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Results:
1-9
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Results: 9
Authors:
Burlina, AB
Ogier, H
Korall, H
Trefz, FK
Citation: Ab. Burlina et al., Long-term treatment with sodium phenylbutyrate in ornithine transcarbamylase-deficient patients, MOL GEN MET, 72(4), 2001, pp. 351-355
Authors:
Trefz, FK
Aulela-Scholz, C
Blau, N
Citation: Fk. Trefz et al., Successful treatment of phenylketonuria with tetrahydrobiopterin, EUR J PED, 160(5), 2001, pp. 315-315
Authors:
Tomaske, M
Bosk, A
Heinemann, MK
Sieverding, L
Baumgartner, ER
Fowler, B
Trefz, FK
Citation: M. Tomaske et al., CASE REPORT: CblC/D defect combined with haemodynamically highly relevant VSD, J INH MET D, 24(4), 2001, pp. 511-512
Authors:
Heinemann, MK
Tomaske, M
Trefz, FK
Bosk, A
Baden, W
Ziemer, G
Citation: Mk. Heinemann et al., Ventricular septal defect closure in a neonate with combined methylmalonicaciduria/homocystinuria, ANN THORAC, 72(4), 2001, pp. 1391-1392
Authors:
Spiekerkotter, U
Schwahn, B
Korall, H
Trefz, FK
Andresen, BS
Wendel, U
Citation: U. Spiekerkotter et al., Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: monitoring of treatment by carnitine/acylcarnitine analysis in blood spots, ACT PAEDIAT, 89(4), 2000, pp. 492-495
Authors:
Trefz, FK
Cipcic-Schmidt, S
Koch, R
Citation: Fk. Trefz et al., Final intelligence in late treated patients with phenylketonuria, EUR J PED, 159, 2000, pp. S145-S148
Authors:
Mau, UA
Backsch, C
Schaudt, H
Trefz, FK
Kaiser, P
Citation: Ua. Mau et al., Three-year-old girl with partial trisomy 4p and partial monosomy 8p with resemblance to Brachmann-de Lange syndrome - Another locus for Brachmann-de Lange syndrome on 4p?, AM J MED G, 91(3), 2000, pp. 180-184
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:
Matern, D
Strauss, AW
Hillman, SL
Mayatepek, E
Millington, DS
Trefz, FK
Citation: D. Matern et al., Diagnosis of mitochondrial trifunctional protein deficiency in a blood spot from the newborn screening card by tandem mass spectrometry and DNA analysis, PEDIAT RES, 46(1), 1999, pp. 45-49
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