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Results: 1-9 |
Results: 9

Authors: Hausler, MG Jaeken, J Monch, E Ramaekers, VT
Citation: Mg. Hausler et al., Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: Report on two siblings, NEUROPEDIAT, 32(4), 2001, pp. 191-195

Authors: Obermayer, N Busse, B Grunwald, A Monch, E Muller, C Neuhaus, P Gerlach, JC
Citation: N. Obermayer et al., Biochemical characterization of bioreactors for hybrid liver support: Serum-free liver cell coculture of nonparenchymal and parenchymal cells, TRANSPLAN P, 33(1-2), 2001, pp. 1930-1931

Authors: Hennermann, JB Vetter, B Wolf, C Windt, E Buhrdel, P Seidel, J Monch, E Kulozik, AE
Citation: Jb. Hennermann et al., Phenylketonuria and hyperphenylalaninemia in eastern Germany: A characteristic molecular profile and 15 novel mutations, HUM MUTAT, 15(3), 2000, pp. 254-260

Authors: Hundsdoerfer, P Vetter, B Stover, B Bassir, C Monch, E Ziemer, S Kulozik, AE
Citation: P. Hundsdoerfer et al., Design of a prospective neonatal cohort study of homozygous and double heterozygous Factor V Leiden and Factor II G20210A, KLIN PADIAT, 212(4), 2000, pp. 159-162

Authors: Vettermann, W Siedler, A Voss, L Monch, E Heckler, R Pauli, G
Citation: W. Vettermann et al., Spread of HIV infection in the general population in Germany, AIDS, 14(18), 2000, pp. 2949-2951

Authors: Monch, E
Citation: E. Monch, Phenylketonuria and hyperphenylalaninemia - Comment, MONATS KIND, 148(7), 2000, pp. 706-706

Authors: Burgard, P Bremer, HJ Buhrdel, P Clemens, PC Monch, E Przyrembel, H Trefz, FK Ullrich, K
Citation: P. Burgard et al., Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997, EUR J PED, 158(1), 1999, pp. 46-54

Authors: Maier, RF Witt, H Buhrer, C Monch, E Kottgen, E
Citation: Rf. Maier et al., HFE gene mutation and transferrin saturation in very low birthweight infants, ARCH DIS CH, 81(2), 1999, pp. F144-F145

Authors: Schwahn, B Wendel, U Schadewaldt, P Falkenberg, N Monch, E
Citation: B. Schwahn et al., Diurnal changes in plasma amino acids in maple syrup urine disease, ACT PAEDIAT, 87(12), 1998, pp. 1245-1246
Risultati: 1-9 |