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Journal Abstract Search

104 related items for PubMed ID: 15949411

  • 1. [Migraine and ion channels].
    Xu XP, Yang XD.
    Zhonghua Yi Xue Za Zhi; 2005 Mar 30; 85(12):859-61. PubMed ID: 15949411
    [No Abstract] [Full Text] [Related]

  • 2. Familial hemiplegic migraine: more than just a headache.
    Benatar M, Ford CC.
    Neurology; 2005 Feb 22; 64(4):592-3. PubMed ID: 15728276
    [No Abstract] [Full Text] [Related]

  • 3. Hemiplegic migraine--downstream of a single-base change.
    Hoffman EP.
    N Engl J Med; 2001 Jul 05; 345(1):57-9. PubMed ID: 11439951
    [No Abstract] [Full Text] [Related]

  • 4. Genetic models of migraine.
    van de Ven RC, Kaja S, Plomp JJ, Frants RR, van den Maagdenberg AM, Ferrari MD.
    Arch Neurol; 2007 May 05; 64(5):643-6. PubMed ID: 17502463
    [Abstract] [Full Text] [Related]

  • 5. Single-fiber EMG in familial hemiplegic migraine.
    Schoenen JE, Ambrosini A, de Noordhout AM.
    Neurology; 2005 May 10; 64(9):1666-7; author reply 1666-7. PubMed ID: 15883351
    [No Abstract] [Full Text] [Related]

  • 6. CACNA1A nonsense mutation is associated with basilar-type migraine and episodic ataxia type 2.
    Robbins MS, Lipton RB, Laureta EC, Grosberg BM.
    Headache; 2009 Jul 10; 49(7):1042-6. PubMed ID: 19486177
    [Abstract] [Full Text] [Related]

  • 7. [Is migraine a neuronal channelopothy?].
    Kwieciński H.
    Neurol Neurochir Pol; 2005 Jul 10; 39(4 Suppl 1):S61-4. PubMed ID: 16419572
    [Abstract] [Full Text] [Related]

  • 8. Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation.
    Chan YC, Burgunder JM, Wilder-Smith E, Chew SE, Lam-Mok-Sing KM, Sharma V, Ong BK.
    J Clin Neurosci; 2008 Aug 10; 15(8):891-4. PubMed ID: 18313928
    [Abstract] [Full Text] [Related]

  • 9. Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
    Freilinger T, Bohe M, Wegener B, Müller-Myhsok B, Dichgans M, Knoblauch H.
    Cephalalgia; 2008 Apr 10; 28(4):403-7. PubMed ID: 18279427
    [No Abstract] [Full Text] [Related]

  • 10. Commentary to 'Comorbidity in Finnish migraine families'.
    Russell MB.
    J Headache Pain; 2006 Oct 10; 7(5):320-1. PubMed ID: 17058042
    [No Abstract] [Full Text] [Related]

  • 11. New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus.
    Beauvais K, Cavé-Riant F, De Barace C, Tardieu M, Tournier-Lasserve E, Furby A.
    Eur Neurol; 2004 Oct 10; 52(1):58-61. PubMed ID: 15240985
    [No Abstract] [Full Text] [Related]

  • 12. [Familial hemiplegic migraine resulting in recurrent coma].
    Lee H, Aramideh M, Ginjaar HB.
    Ned Tijdschr Geneeskd; 2008 Feb 16; 152(7):393-6. PubMed ID: 18380388
    [Abstract] [Full Text] [Related]

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  • 14. Sporadic hemiplegic migraine in children.
    Pienczk-Reclawowicz K, Pilarska E, Lemka M.
    Neurol India; 2010 Feb 16; 58(4):512-3. PubMed ID: 20739784
    [No Abstract] [Full Text] [Related]

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  • 17. [Migraine: physiopathology, genetics and treatment aspects. The knowledge situation summarized].
    Ormstad H, Amthor KF.
    Lakartidningen; 2010 Feb 16; 105(30-31):2098-102. PubMed ID: 18751448
    [No Abstract] [Full Text] [Related]

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  • 20. Stepwise developmental regression associated with novel CACNA1A mutation.
    Guerin AA, Feigenbaum A, Donner EJ, Yoon G.
    Pediatr Neurol; 2008 Nov 16; 39(5):363-4. PubMed ID: 18940563
    [Abstract] [Full Text] [Related]

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