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Journal Abstract Search

220 related items for PubMed ID: 12548383

  • 1. Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro.
    Klepper J, Flörcken A, Fischbarg J, Voit T.
    Eur J Pediatr; 2003 Feb; 162(2):84-9. PubMed ID: 12548383
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  • 4. Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndrome.
    Coman DJ, Sinclair KG, Burke CJ, Appleton DB, Pelekanos JT, O'Neil CM, Wallace GB, Bowling FG, Wang D, De Vivo DC, McGill JJ.
    J Paediatr Child Health; 2006 May; 42(5):263-7. PubMed ID: 16712556
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  • 5. Glucose transporter type 1 deficiency syndrome (Glut1DS): methylxanthines potentiate GLUT1 haploinsufficiency in vitro.
    Ho YY, Yang H, Klepper J, Fischbarg J, Wang D, De Vivo DC.
    Pediatr Res; 2001 Aug; 50(2):254-60. PubMed ID: 11477212
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  • 6. 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
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  • 7. Human erythrocyte sugar transport is incompatible with available carrier models.
    Cloherty EK, Heard KS, Carruthers A.
    Biochemistry; 1996 Aug 13; 35(32):10411-21. PubMed ID: 8756697
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  • 9. [The ketogenic diet in German-speaking countries: update 2003].
    Klepper J, Leiendecker B, Riemann E, Baumeister FA.
    Klin Padiatr; 2004 Aug 13; 216(5):277-85. PubMed ID: 15455294
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  • 11. Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain-- a review.
    Klepper J, Voit T.
    Eur J Pediatr; 2002 Jun 13; 161(6):295-304. PubMed ID: 12029447
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  • 15. Glucose transporter 1 deficiency syndrome and other glycolytic defects.
    De Vivo DC, Leary L, Wang D.
    J Child Neurol; 2002 Dec 13; 17 Suppl 3():3S15-23; discussion 3S24-5. PubMed ID: 12597052
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  • 16. 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 13; 27(4):311-7. PubMed ID: 15862198
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  • 17. Properties of the human erythrocyte glucose transport protein are determined by cellular context.
    Levine KB, Robichaud TK, Hamill S, Sultzman LA, Carruthers A.
    Biochemistry; 2005 Apr 19; 44(15):5606-16. PubMed ID: 15823019
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  • 18. Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.
    Wang D, Pascual JM, Yang H, Engelstad K, Jhung S, Sun RP, De Vivo DC.
    Ann Neurol; 2005 Jan 19; 57(1):111-8. PubMed ID: 15622525
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  • 19. Bench meets bedside: a 10-year-old girl and amino acid residue glycine 75 of the facilitative glucose transporter GLUT1.
    Klepper J, Salas-Burgos A, Gertsen E, Fischbarg J.
    Biochemistry; 2005 Sep 27; 44(38):12621-6. PubMed ID: 16171377
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  • 20. GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier.
    Seidner G, Alvarez MG, Yeh JI, O'Driscoll KR, Klepper J, Stump TS, Wang D, Spinner NB, Birnbaum MJ, De Vivo DC.
    Nat Genet; 1998 Feb 27; 18(2):188-91. PubMed ID: 9462754
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