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 *

124 related articles for article (PubMed ID: 12849225)

  • 61. Physical mapping and characterization of the human Na,K-ATPase isoform, ATP1A4.
    Keryanov S; Gardner KL
    Gene; 2002 Jun; 292(1-2):151-66. PubMed ID: 12119109
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.
    Todt U; Dichgans M; Jurkat-Rott K; Heinze A; Zifarelli G; Koenderink JB; Goebel I; Zumbroich V; Stiller A; Ramirez A; Friedrich T; Göbel H; Kubisch C
    Hum Mutat; 2005 Oct; 26(4):315-21. PubMed ID: 16110494
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13.
    Noble-Topham SE; Dyment DA; Cader MZ; Ganapathy R; Brown JD; Rice GP; Ebers GC
    Neurology; 2002 Oct; 59(7):1099-101. PubMed ID: 12370474
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testing.
    Wieser T; Mueller C; Evers S; Zierz S; Deufel T
    Clin Chem Lab Med; 2003 Mar; 41(3):272-5. PubMed ID: 12705332
    [TBL] [Abstract][Full Text] [Related]  

  • 65. 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; 345(1):17-24. PubMed ID: 11439943
    [TBL] [Abstract][Full Text] [Related]  

  • 66. A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.
    Gallanti A; Tonelli A; Cardin V; Bussone G; Bresolin N; Bassi MT
    J Neurol Sci; 2008 Oct; 273(1-2):123-6. PubMed ID: 18644608
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
    Kors EE; Terwindt GM; Vermeulen FL; Fitzsimons RB; Jardine PE; Heywood P; Love S; van den Maagdenberg AM; Haan J; Frants RR; Ferrari MD
    Ann Neurol; 2001 Jun; 49(6):753-60. PubMed ID: 11409427
    [TBL] [Abstract][Full Text] [Related]  

  • 68. The genetics of migraine.
    Ducros A; Tournier-Lasserve E; Bousser MG
    Lancet Neurol; 2002 Sep; 1(5):285-93. PubMed ID: 12849426
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Acute encephalopathy in familial hemiplegic migraine with ATP1A2 mutation.
    Merwick A; Fernandez D; McNamara B; Harrington H
    BMJ Case Rep; 2013 Jun; 2013():. PubMed ID: 23761507
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Transient nonverbal learning disorder in a child suffering from Familial Hemiplegic Migraine.
    Podestà B; Briatore E; Boghi A; Marenco D; Calzolari S
    Cephalalgia; 2011 Oct; 31(14):1497-502. PubMed ID: 21908445
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine.
    Tavraz NN; Dürr KL; Koenderink JB; Freilinger T; Bamberg E; Dichgans M; Friedrich T
    Channels (Austin); 2009; 3(2):82-7. PubMed ID: 19372756
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine.
    Kaube H; Herzog J; Käufer T; Dichgans M; Diener HC
    Neurology; 2000 Jul; 55(1):139-41. PubMed ID: 10891926
    [TBL] [Abstract][Full Text] [Related]  

  • 73. [Familial hemiplegic migraine of childhood].
    Livne A; Lahat E
    Harefuah; 1999 Aug; 137(3-4):101-4, 175. PubMed ID: 10959293
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Genetics of migraine: an update with special attention to genetic comorbidity.
    Stam AH; van den Maagdenberg AM; Haan J; Terwindt GM; Ferrari MD
    Curr Opin Neurol; 2008 Jun; 21(3):288-93. PubMed ID: 18451712
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Biochemical characterization of sporadic/familial hemiplegic migraine mutations.
    Weigand KM; Swarts HG; Russel FG; Koenderink JB
    Biochim Biophys Acta; 2014 Jul; 1838(7):1693-700. PubMed ID: 24704353
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Intravenous Nimodipine Treatment for Severe Episode of ATP1A2 Hemiplegic Migraine.
    Dannenberg F; Prager C; Schmidt F; Tietze A; Bittigau P; Kaindl AM
    Pediatr Neurol; 2020 Nov; 112():71-72. PubMed ID: 32920306
    [No Abstract]   [Full Text] [Related]  

  • 77. Perfusion and pH MRI in familial hemiplegic migraine with prolonged aura.
    Blicher JU; Tietze A; Donahue MJ; Smith SA; Østergaard L
    Cephalalgia; 2016 Mar; 36(3):279-83. PubMed ID: 25948653
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Basilar-type migraine: clinical, epidemiologic, and genetic features.
    Kirchmann M; Thomsen LL; Olesen J
    Neurology; 2006 Mar; 66(6):880-6. PubMed ID: 16567706
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Another migraine gene.
    Goadsby PJ; Kullmann DM
    Lancet; 2005 Jul 30-Aug 5; 366(9483):345-6. PubMed ID: 16054921
    [No Abstract]   [Full Text] [Related]  

  • 80. [Molecular mechanism of migraine].
    Moskowitz MA
    Rinsho Shinkeigaku; 2008 Nov; 48(11):798. PubMed ID: 19198086
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.