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 *

220 related articles for article (PubMed ID: 22883286)

  • 1. Variable manifestations of familial hemiplegic migraine associated with reversible cerebral edema in children.
    Asghar SJ; Milesi-Hallé A; Kaushik C; Glasier C; Sharp GB
    Pediatr Neurol; 2012 Sep; 47(3):201-4. PubMed ID: 22883286
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Opening of the blood-brain barrier preceding cortical edema in a severe attack of FHM type II.
    Dreier JP; Jurkat-Rott K; Petzold GC; Tomkins O; Klingebiel R; Kopp UA; Lehmann-Horn F; Friedman A; Dichgans M
    Neurology; 2005 Jun; 64(12):2145-7. PubMed ID: 15985592
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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; 15(8):891-4. PubMed ID: 18313928
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The genetic spectrum of a population-based sample of familial hemiplegic migraine.
    Thomsen LL; Kirchmann M; Bjornsson A; Stefansson H; Jensen RM; Fasquel AC; Petursson H; Stefansson M; Frigge ML; Kong A; Gulcher J; Stefansson K; Olesen J
    Brain; 2007 Feb; 130(Pt 2):346-56. PubMed ID: 17142831
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation.
    Iizuka T; Takahashi Y; Sato M; Yonekura J; Miyakawa S; Endo M; Hamada J; Kan S; Mochizuki H; Momose Y; Tsuji S; Sakai F
    J Neurol Neurosurg Psychiatry; 2012 Feb; 83(2):205-12. PubMed ID: 22013243
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene].
    Kors EE; Vanmolkot KR; Haan J; van den Maagdenberg AM; Frants RR; Ferrari MD
    Ned Tijdschr Geneeskd; 2004 Sep; 148(39):1919-20. PubMed ID: 15495990
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family.
    Spacey SD; Vanmolkot KR; Murphy C; van den Maagdenberg AM; Hsiung RG
    Headache; 2005 Oct; 45(9):1244-9. PubMed ID: 16178956
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Minor head trauma-induced sporadic hemiplegic migraine coma.
    Curtain RP; Smith RL; Ovcaric M; Griffiths LR
    Pediatr Neurol; 2006 Apr; 34(4):329-32. PubMed ID: 16638514
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2.
    Kors EE; Vanmolkot KR; Haan J; Kheradmand Kia S; Stroink H; Laan LA; Gill DS; Pascual J; van den Maagdenberg AM; Frants RR; Ferrari MD
    Neuropediatrics; 2004 Oct; 35(5):293-6. PubMed ID: 15534763
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [Familial hemiplegic migraine type 2: two paediatric case reports].
    Toledo-Bravo de Laguna L; Santana-Rodríguez A; Cabrera-López JC; Santana-Artiles A; Sebastián-García I
    Rev Neurol; 2012 Feb; 54(4):222-6. PubMed ID: 22314763
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biphasic neurovascular changes in prolonged migraine aura in familial hemiplegic migraine type 2.
    Iizuka T; Tominaga N; Kaneko J; Sato M; Akutsu T; Hamada J; Sakai F; Nishiyama K
    J Neurol Neurosurg Psychiatry; 2015 Mar; 86(3):344-53. PubMed ID: 25411546
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation.
    Pelzer N; Haan J; Stam AH; Vijfhuizen LS; Koelewijn SC; Smagge A; de Vries B; Ferrari MD; van den Maagdenberg AMJM; Terwindt GM
    Neurology; 2018 Feb; 90(7):e575-e582. PubMed ID: 29343472
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine.
    Tonelli A; Gallanti A; Bersano A; Cardin V; Ballabio E; Airoldi G; Redaelli F; Candelise L; Bresolin N; Bassi MT
    Clin Genet; 2007 Dec; 72(6):517-23. PubMed ID: 17877748
    [TBL] [Abstract][Full Text] [Related]  

  • 20. First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.
    Vanmolkot KR; Stam AH; Raman A; Koenderink JB; de Vries B; van den Boogerd EH; van Vark J; van den Heuvel JJ; Bajaj N; Terwindt GM; Haan J; Frants RR; Ferrari MD; van den Maagdenberg AM
    Eur J Hum Genet; 2007 Aug; 15(8):884-8. PubMed ID: 17473835
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.