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 *

271 related articles for article (PubMed ID: 19798636)

  • 1. Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1.
    Suls A; Mullen SA; Weber YG; Verhaert K; Ceulemans B; Guerrini R; Wuttke TV; Salvo-Vargas A; Deprez L; Claes LR; Jordanova A; Berkovic SF; Lerche H; De Jonghe P; Scheffer IE
    Ann Neurol; 2009 Sep; 66(3):415-9. PubMed ID: 19798636
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency.
    Mullen SA; Suls A; De Jonghe P; Berkovic SF; Scheffer IE
    Neurology; 2010 Aug; 75(5):432-40. PubMed ID: 20574033
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
    Leen WG; Klepper J; Verbeek MM; Leferink M; Hofste T; van Engelen BG; Wevers RA; Arthur T; Bahi-Buisson N; Ballhausen D; Bekhof J; van Bogaert P; Carrilho I; Chabrol B; Champion MP; Coldwell J; Clayton P; Donner E; Evangeliou A; Ebinger F; Farrell K; Forsyth RJ; de Goede CG; Gross S; Grunewald S; Holthausen H; Jayawant S; Lachlan K; Laugel V; Leppig K; Lim MJ; Mancini G; Marina AD; Martorell L; McMenamin J; Meuwissen ME; Mundy H; Nilsson NO; Panzer A; Poll-The BT; Rauscher C; Rouselle CM; Sandvig I; Scheffner T; Sheridan E; Simpson N; Sykora P; Tomlinson R; Trounce J; Webb D; Weschke B; Scheffer H; Willemsen MA
    Brain; 2010 Mar; 133(Pt 3):655-70. PubMed ID: 20129935
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Paroxysmal exercise-induced dyskinesia, writer's cramp, migraine with aura and absence epilepsy in twin brothers with a novel SLC2A1 missense mutation.
    Urbizu A; Cuenca-León E; Raspall-Chaure M; Gratacòs M; Conill J; Redecillas S; Roig-Quilis M; Macaya A
    J Neurol Sci; 2010 Aug; 295(1-2):110-3. PubMed ID: 20621801
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.
    Mullen SA; Marini C; Suls A; Mei D; Della Giustina E; Buti D; Arsov T; Damiano J; Lawrence K; De Jonghe P; Berkovic SF; Scheffer IE; Guerrini R
    Arch Neurol; 2011 Sep; 68(9):1152-5. PubMed ID: 21555602
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.
    Arsov T; Mullen SA; Damiano JA; Lawrence KM; Huh LL; Nolan M; Young H; Thouin A; Dahl HH; Berkovic SF; Crompton DE; Sadleir LG; Scheffer IE
    Epilepsia; 2012 Dec; 53(12):e204-7. PubMed ID: 23106342
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?
    Becker F; Schubert J; Weckhuysen S; Suls A; Grüninger S; Korn-Merker E; Hofmann-Peters A; Sperner J; Cross H; Hallmann K; Elger CE; Kunz WS; Madeleyen R; Lerche H; Weber YG
    Epilepsy Res; 2015 Aug; 114():47-51. PubMed ID: 26088884
    [TBL] [Abstract][Full Text] [Related]  

  • 8. "Benign" myoclonic epilepsy of infancy as the initial presentation of glucose transporter-1 deficiency.
    Gaspard N; Suls A; Vilain C; De Jonghe P; Van Bogaert P
    Epileptic Disord; 2011 Sep; 13(3):300-3. PubMed ID: 21865127
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mild adolescent/adult onset epilepsy and paroxysmal exercise-induced dyskinesia due to GLUT1 deficiency.
    Afawi Z; Suls A; Ekstein D; Kivity S; Neufeld MY; Oliver K; De Jonghe P; Korczyn AD; Berkovic SF
    Epilepsia; 2010 Dec; 51(12):2466-9. PubMed ID: 21204808
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic diet.
    Klepper J
    Epilepsia; 2008 Nov; 49 Suppl 8():46-9. PubMed ID: 19049586
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.
    Arsov T; Mullen SA; Rogers S; Phillips AM; Lawrence KM; Damiano JA; Goldberg-Stern H; Afawi Z; Kivity S; Trager C; Petrou S; Berkovic SF; Scheffer IE
    Ann Neurol; 2012 Nov; 72(5):807-15. PubMed ID: 23280796
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Seizure control and acceptance of the ketogenic diet in GLUT1 deficiency syndrome: a 2- to 5-year follow-up of 15 children enrolled prospectively.
    Klepper J; Scheffer H; Leiendecker B; Gertsen E; Binder S; Leferink M; Hertzberg C; Näke A; Voit T; Willemsen MA
    Neuropediatrics; 2005 Oct; 36(5):302-8. PubMed ID: 16217704
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The role of SLC2A1 in early onset and childhood absence epilepsies.
    Muhle H; Helbig I; Frøslev TG; Suls A; von Spiczak S; Klitten LL; Dahl HA; Brusgaard K; Neubauer B; De Jonghe P; Tommerup N; Stephani U; Hjalgrim H; Møller RS
    Epilepsy Res; 2013 Jul; 105(1-2):229-33. PubMed ID: 23306390
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome.
    Larsen J; Johannesen KM; Ek J; Tang S; Marini C; Blichfeldt S; Kibaek M; von Spiczak S; Weckhuysen S; Frangu M; Neubauer BA; Uldall P; Striano P; Zara F; ; Kleiss R; Simpson M; Muhle H; Nikanorova M; Jepsen B; Tommerup N; Stephani U; Guerrini R; Duno M; Hjalgrim H; Pal D; Helbig I; Møller RS
    Epilepsia; 2015 Dec; 56(12):e203-8. PubMed ID: 26537434
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The expanding phenotype of GLUT1-deficiency syndrome.
    Brockmann K
    Brain Dev; 2009 Aug; 31(7):545-52. PubMed ID: 19304421
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Glucose transporter-1 (GLUT1) deficiency syndrome: diagnosis and treatment in late childhood.
    Gramer G; Wolf NI; Vater D; Bast T; Santer R; Kamsteeg EJ; Wevers RA; Ebinger F
    Neuropediatrics; 2012 Jun; 43(3):168-71. PubMed ID: 22622956
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Absence of mutation in the SLC2A1 gene in a cohort of patients with alternating hemiplegia of childhood (AHC).
    Vuillaumier-Barrot S; Panagiotakaki E; Le Bizec C; El Baba C; ; Fontaine B; Arzimanoglou A; Seta N; Nicole S
    Neuropediatrics; 2010 Dec; 41(6):267-9. PubMed ID: 21445818
    [TBL] [Abstract][Full Text] [Related]  

  • 18. GLUT1 deficiency syndrome--2007 update.
    Klepper J; Leiendecker B
    Dev Med Child Neurol; 2007 Sep; 49(9):707-16. PubMed ID: 17718830
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Glut1 deficiency syndrome: Absence epilepsy and La Soupe du Jour.
    Thouin A; Crompton DE
    Pract Neurol; 2016 Feb; 16(1):50-2. PubMed ID: 26336901
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Glucose transporter type 1 deficiency syndrome with carbohydrate-responsive symptoms but without epilepsy.
    Koy A; Assmann B; Klepper J; Mayatepek E
    Dev Med Child Neurol; 2011 Dec; 53(12):1154-6. PubMed ID: 21838819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.