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Results: 1 to 20 of 378

1.

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]
2.

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]
3.

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]
4.

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]
5.

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.

PMID:
12707077
[PubMed - indexed for MEDLINE]
6.

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]
7.

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. Epub 2006 Dec 2.

PMID:
17142831
[PubMed - indexed for MEDLINE]
Free Article
8.

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 8;105(8):707-12.

PMID:
11803518
[PubMed - indexed for MEDLINE]
9.

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.

PMID:
12111614
[PubMed - indexed for MEDLINE]
10.

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 1;22(1):21-6.

PMID:
7959770
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
9579893
[PubMed - indexed for MEDLINE]
12.

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
13.

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.

PMID:
9403481
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
12953268
[PubMed - indexed for MEDLINE]
15.

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.

Jones KW, Ehm MG, Pericak-Vance MA, Haines JL, Boyd PR, Peroutka SJ.

Genomics. 2001 Dec;78(3):150-4.

PMID:
11735221
[PubMed - indexed for MEDLINE]
16.

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.

Kaunisto MA, Harno H, Vanmolkot KR, Gargus JJ, Sun G, Hämäläinen E, Liukkonen E, Kallela M, van den Maagdenberg AM, Frants RR, Färkkilä M, Palotie A, Wessman M.

Neurogenetics. 2004 Jun;5(2):141-6. Epub 2004 May 7.

PMID:
15133718
[PubMed - indexed for MEDLINE]
17.

A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group.

Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Mohrenweiser H, Litt M, Hofker MH, Haan J, Ferrari MD, Frants RR.

Eur J Hum Genet. 1996;4(6):321-8.

PMID:
9043864
[PubMed - indexed for MEDLINE]
18.

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.

PMID:
9596000
[PubMed - indexed for MEDLINE]
19.

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. Review.

PMID:
9436352
[PubMed - indexed for MEDLINE]
20.

Genetic heterogeneity of familial hemiplegic migraine.

Joutel A, Ducros A, Vahedi K, Labauge P, Delrieu O, Pinsard N, Mancini J, Ponsot G, Gouttière F, Gastaut JL, et al.

Am J Hum Genet. 1994 Dec;55(6):1166-72.

PMID:
7977376
[PubMed - indexed for MEDLINE]
Free PMC Article

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