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Journal Abstract Search

173 related items for PubMed ID: 15775664

  • 1. [Familial hemiplegic migraine].
    Takahashi T, Igarashi S, Tsuji S.
    Clin Calcium; 2001 Nov; 11(11):1460-3. PubMed ID: 15775664
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
    Ducros A, Denier C, Joutel A, Cecillon M, Lescoat C, Vahedi K, Darcel F, Vicaut E, Bousser MG, Tournier-Lasserve E.
    N Engl J Med; 2001 Jul 05; 345(1):17-24. PubMed ID: 11439943
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  • 4. Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia.
    Veneziano L, Guida S, Mantuano E, Bernard P, Tarantino P, Boccone L, Hisama FM, Carrera P, Jodice C, Frontali M.
    J Neurol Sci; 2009 Jan 15; 276(1-2):31-7. PubMed ID: 18976783
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  • 5. 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 15; 130(Pt 2):346-56. PubMed ID: 17142831
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  • 6. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
    Tonelli A, D'Angelo MG, Salati R, Villa L, Germinasi C, Frattini T, Meola G, Turconi AC, Bresolin N, Bassi MT.
    J Neurol Sci; 2006 Feb 15; 241(1-2):13-7. PubMed ID: 16325861
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  • 8. [Molecular genetic findings in migraine].
    Østergaard E, Thomsen LL, Russell MB.
    Ugeskr Laeger; 2001 Nov 05; 163(45):6260-5. PubMed ID: 11723684
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  • 9. 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 Nov 05; 6(4):297-307. PubMed ID: 9781035
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  • 10. Familial hemiplegic migraine: involvement of a calcium neuronal channel.
    Ophoff RA, Terwindt GM, Vergouwe MN, Frants RR, Ferrari MD.
    Neurologia; 1997 Dec 05; 12 Suppl 5():31-7. PubMed ID: 9436352
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  • 11. 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 05; 54(3):360-6. PubMed ID: 12953268
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  • 12. 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 05; 50(4):1105-10. PubMed ID: 9566402
    [Abstract] [Full Text] [Related]

  • 13. [Familial hemiplegic migraine].
    Thomsen LL, Olesen J, Russell MB.
    Ugeskr Laeger; 1998 Sep 07; 160(37):5325-9. PubMed ID: 9748855
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  • 14. 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 07; 42(6):885-90. PubMed ID: 9403481
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  • 20. [Familial and sporadic hemiplegic migraine].
    Ducros A.
    Rev Neurol (Paris); 2008 Mar 07; 164(3):216-24. PubMed ID: 18405771
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