These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 19438926)

  • 21. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 54(3):360-6. PubMed ID: 12953268
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Detection of a novel mutation in the CACNA1A gene.
    Stuart S; Roy B; Davies G; Maksemous N; Smith R; Griffiths LR
    Twin Res Hum Genet; 2012 Feb; 15(1):120-5. PubMed ID: 22784462
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation.
    Malpas TJ; Riant F; Tournier-Lasserve E; Vahedi K; Neville BG
    Dev Med Child Neurol; 2010 Jan; 52(1):103-4. PubMed ID: 19811514
    [No Abstract]   [Full Text] [Related]  

  • 25. 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; 70(2):235-40. PubMed ID: 23407676
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Head tremor related to CACNA1A mutations.
    Geerlings RP; Koehler PJ; Haane DY; Stam AH; de Vries B; Boon EM; Haan J
    Cephalalgia; 2011 Sep; 31(12):1315-9. PubMed ID: 21768184
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Genetics of migraine].
    Ducros A
    Pathol Biol (Paris); 2000 Sep; 48(7):658-62. PubMed ID: 11072644
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1.
    Eikermann-Haerter K; Dileköz E; Kudo C; Savitz SI; Waeber C; Baum MJ; Ferrari MD; van den Maagdenberg AM; Moskowitz MA; Ayata C
    J Clin Invest; 2009 Jan; 119(1):99-109. PubMed ID: 19104150
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraine.
    Sánchez-Albisua I; Schöning M; Jurkat-Rott K; Lerche H
    Pediatr Neurol; 2013 Oct; 49(4):286-8. PubMed ID: 23831250
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Molecular genetic findings in migraine].
    Østergaard E; Thomsen LL; Russell MB
    Ugeskr Laeger; 2001 Nov; 163(45):6260-5. PubMed ID: 11723684
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
    Ambrosini A; D'Onofrio M; Grieco GS; Di Mambro A; Montagna G; Fortini D; Nicoletti F; Nappi G; Sances G; Schoenen J; Buzzi MG; Santorelli FM; Pierelli F
    Neurology; 2005 Dec; 65(11):1826-8. PubMed ID: 16344534
    [TBL] [Abstract][Full Text] [Related]  

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

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

  • 34. 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; 23(1):7-10. PubMed ID: 12111614
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline.
    Freilinger T; Ackl N; Ebert A; Schmidt C; Rautenstrauss B; Dichgans M; Danek A
    J Neurol Sci; 2011 Jan; 300(1-2):160-3. PubMed ID: 21035146
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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; 241(1-2):13-7. PubMed ID: 16325861
    [TBL] [Abstract][Full Text] [Related]  

  • 37. RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice.
    de Vries B; Eising E; Broos LA; Koelewijn SC; Todorov B; Frants RR; Boer JM; Ferrari MD; Hoen PA; van den Maagdenberg AM
    Cephalalgia; 2014 Mar; 34(3):174-82. PubMed ID: 23985897
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.
    Lebas A; Guyant-Maréchal L; Hannequin D; Riant F; Tournier-Lasserve E; Parain D
    Cephalalgia; 2008 Jul; 28(7):774-7. PubMed ID: 18498390
    [TBL] [Abstract][Full Text] [Related]  

  • 39. CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.
    Romozzi M; Primiano G; Rollo E; Travaglini L; Calabresi P; Servidei S; Vollono C
    J Headache Pain; 2021 Jul; 22(1):85. PubMed ID: 34320921
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility.
    D'Onofrio M; Ambrosini A; Di Mambro A; Arisi I; Santorelli FM; Grieco GS; Nicoletti F; Nappi G; Pierelli F; Schoenen J; Buzzi MG
    Neurosci Lett; 2009 Mar; 453(1):12-5. PubMed ID: 19429006
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.