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Results: 1-9 |
Results: 9
Patent ductus venosus does not lead to alimentary galactosaemia in preterminfants
Authors: Fugelseth, D Guthenberg, C Hagenfeldt, L Liestol, K Hallerud, M Lindemann, R
Citation: D. Fugelseth et al., Patent ductus venosus does not lead to alimentary galactosaemia in preterminfants, ACT PAEDIAT, 90(2), 2001, pp. 192-195
Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infants
Authors: Nordenstrom, A Wedell, A Hagenfeldt, L Marcus, C Larsson, A
Citation: A. Nordenstrom et al., Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infants, PEDIATRICS, 108(4), 2001, pp. NIL_66-NIL_73
Aberrant tyrosine transport across the cell membrane in patients with schizophrenia
Authors: Flyckt, L Venizelos, N Edman, G Bjerkenstedt, L Hagenfeldt, L Wiesel, FA
Citation: L. Flyckt et al., Aberrant tyrosine transport across the cell membrane in patients with schizophrenia, ARCH G PSYC, 58(10), 2001, pp. 953-958
D-2-hydroxyglutaric aciduria with cerebral, vascular, and muscular abnormalities in a 14-year-old boy
Authors: Eeg-Olofsson, O Zhang, WW Olsson, Y Jagell, S Hagenfeldt, L
Citation: O. Eeg-olofsson et al., D-2-hydroxyglutaric aciduria with cerebral, vascular, and muscular abnormalities in a 14-year-old boy, J CHILD NEU, 15(7), 2000, pp. 488-492
Tyrosine transport is regulated differently in patients with schizophrenia
Authors: Wiesel, FA Andersson, JLR Westerberg, G Wieselgren, IM Bjerkenstedt, L Hagenfeldt, L Langstrom, B
Citation: Fa. Wiesel et al., Tyrosine transport is regulated differently in patients with schizophrenia, SCHIZOPHR R, 40(1), 1999, pp. 37-42
Prevalence of the 985A > G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in Sweden
Authors: Johansson, A Guthenberg, C Ahlman, H Von Dobeln, U Hagenfeldt, L
Citation: A. Johansson et al., Prevalence of the 985A > G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in Sweden, SC J CL INV, 59(4), 1999, pp. 289-291
Synthesis of mevalonate pathway lipids in fibroblasts from Zellweger and X-linked ALD patients
Authors: Appelkvist, EL Venizelos, N Zhang, YY Parmryd, I Hagenfeldt, L Dallner, G
Citation: El. Appelkvist et al., Synthesis of mevalonate pathway lipids in fibroblasts from Zellweger and X-linked ALD patients, PEDIAT RES, 46(3), 1999, pp. 345-350
Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency
Authors: Nordenstrom, A Thilen, A Hagenfeldt, L Larsson, A Wedell, A
Citation: A. Nordenstrom et al., Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency, J CLIN END, 84(5), 1999, pp. 1505-1509
Improved peripheral nerve conduction, EEG and verbal IQ after bone marrow transplantation for adult metachromatic leukodystrophy
Authors: Solders, G Celsing, G Hagenfeldt, L Ljungman, P Isberg, B Ringden, O
Citation: G. Solders et al., Improved peripheral nerve conduction, EEG and verbal IQ after bone marrow transplantation for adult metachromatic leukodystrophy, BONE MAR TR, 22(11), 1998, pp. 1119-1122
Risultati: 1-9 |