; Sandkuijl LA; Brouwer OF; Frants RR; Ferrari MD
Epilepsia; 1997 Aug; 38(8):915-21. PubMed ID: 9579893
[TBL] [Abstract][Full Text] [Related]
2. 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; 53(1):26-33. PubMed ID: 10408532
[TBL] [Abstract][Full Text] [Related]
3. Genetic heterogeneity of familial hemiplegic migraine.
Ophoff RA; van Eijk R; Sandkuijl LA; Terwindt GM; Grubben CP; Haan J; Lindhout D; Ferrari MD; Frants RR
Genomics; 1994 Jul; 22(1):21-6. PubMed ID: 7959770
[TBL] [Abstract][Full Text] [Related]
4. Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q.
Steinlein O; Schuster V; Fischer C; Häussler M
Hum Genet; 1995 Apr; 95(4):411-5. PubMed ID: 7705837
[TBL] [Abstract][Full Text] [Related]
5. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.
Ducros A; Joutel A; Vahedi K; Cecillon M; Ferreira A; Bernard E; Verier A; Echenne B; Lopez de Munain A; Bousser MG; Tournier-Lasserve E
Ann Neurol; 1997 Dec; 42(6):885-90. PubMed ID: 9403481
[TBL] [Abstract][Full Text] [Related]
6. Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.
Nyholt DR; Lea RA; Goadsby PJ; Brimage PJ; Griffiths LR
Neurology; 1998 May; 50(5):1428-32. PubMed ID: 9596000
[TBL] [Abstract][Full Text] [Related]
7. Evidence of a third locus for benign familial convulsions.
Lewis TB; Shevell MI; Andermann E; Ryan SG; Leach RJ
J Child Neurol; 1996 May; 11(3):211-4. PubMed ID: 8734025
[TBL] [Abstract][Full Text] [Related]
8. Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG.
Terwindt GM; Ophoff RA; Haan J; Frants RR; Ferrari MD
Cephalalgia; 1996 May; 16(3):153-5. PubMed ID: 8734765
[TBL] [Abstract][Full Text] [Related]
9. Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Vanmolkot KR; Kors EE; Hottenga JJ; Terwindt GM; Haan J; Hoefnagels WA; Black DF; Sandkuijl LA; Frants RR; Ferrari MD; van den Maagdenberg AM
Ann Neurol; 2003 Sep; 54(3):360-6. PubMed ID: 12953268
[TBL] [Abstract][Full Text] [Related]
10. A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.
Münchau A; Valente EM; Shahidi GA; Eunson LH; Hanna MG; Quinn NP; Schapira AH; Wood NW; Bhatia KP
J Neurol Neurosurg Psychiatry; 2000 May; 68(5):609-14. PubMed ID: 10766892
[TBL] [Abstract][Full Text] [Related]
11. Familial hemiplegic migraine: involvement of a calcium neuronal channel.
Ophoff RA; Terwindt GM; Vergouwe MN; Frants RR; Ferrari MD
Neurologia; 1997 Dec; 12 Suppl 5():31-7. PubMed ID: 9436352
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. 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]
14. 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]
15. Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility.
Lea RA; Curtain RP; Hutchins C; Brimage PJ; Griffiths LR
Am J Med Genet; 2001 Dec; 105(8):707-12. PubMed ID: 11803518
[TBL] [Abstract][Full Text] [Related]
16. Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q.
Guipponi M; Rivier F; Vigevano F; Beck C; Crespel A; Echenne B; Lucchini P; Sebastianelli R; Baldy-Moulinier M; Malafosse A
Hum Mol Genet; 1997 Mar; 6(3):473-7. PubMed ID: 9147652
[TBL] [Abstract][Full Text] [Related]
17. Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions.
Neubauer BA; Moises HW; Lässker U; Waltz S; Diebold U; Stephani U
Epilepsia; 1997 Jul; 38(7):782-7. PubMed ID: 9579905
[TBL] [Abstract][Full Text] [Related]
18. Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.
Cevoli S; Pierangeli G; Monari L; Valentino ML; Bernardoni P; Mochi M; Cortelli P; Montagna P
Neurol Sci; 2002 Apr; 23(1):7-10. PubMed ID: 12111614
[TBL] [Abstract][Full Text] [Related]
19. Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.
Caraballo R; Pavek S; Lemainque A; Gastaldi M; Echenne B; Motte J; Genton P; Cersósimo R; Humbertclaude V; Fejerman N; Monaco AP; Lathrop MG; Rochette J; Szepetowski P
Am J Hum Genet; 2001 Mar; 68(3):788-94. PubMed ID: 11179027
[TBL] [Abstract][Full Text] [Related]
20. Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q.
Lewis TB; Leach RJ; Ward K; O'Connell P; Ryan SG
Am J Hum Genet; 1993 Sep; 53(3):670-5. PubMed ID: 8102508
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]