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Results: 1-8 |
Results: 8

Authors: Klepper, J Willemsen, M Verrips, A Guertsen, E Herrmann, R Kutzick, C Florcken, A Voit, T
Citation: J. Klepper et al., Autosomal dominant transmission of GLUT1 deficiency, HUM MOL GEN, 10(1), 2001, pp. 63-68

Authors: Ho, YY Yang, H Klepper, J Fischbarg, J Wang, D De Vivo, DC
Citation: Yy. Ho et al., Glucose transporter type 1 deficiency syndrome (Glut1DS): Methylxanthines potentiate GLUT1 haploinsufficiency in vitro, PEDIAT RES, 50(2), 2001, pp. 254-260

Authors: Klepper, J Monden, I Guertsen, E Voit, T Willemsen, M Keller, K
Citation: J. Klepper et al., Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene, FEBS LETTER, 498(1), 2001, pp. 104-109

Authors: Klepper, J Santer, R Baethmann, M De Vivo, DC Voit, T
Citation: J. Klepper et al., Congenital defects of glucose transport, MONATS KIND, 148(1), 2000, pp. 2-11

Authors: Klepper, J Garcia-Alvarez, M O'Driscoll, KR Parides, MK Wang, D Ho, YY De Vivo, DC
Citation: J. Klepper et al., Erythrocyte 3-O-methyl-D-glucose uptake assay for diagnosis of glucose-transporter-protein syndrome, J CL LAB AN, 13(3), 1999, pp. 116-121

Authors: Klepper, J Wang, D Fischbarg, J Vera, JC Jarjour, IT O'Driscoll, KR De Vivo, DC
Citation: J. Klepper et al., Defective glucose transport across brain tissue barriers: A newly recognized neurological syndrome, NEUROCHEM R, 24(4), 1999, pp. 587-594

Authors: Klepper, J Fischbarg, J Vera, JC Wang, D De Vivo, DC
Citation: J. Klepper et al., GLUT1-deficiency: Barbiturates potentiate haploinsufficiency in vitro, PEDIAT RES, 46(6), 1999, pp. 677-683

Authors: Klepper, J Busse, M Strassburg, HM Sorensen, N
Citation: J. Klepper et al., Epilepsy in shunt-treated hydrocephalus, DEVELOP MED, 40(11), 1998, pp. 731-736
Risultati: 1-8 |