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Journal Abstract Search

606 related items for PubMed ID: 12707077

  • 1. 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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  • 2. 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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  • 4. CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood.
    de Vries B, Stam AH, Beker F, van den Maagdenberg AM, Vanmolkot KR, Laan L, Ginjaar IB, Frants RR, Lauffer H, Haan J, Haas JP, Terwindt GM, Ferrari MD.
    Cephalalgia; 2008 Aug 15; 28(8):887-91. PubMed ID: 18498393
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  • 6. 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 15; 50(4):1105-10. PubMed ID: 9566402
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  • 10. [Familial hemiplegic migraine].
    Takahashi T, Igarashi S, Tsuji S.
    Clin Calcium; 2001 Nov 15; 11(11):1460-3. PubMed ID: 15775664
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  • 11. Familial hemiplegic migraine: involvement of a calcium neuronal channel.
    Ophoff RA, Terwindt GM, Vergouwe MN, Frants RR, Ferrari MD.
    Neurologia; 1997 Dec 15; 12 Suppl 5():31-7. PubMed ID: 9436352
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  • 14. [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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  • 20. Large CACNA1A deletion in a family with episodic ataxia type 2.
    Riant F, Mourtada R, Saugier-Veber P, Tournier-Lasserve E.
    Arch Neurol; 2008 Jun 05; 65(6):817-20. PubMed ID: 18541804
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