BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 24097848)

  • 1. A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
    Al-Bulushi B; Al-Hashem A; Tabarki B
    J Child Neurol; 2014 Feb; 29(2):265-8. PubMed ID: 24097848
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.
    Swoboda KJ; Kanavakis E; Xaidara A; Johnson JE; Leppert MF; Schlesinger-Massart MB; Ptacek LJ; Silver K; Youroukos S
    Ann Neurol; 2004 Jun; 55(6):884-7. PubMed ID: 15174025
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.
    Costa C; Prontera P; Sarchielli P; Tonelli A; Bassi MT; Cupini LM; Caproni S; Siliquini S; Donti E; Calabresi P
    Cephalalgia; 2014 Jan; 34(1):68-72. PubMed ID: 23918834
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.
    de Vries B; Stam AH; Kirkpatrick M; Vanmolkot KR; Koenderink JB; van den Heuvel JJ; Stunnenberg B; Goudie D; Shetty J; Jain V; van Vark J; Terwindt GM; Frants RR; Haan J; van den Maagdenberg AM; Ferrari MD
    Epilepsia; 2009 Nov; 50(11):2503-4. PubMed ID: 19874388
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 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. An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2.
    Wilbur C; Buerki SE; Guella I; Toyota EB; Evans DM; McKenzie MB; Datta A; Michoulas A; Adam S; Van Allen MI; Nelson TN; Farrer MJ; Connolly MB; Demos M
    Pediatr Neurol; 2017 Oct; 75():87-90. PubMed ID: 28811059
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
    Vetro A; Nielsen HN; Holm R; Hevner RF; Parrini E; Powis Z; Møller RS; Bellan C; Simonati A; Lesca G; Helbig KL; Palmer EE; Mei D; Ballardini E; Van Haeringen A; Syrbe S; Leuzzi V; Cioni G; Curry CJ; Costain G; Santucci M; Chong K; Mancini GMS; Clayton-Smith J; Bigoni S; Scheffer IE; Dobyns WB; Vilsen B; Guerrini R;
    Brain; 2021 Jun; 144(5):1435-1450. PubMed ID: 33880529
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsy.
    Pisano T; Spiller S; Mei D; Guerrini R; Cianchetti C; Friedrich T; Pruna D
    Cephalalgia; 2013 Dec; 33(16):1302-10. PubMed ID: 23838748
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
    Calame DG; Houck K; Lotze T; Emrick L; Parnes M
    Eur J Paediatr Neurol; 2021 Mar; 31():21-26. PubMed ID: 33578253
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation.
    De Cunto A; Bensa M; Tonelli A
    Pediatr Neurol; 2012 Aug; 47(2):133-6. PubMed ID: 22759692
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patients.
    Dai L; Ding C; Tian X; Liu M; Ma Y; Chen C; Ren X; Li H
    Brain Dev; 2023 Sep; 45(8):422-431. PubMed ID: 37142513
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.
    Roth C; Freilinger T; Kirovski G; Dunkel J; Shah Y; Wilken B; Rautenstrauß B; Ferbert A
    Cephalalgia; 2014 Mar; 34(3):183-90. PubMed ID: 24096472
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood.
    Bassi MT; Bresolin N; Tonelli A; Nazos K; Crippa F; Baschirotto C; Zucca C; Bersano A; Dolcetta D; Boneschi FM; Barone V; Casari G
    J Med Genet; 2004 Aug; 41(8):621-8. PubMed ID: 15286158
    [No Abstract]   [Full Text] [Related]  

  • 17. Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.
    Castro MJ; Nunes B; de Vries B; Lemos C; Vanmolkot KR; van den Heuvel JJ; Temudo T; Barros J; Sequeiros J; Frants RR; Koenderink JB; Pereira-Monteiro JM; van den Maagdenberg AM
    Clin Genet; 2008 Jan; 73(1):37-43. PubMed ID: 18028456
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Epilepsy as part of the phenotype associated with ATP1A2 mutations.
    Deprez L; Weckhuysen S; Peeters K; Deconinck T; Claeys KG; Claes LR; Suls A; Van Dyck T; Palmini A; Matthijs G; Van Paesschen W; De Jonghe P
    Epilepsia; 2008 Mar; 49(3):500-8. PubMed ID: 18028407
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation.
    De Sanctis S; Grieco GS; Breda L; Casali C; Nozzi M; Del Torto M; Chiarelli F; Verrotti A
    Headache; 2011 Mar; 51(3):447-450. PubMed ID: 21352219
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.