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Results:
1-13
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Results: 13
Authors:
Plochl, W
Plochl, E
Pokorny, H
Kozek-Langenecker, S
Zacherl, J
Stockler-Ipsiroglu, S
Wermuth, B
Spiss, CK
Muhlbacher, F
Citation: W. Plochl et al., Multiorgan donation from a donor with unrecognized ornithine transcarbamylase deficiency, TRANSPLAN I, 14(3), 2001, pp. 196-201
Authors:
Rapp, B
Haberle, J
Linnebank, M
Wermuth, B
Marquardt, T
Harms, E
Koch, HG
Citation: B. Rapp et al., Genetic analysis of carbamoylphosphate synthetase I and ornithine transcarbamylase deficiency using fibroblasts, EUR J PED, 160(5), 2001, pp. 283-287
Authors:
Plochl, E
Plochl, W
Wermuth, B
Roscher, AA
Citation: E. Plochl et al., Variants of inborn errors of metabolism with late onset but nevertheless life threatening course, KLIN PADIAT, 213(5), 2001, pp. 261-265
Authors:
Ploechl, E
Ploechl, W
Stoeckler-Ipsiroglu, S
Pokorny, H
Wermuth, B
Citation: E. Ploechl et al., Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codon, CLIN GENET, 59(2), 2001, pp. 111-114
Authors:
Sciotti, MA
Wermuth, B
Citation: Ma. Sciotti et B. Wermuth, Coenzyme specificity of human monomeric carbonyl reductase: contribution of Lys-15, Ala-37 and Arg-38, CHEM-BIO IN, 130(1-3), 2001, pp. 871-878
Authors:
von Vigier, RO
Truttmann, AC
Zindler-Schmocker, K
Bettinelli, A
Aebischer, CC
Wermuth, B
Bianchetti, MG
Citation: Ro. Von Vigier et al., Aminoglycosides and renal magnesium homeostasis in humans, NEPH DIAL T, 15(6), 2000, pp. 822-826
Authors:
Sciotti, MA
Nakajin, S
Wermuth, B
Baker, ME
Citation: Ma. Sciotti et al., Mutation of threonine-241 to proline eliminates autocatalytic modificationof human carbonyl reductase, BIOCHEM J, 350, 2000, pp. 89-92
Authors:
van Bakel, MME
Printzen, G
Wermuth, B
Wiesmann, UN
Citation: Mme. Van Bakel et al., Antioxidant and thyroid hormone status in selenium-deficient phenylketonuric and hyperphenylalaninemic patients, AM J CLIN N, 72(4), 2000, pp. 976-981
Authors:
Vannini, SDP
Mazzola, BL
Rodoni, L
Truttmann, AC
Wermuth, B
Bianchetti, MG
Ferrari, P
Citation: Sdp. Vannini et al., Permanently reduced plasma ionized magnesium among renal transplant recipients on cyclosporine, TRANSPLAN I, 12(4), 1999, pp. 244-249
Authors:
Forget, PP
van Oosterhout, M
Bakker, JA
Wermuth, B
Vles, JSH
Spaapen, LJM
Citation: Pp. Forget et al., Partial N-acetyl-glutamate synthetase deficiency masquerading as a valproic acid-induced Reye-like syndrome, ACT PAEDIAT, 88(12), 1999, pp. 1409-1411
Authors:
Schaller, M
Schaffhauser, M
Sans, N
Wermuth, B
Citation: M. Schaller et al., Cloning and expression of succinic semialdehyde reductase from human brain- Identity with aflatoxin B-1 aldehyde reductase, EUR J BIOCH, 265(3), 1999, pp. 1056-1060
Authors:
Tinguely, JN
Wermuth, B
Citation: Jn. Tinguely et B. Wermuth, Identification of the reactive cysteine residue (Cys227) in human carbonylreductase, EUR J BIOCH, 260(1), 1999, pp. 9-14
Authors:
Plecko, B
Erwa, W
Wermuth, B
Citation: B. Plecko et al., Partial N acetylglutamate synthetase deficiency in a 13-year-old girl: diagnosis and response to treatment with N-carbamylglutamate, EUR J PED, 157(12), 1998, pp. 996-998
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1-13
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