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Results: 1-5 |
Results: 5

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: Muller, P Reichenbach, H Mockel, A Buhrdel, P
Citation: P. Muller et al., I-cell disease complicated by unusual dilatative cardiomyopathy, J INH MET D, 23(5), 2000, pp. 514-516

Authors: Hoepffner, W Wiemert, B Reitmann, M Raue, W Buhrdel, P Kiess, W
Citation: W. Hoepffner et al., Paediatric emergency outpatient care. Analysis of an university hospital-based service, MONATS KIND, 148(5), 2000, pp. 470-474

Authors: Muller, P Reichenbach, H Berthold, A Buhrdel, P
Citation: P. Muller et al., Images of the month - Mucolipidosis II (I-cell disease), MONATS KIND, 148(5), 2000, pp. 494-495

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
Risultati: 1-5 |