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Gessler, Peter; Buchal, Peter; Schwenk, Hans U; Wermuth, Bendicht (2010). Favourable long-term outcome after immediate treatment of neonatal hyperammonemia due to N-acetylglutamate synthase deficiency. European journal of pediatrics, 169(2), pp. 197-9. Berlin: Springer 10.1007/s00431-009-1006-0
Numata, S; Koda, Y; Ihara, K; Sawada, T; Okano, Y; Matsuura, T; Endo, F; Yoo, HW; Arranz, JA; Rubio, V; Wermuth, B; Mew, NA; Tuchman, M; Pinner, JR; Kirk, EP; Yoshino, M (2010). Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations. Journal of human genetics, 55(1), pp. 18-22. Avenel, N.J.: Nature Publishing Group 10.1038/jhg.2009.113
Wallemacq, P; Maine, GT; Berg, K; Rosiere, T; Marquet, P; Aimo, G; Mengozzi, G; Young, J; Wonigeit, K; Kretschmer, R; Wermuth, B; Schmid, RW (2010). Multisite analytical evaluation of the Abbott ARCHITECT cyclosporine assay. Therapeutic drug monitoring, 32(2), pp. 145-151. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1097/FTD.0b013e3181d46386
Schild, Christof; Wermuth, Bendicht; Trapp-Chiappini, Daniela; Egger, Florence; Nuoffer, Jean-Marc (2008). Reliability of M protein quantification: comparison of two peak integration methods on Capillarys 2. Clinical chemistry and laboratory medicine, 46(6), pp. 876-877. Berlin: Walter de Gruyter 10.1515/CCLM.2008.146
Engel, Katharina; Nuoffer, Jean-Marc; Mühlhausen, Chris; Klaus, Vera; Largiadèr, Carlo R; Tsiakas, Konstantinos; Santer, René; Wermuth, Bendicht; Häberle, Johannes (2008). Analysis of mRNA transcripts improves the success rate of molecular genetic testing in OTC deficiency. Molecular genetics and metabolism, 94(3), pp. 292-7. Amsterdam: Elsevier 10.1016/j.ymgme.2008.03.009
Sciotti, Michel A; Tam, Steven; Wermuth, Bendicht; Baker, Michael E (2006). Differences in catalytic activity between rat testicular and ovarian carbonyl reductases are due to two amino acids. FEBS letters, 580(1), pp. 67-71. Amsterdam: Elsevier 10.1016/j.febslet.2005.11.049
Serra, Andreas L; Klein, Maja; Nitsch, Dorothea; Dürr, Daniel; Wermuth, Bendicht; Frey, Felix J (2006). A puzzling case of high serum creatinine in a healthy woman. Nephrology, dialysis, transplantation, 21(5), pp. 1456-7. Oxford: Oxford University Press 10.1093/ndt/gfi343
Azevedo, L; Soares, P A; Quental, R; Vilarinho, L; Teles, E L; Martins, E; Diogo, L; Garcia, P; Cenni, B; Wermuth, B; Amorim, A (2006). Mutational spectrum and linkage disequilibrium patterns at the ornithine transcarbamylase gene (OTC). Annals of human genetics, 70(Pt 6), pp. 797-801. Oxford: Wiley-Blackwell 10.1111/j.1469-1809.2006.00283.x
von Vigier, Rodo O.; Truttmann, Anita C.; Zindler‐Schmocker, Karin; Bettinelli, Alberto; Casaulta Aebischer, Carmen; Wermuth, Bendicht; Bianchetti, Mario G. (2000). Aminoglycosides and renal magnesium homeostasis in humans. Nephrology, dialysis, transplantation, 15(6), pp. 822-826. Oxford University Press 10.1093/ndt/15.6.822
Pedrozzi, Nicola E.; Truttmann, Anita C.; Faraone, Rita; Descoeudres, Claude E.; Wermuth, Bendicht; Lüthy, Christa M.; Nuoffer, Jean-Marc; Frey, Felix; Bianchetti, Mario Giovanni (1998). Circulating Ionized and Total Magnesium in End-Stage Kidney Disease. Nephron, 79(3), pp. 288-292. Karger 10.1159/000045051
Vella, S.; Steiner, F.; Schlumbom, V.; Zurbrügg, R.; Wiesmann, U. N.; Schaffner, T.; Wermuth, B. (1997). Mutation of ornithine transcarbamylase (H136R) in a girl with severe intermittent orotic aciduria but normal enzyme activity. Journal of inherited metabolic disease, 20(4), pp. 517-524. Springer 10.1023/A:1005397329395
