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Journal Abstract Search

159 related items for PubMed ID: 9043864

  • 21. 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; 28(8):887-91. PubMed ID: 18498393
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  • 24. Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine.
    Dichgans M, Mayer M, Müller-Myhsok B, Straube A, Gasser T.
    Genomics; 1996 Feb 15; 32(1):151-4. PubMed ID: 8786108
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  • 25. 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 15; 23(1):7-10. PubMed ID: 12111614
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  • 26. [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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  • 27. 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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  • 31. 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 05; 37(8):479-85. PubMed ID: 9329229
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  • 32. 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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  • 36. Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG.
    Norberg A, Forsgren L, Holmberg D, Holmberg M.
    Neurosci Lett; 2006 Mar 27; 396(2):137-42. PubMed ID: 16378686
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  • 40. Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease.
    Li A, Davila S, Furu L, Qian Q, Tian X, Kamath PS, King BF, Torres VE, Somlo S.
    Am J Hum Genet; 2003 Mar 27; 72(3):691-703. PubMed ID: 12529853
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