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Number of items: 6.

Häberle, Johannes; Rubio, V (2016). Disorders of the urea cycle and related enzymes. In: Saudubray, J M; Baumgartner, M; Walter, J H. Inborn metabolic diseases. Berlin Heidelberg: Springer Verlag, 295-308.

Baumgartner, M R; Suormala, T (2012). Biotin-responsive disorders. In: Saudubray, J M; van den Berghe, G; Walter, J H. Inborn metabolic diseases: diagnosis and treatment (5th ed.). Berlin, DE: Springer, 375-384.

Steinmann, B; Santer, R (2012). Disorders of Fructose Metabolism. In: Saudubray, G; van den Berghe, G; Walter, J H. Inborn Metabolic Diseases - Diagnosis and Treatment. Berlin: Springer, 157-165.

Baumgartner, M R; Valle, D (2012). Disorders of ornithine metabolism. In: Saudubray, J M; van den Berghe, G; Walter, J H. Inborn metabolic diseases: diagnosis and treatment (5th ed.). Berlin, DE: Springer, 323-332.

Hörster, F; Garbade, S F; Zwickler, T; Aydin, H I; Bodamer, O A; Burlina, A B; Das, A M; De Klerk, J B; Dionisi-Vici, C; Geb, S; Gökcay, G; Guffon, N; Maier, E M; Morava, E; Walter, J H; Schwan, B; Wijburg, F A; Lindner, M; Grünewald, S; Baumgartner, M R; Kölker, S (2009). Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters. Journal of Inherited Metabolic Disease, 32(5):630-639.

Zwickler, T; Lindner, M; Aydin, H I; Baumgartner, M R; Bodamer, O A; Burlina, A B; Das, A M; DeKlerk, J B C; Gökcay, G; Grünewald, S; Guffon, N; Maier, E M; Morava, E; Geb, S; Schwahn, B; Walter, J H; Wendel, U; Wijburg, F A; Müller, E; Kölker, S; Hörster, F (2008). Diagnostic work-up and management of patients with isolated methylmalonic acidurias in European metabolic centres. Journal of Inherited Metabolic Disease, 31(3):361-367.

This list was generated on Thu Dec 14 16:55:52 2017 CET.