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Results: 1-18 |
Results: 18
Individual blood-brain barrier phenylalanine transport determines clinicaloutcome in phenylketonuria
Authors: Weglage, J Wiedermann, D Denecke, J Feldmann, R Koch, HG Ullrich, K Harms, E Moller, HE
Citation: J. Weglage et al., Individual blood-brain barrier phenylalanine transport determines clinicaloutcome in phenylketonuria, ANN NEUROL, 50(4), 2001, pp. 463-467
The CLAS Cherenkov detector
Authors: Adams, G Burkert, V Carl, R Carstens, T Frolov, V Houghtlin, L Jacobs, G Kossov, M Klusman, M Kross, B Onuk, M Napolitano, J Price, JW Riggs, C Sharabian, Y Stavinsky, A Smith, LC Stephens, WA Stoler, P Tuzel, W Ullrich, K Vlassov, A Weisenberger, A Witkowski, M Wojtekhowski, B Yergin, PF Zorn, C
Citation: G. Adams et al., The CLAS Cherenkov detector, NUCL INST A, 465(2-3), 2001, pp. 414-427
Kinetics and diffusion of defects in fayalite, Fe2SiO4
Authors: Ullrich, K Becker, KD
Citation: K. Ullrich et Kd. Becker, Kinetics and diffusion of defects in fayalite, Fe2SiO4, SOL ST ION, 141, 2001, pp. 307-312
Normal clinical outcome in untreated subjects with mild hyperphenylalaninemia
Authors: Weglage, J Pietsch, M Feldmann, R Koch, HG Zschocke, J Hoffmann, G Muntau-Heger, A Denecke, J Guldberg, P Guttler, F Moller, H Wendel, U Ullrich, K Harms, E
Citation: J. Weglage et al., Normal clinical outcome in untreated subjects with mild hyperphenylalaninemia, PEDIAT RES, 49(4), 2001, pp. 532-536
Quality management in postoperative pain therapy
Authors: Meissner, W Ullrich, K Zwacka, S Schreiber, T Reinhart, K
Citation: W. Meissner et al., Quality management in postoperative pain therapy, ANAESTHESIS, 50(9), 2001, pp. 661
Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfalls
Authors: Das, AM Fingerhut, R Wanders, RJA Ullrich, K
Citation: Am. Das et al., Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfalls, EUR J PED, 159(4), 2000, pp. 243-246
In vivo proton magnetic resonance spectroscopy in phenylketonuria
Authors: Moller, HE Ullrich, K Weglage, J
Citation: He. Moller et al., In vivo proton magnetic resonance spectroscopy in phenylketonuria, EUR J PED, 159, 2000, pp. S121-S125
The international collaborative study of maternal phenylketonuria: status report 1998
Authors: Koch, R Friedman, E Azen, C Hanley, W Levy, H Matalon, R Rouse, B Trefz, F Waisbren, S Michals-Matalon, K Acosta, P Guttler, F Ullrich, K Platt, L de la Cruz, F
Citation: R. Koch et al., The international collaborative study of maternal phenylketonuria: status report 1998, EUR J PED, 159, 2000, pp. S156-S160
Upregulation of respiratory chain enzymes in guanidinoacetate methyltransferase deficiency
Authors: Das, AM Ullrich, K Isbrandt, D
Citation: Am. Das et al., Upregulation of respiratory chain enzymes in guanidinoacetate methyltransferase deficiency, J INH MET D, 23(4), 2000, pp. 375-377
Successful treatment of Mycobacterium avium osteomyelitis and arthritis ina non-immunocompromised child
Authors: Frosch, M Roth, J Ullrich, K Harms, E
Citation: M. Frosch et al., Successful treatment of Mycobacterium avium osteomyelitis and arthritis ina non-immunocompromised child, SC J IN DIS, 32(3), 2000, pp. 328-329
Neutropenia, neutrophil dysfunction, and inflammatory bowel disease in glycogen storage disease type Ib: Results of the European Study on Glycogen Storage Disease Type I
Authors: Visser, G Rake, JP Fernandes, J Labrune, P Leonard, JV Moses, S Ullrich, K Smit, GPA
Citation: G. Visser et al., Neutropenia, neutrophil dysfunction, and inflammatory bowel disease in glycogen storage disease type Ib: Results of the European Study on Glycogen Storage Disease Type I, J PEDIAT, 137(2), 2000, pp. 187-191
The international collaborative study of maternal phenylketonuria status report 1998
Authors: Koch, R Friedman, E Azen, C Hanley, W Levy, H Matalon, R Rouse, B Trefz, F Waisbren, S Michals-Matalon, K Acosta, P Guttler, F Ullrich, K Platt, L de la Cruz, F
Citation: R. Koch et al., The international collaborative study of maternal phenylketonuria status report 1998, MENT RET D, 5(2), 1999, pp. 117-121
The course of fibrinolytic proteins in children with malignant bone tumours
Authors: Nowak-Gottl, U Munchow, N Klippel, U Paulussen, M Bielack, S Ullrich, K Ehrenforth, S
Citation: U. Nowak-gottl et al., The course of fibrinolytic proteins in children with malignant bone tumours, EUR J PED, 158, 1999, pp. S151-S153
Indication for liver transplantation in metabolic disorders - Preface
Authors: Burdelski, M Ullrich, K
Citation: M. Burdelski et K. Ullrich, Indication for liver transplantation in metabolic disorders - Preface, EUR J PED, 158, 1999, pp. S33-S33
Liver transplantation in metabolic disorders: summary of the general discussion
Authors: Burdelski, M Ullrich, K
Citation: M. Burdelski et K. Ullrich, Liver transplantation in metabolic disorders: summary of the general discussion, EUR J PED, 158, 1999, pp. S95-S96
Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997
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
Regression of neuropsychological deficits in early-treated phenylketonurics during adolescence
Authors: Weglage, J Pietsch, M Denecke, J Sprinz, A Feldmann, R Grenzebach, M Ullrich, K
Citation: J. Weglage et al., Regression of neuropsychological deficits in early-treated phenylketonurics during adolescence, J INH MET D, 22(6), 1999, pp. 693-705
Glutaric aciduria type I: Pathomechanisms of neurodegeneration
Authors: Ullrich, K Flott-Rahmel, B Schluff, P Musshoff, U Das, A Lucke, T Steinfeld, R Christensen, E Jakobs, C Ludolph, A Neu, A Roper, R
Citation: K. Ullrich et al., Glutaric aciduria type I: Pathomechanisms of neurodegeneration, J INH MET D, 22(4), 1999, pp. 392-403
Risultati: 1-18 |