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 *

147 related articles for article (PubMed ID: 9612085)

  • 21. 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; 342(1-2):69-78. PubMed ID: 24836863
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Hypokalemic periodic paralysis and ataxia--Ca channel disorders].
    Konishi T
    No To Shinkei; 1997 Dec; 49(12):1068-78. PubMed ID: 9453037
    [No Abstract]   [Full Text] [Related]  

  • 23. New evidence for a genetic link between epilepsy and migraine.
    Winawer M
    Neurology; 2007 Jun; 68(23):1969-70. PubMed ID: 17548545
    [No Abstract]   [Full Text] [Related]  

  • 24. [Role of P/Q calcium channel in familial hemiplegic migraine].
    Weiss N; Tournier-Lasserve E; De Waard M
    Med Sci (Paris); 2007 Jan; 23(1):53-63. PubMed ID: 17212932
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Migraine and epilepsy: a focus on overlapping clinical, pathophysiological, molecular, and therapeutic aspects.
    Bianchin MM; Londero RG; Lima JE; Bigal ME
    Curr Pain Headache Rep; 2010 Aug; 14(4):276-83. PubMed ID: 20495966
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Familial hemiplegic migraine.
    Takeshima T; Adachi Y; Nakashima K
    Intern Med; 1998 Feb; 37(2):108-9. PubMed ID: 9550587
    [No Abstract]   [Full Text] [Related]  

  • 27. Familial hemiplegic migraine: involvement of a calcium neuronal channel.
    Ophoff RA; Terwindt GM; Vergouwe MN; Frants RR; Ferrari MD
    Neurologia; 1997 Dec; 12 Suppl 5():31-7. PubMed ID: 9436352
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Human epilepsy, episodic ataxia type 2, and migraine.
    Holtmann M; Opp J; Tokarzewski M; Korn-Merker E
    Lancet; 2002 Jan; 359(9301):170-1. PubMed ID: 11809294
    [No Abstract]   [Full Text] [Related]  

  • 29. Comorbidity of Migraine and Epilepsy in Pediatrics: A Review.
    Jancic J; Djuric V; Hencic B; van den Anker JN; Samardzic J
    J Child Neurol; 2018 Oct; 33(12):801-808. PubMed ID: 30095015
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [From gene to disease; from CACNA1A to migraine].
    Kors EE; Haan J; Frants RR; Ferrari MD
    Ned Tijdschr Geneeskd; 2001 Feb; 145(6):266-7. PubMed ID: 11236374
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The impact of pharmacogenetics for migraine.
    Ophoff RA; van den Maagdenberg AM; Roon KI; Ferrari MD; Frants RR
    Eur J Pharmacol; 2001 Feb; 413(1):1-10. PubMed ID: 11173058
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Cerebellar ataxia and absence epilepsy: genes, channels, neurons and mice].
    Sandoval-Romero A; Félix-Grijalva R
    Rev Neurol; 2003 Sep 1-15; 37(5):447-53. PubMed ID: 14533095
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The role of calcium channel mutations in human epilepsy.
    Gambardella A; Labate A
    Prog Brain Res; 2014; 213():87-96. PubMed ID: 25194484
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetics and pathology of voltage-gated Ca2+ channels.
    Ophoff RA; Terwindt GM; Ferrari MD; Frants RR
    Histol Histopathol; 1998 Jul; 13(3):827-36. PubMed ID: 9690139
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Calcium channels prove to be a real headache.
    Miller RJ
    Trends Neurosci; 1997 May; 20(5):189-92. PubMed ID: 9141192
    [No Abstract]   [Full Text] [Related]  

  • 36. Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
    Imbrici P; Jaffe SL; Eunson LH; Davies NP; Herd C; Robertson R; Kullmann DM; Hanna MG
    Brain; 2004 Dec; 127(Pt 12):2682-92. PubMed ID: 15483044
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Familial hemiplegic migraine type 1 mutations W1684R and V1696I alter G protein-mediated regulation of Ca(V)2.1 voltage-gated calcium channels.
    Garza-López E; Sandoval A; González-Ramírez R; Gandini MA; Van den Maagdenberg A; De Waard M; Felix R
    Biochim Biophys Acta; 2012 Aug; 1822(8):1238-46. PubMed ID: 22549042
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Eye movement disorders are an early manifestation of CACNA1A mutations in children.
    Tantsis EM; Gill D; Griffiths L; Gupta S; Lawson J; Maksemous N; Ouvrier R; Riant F; Smith R; Troedson C; Webster R; Menezes MP
    Dev Med Child Neurol; 2016 Jun; 58(6):639-44. PubMed ID: 26814174
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Absence epilepsy in tottering mutant mice is associated with calcium channel defects.
    Fletcher CF; Lutz CM; O'Sullivan TN; Shaughnessy JD; Hawkes R; Frankel WN; Copeland NG; Jenkins NA
    Cell; 1996 Nov; 87(4):607-17. PubMed ID: 8929530
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.
    Terwindt GM; Ophoff RA; Lindhout D; Haan J; Halley DJ; Sandkuijl LA; Brouwer OF; Frants RR; Ferrari MD
    Epilepsia; 1997 Aug; 38(8):915-21. PubMed ID: 9579893
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.