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Journal Abstract Search

300 related items for PubMed ID: 16149086

  • 21. Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic diet.
    Klepper J.
    Epilepsia; 2008 Nov; 49 Suppl 8():46-9. PubMed ID: 19049586
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  • 25. 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
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  • 27. GLUT1 deficiency syndrome 2013: current state of the art.
    De Giorgis V, Veggiotti P.
    Seizure; 2013 Dec; 22(10):803-11. PubMed ID: 23890838
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  • 29. 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
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  • 32. The glucose transporter type 1 (Glut1) syndromes.
    Koch H, Weber YG.
    Epilepsy Behav; 2019 Feb; 91():90-93. PubMed ID: 30076047
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  • 33. 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
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  • 34. The many faces of Glut1 deficiency syndrome.
    Tzadok M, Nissenkorn A, Porper K, Matot I, Marcu S, Anikster Y, Menascu S, Bercovich D, Ben Zeev B.
    J Child Neurol; 2014 Mar; 29(3):349-59. PubMed ID: 23340081
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  • 35. Phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS).
    Pearson TS, Akman C, Hinton VJ, Engelstad K, De Vivo DC.
    Curr Neurol Neurosci Rep; 2013 Apr; 13(4):342. PubMed ID: 23443458
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  • 36. GLUT1 Deficiency Syndrome-Early Treatment Maintains Cognitive Development? (Literature Review and Case Report).
    Kolic I, Radic Nisevic J, Vlasic Cicvaric I, Butorac Ahel I, Lah Tomulic K, Segulja S, Baraba Dekanic K, Serifi S, Ovuka A, Prpic I.
    Genes (Basel); 2021 Aug 31; 12(9):. PubMed ID: 34573360
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  • 39. Clinical presentation, EEG studies, and novel mutations in two cases of GLUT1 deficiency syndrome in Japan.
    Ito Y, Gertsen E, Oguni H, Nakayama T, Matsuo M, Funatsuka M, Voit T, Klepper J, Osawa M.
    Brain Dev; 2005 Jun 31; 27(4):311-7. PubMed ID: 15862198
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  • 40. Sepiapterin reductase deficiency: a treatable mimic of cerebral palsy.
    Friedman J, Roze E, Abdenur JE, Chang R, Gasperini S, Saletti V, Wali GM, Eiroa H, Neville B, Felice A, Parascandalo R, Zafeiriou DI, Arrabal-Fernandez L, Dill P, Eichler FS, Echenne B, Gutierrez-Solana LG, Hoffmann GF, Hyland K, Kusmierska K, Tijssen MA, Lutz T, Mazzuca M, Penzien J, Poll-The BT, Sykut-Cegielska J, Szymanska K, Thöny B, Blau N.
    Ann Neurol; 2012 Apr 31; 71(4):520-30. PubMed ID: 22522443
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