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Journal Abstract Search

493 related items for PubMed ID: 19486177

  • 1. 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; 49(7):1042-6. PubMed ID: 19486177
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. A family of episodic ataxia type 2: no evidence of genetic linkage to the CACNA1A gene.
    Hirose H, Arayama T, Takita J, Igarashi T, Hayashi Y, Nagao Y.
    Int J Mol Med; 2003 Feb 05; 11(2):187-9. PubMed ID: 12525875
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  • 5. Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine.
    Kinder S, Ossig C, Wienecke M, Beyer A, von der Hagen M, Storch A, Smitka M.
    Eur J Paediatr Neurol; 2015 Jan 05; 19(1):72-4. PubMed ID: 25468264
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  • 6. Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits.
    Subramony SH, Schott K, Raike RS, Callahan J, Langford LR, Christova PS, Anderson JH, Gomez CM.
    Ann Neurol; 2003 Dec 05; 54(6):725-31. PubMed ID: 14681882
    [Abstract] [Full Text] [Related]

  • 7. Stepwise developmental regression associated with novel CACNA1A mutation.
    Guerin AA, Feigenbaum A, Donner EJ, Yoon G.
    Pediatr Neurol; 2008 Nov 05; 39(5):363-4. PubMed ID: 18940563
    [Abstract] [Full Text] [Related]

  • 8. Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation.
    Zangaladze A, Asadi-Pooya AA, Ashkenazi A, Sperling MR.
    Epilepsy Behav; 2010 Feb 05; 17(2):293-5. PubMed ID: 20071244
    [Abstract] [Full Text] [Related]

  • 9. Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A.
    García Segarra N, Gautschi I, Mittaz-Crettol L, Kallay Zetchi C, Al-Qusairi L, Van Bemmelen MX, Maeder P, Bonafé L, Schild L, Roulet-Perez E.
    J Neurol Sci; 2014 Jul 15; 342(1-2):69-78. PubMed ID: 24836863
    [Abstract] [Full Text] [Related]

  • 10. Progressive cerebellar ataxia with variable episodic symptoms--phenotypic diversity of R1668W CACNA1A mutation.
    Marti S, Baloh RW, Jen JC, Straumann D, Jung HH.
    Eur Neurol; 2008 Jul 15; 60(1):16-20. PubMed ID: 18437043
    [Abstract] [Full Text] [Related]

  • 11. Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large Portuguese family.
    Barros J, Damásio J, Tuna A, Alves I, Silveira I, Pereira-Monteiro J, Sequeiros J, Alonso I, Sousa A, Coutinho P.
    JAMA Neurol; 2013 Feb 15; 70(2):235-40. PubMed ID: 23407676
    [Abstract] [Full Text] [Related]

  • 12. CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.
    Stam AH, Vanmolkot KR, Kremer HP, Gärtner J, Brown J, Leshinsky-Silver E, Gilad R, Kors EE, Frankhuizen WS, Ginjaar HB, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM, Terwindt GM.
    Clin Genet; 2008 Nov 15; 74(5):481-5. PubMed ID: 18400034
    [Abstract] [Full Text] [Related]

  • 13. [From gene to disease; from CACNA1A to migraine].
    Kors EE, Haan J, Frants RR, Ferrari MD.
    Ned Tijdschr Geneeskd; 2001 Feb 10; 145(6):266-7. PubMed ID: 11236374
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  • 16. Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.
    Cricchi F, Di Lorenzo C, Grieco GS, Rengo C, Cardinale A, Racaniello M, Santorelli FM, Nappi G, Pierelli F, Casali C.
    J Neurol Sci; 2007 Mar 15; 254(1-2):69-71. PubMed ID: 17292920
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  • 17. [Molecular genetic findings in migraine].
    Østergaard E, Thomsen LL, Russell MB.
    Ugeskr Laeger; 2001 Nov 05; 163(45):6260-5. PubMed ID: 11723684
    [Abstract] [Full Text] [Related]

  • 18. 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 05; 23(1):7-10. PubMed ID: 12111614
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  • 20. 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
    [Abstract] [Full Text] [Related]

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