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Number of items: 18.

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.

Fiaschetti, G; Abela, L; Nonoguchi, N; Dubuc, A M; Remke, M; Boro, A; Grunder, E; Siler, U; Ohgaki, H; Taylor, M D; Baumgartner, M; Shalaby, T; Grotzer, M A (2014). Epigenetic silencing of miRNA-9 is associated with HES1 oncogenic activity and poor prognosis of medulloblastoma. British Journal of Cancer, 110(3):636-647.

Sass, Jörn Oliver; Baumgartner, M (2013). Inborn errors of cobalamin absorption, transport and metabolism. In: ACTA Pediátrica Española, Congreso nacional de Errores Congénitos del Metabolismo, 1 September 2013 - 2 September 2013, 18-21.

Baumgartner, M; Brugnera, E; Sydler, T; Bürgi, E; Hässig, M; Sidler, X (2012). Risk factors causing postweaning multisystemic wasting syndrome (PMWS) onset in Swiss pig farms. Schweizer Archiv für Tierheilkunde, 154(10):429-436.

Keller, H; Baumgartner, M; Beywl, W; Claude, A; Mudry, A; Widmer, T (2011). Zur Einordnung von Q-Labels im Bildungsbereich. Bern: Schweizerische Zentralstelle für die Weiterbildung der Mittelschullehrpersonen.

Rohrbach, M; Vandersteen, A; Yiş, U; Serdaroglu, G; Ataman, E; Chopra, M; Garcia, S; Jones, K; Kariminejad, A; Kraenzlin, M; Marcelis, C; Baumgartner, M; Giunta, C (2011). Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation. Orphanet Journal of Rare Diseases, 6:46.

Juras, K; Fumić, K; Izaković, S; Puseljić, S; Culić, V; Galić, S; Buljević, A D; Benjak, V; Colić, A; Frković, S H; Maradin, M; Sarnavka, V; Bilić, K; Baumgartner, M; Barić, I (2011). Manjak vitamina B12 u djece - podcijenjena opasnost u svjetlu spoznaja. Lijec̆nic̆ki vjesnik, 133(1-2):39-50.

Kretz, R; Bozorgmehr, B; Kariminejad, M H; Rohrbach, M; Hausser, I; Baumer, A; Baumgartner, M; Giunta, C; Kariminejad, A; Häberle, J (2011). Defect in proline synthesis: pyrroline-5-carboxylate reductase 1 deficiency leads to a complex clinical phenotype with collagen and elastin abnormalities. Journal of Inherited Metabolic Disease, 34(3):731-739.

Mortezavi, A; Hermanns, T; Seifert, H H; Baumgartner, M; Provenzano, M; Sulser, T; Burger, M; Montani, M; Ikenberg, K; Hofstaedter, F; Hartmann, A; Jaggi, R; Moch, H; Kristiansen, G; Wild, P J (2011). KPNA2 expression is an independent adverse predictor of biochemical recurrence after radical prostatectomy. Clinical Cancer Research, 17(5):1111-1121.

Baumgartner, M. Risikofaktoren in PMWS-Betrieben (Postweaning Multisystemic Wasting Syndrom) in Schweizer Schweinezuchtbetrieben. 2011, University of Zurich, Vetsuisse Faculty.

Schmitt, B; Baumgartner, M; Mills, P B; Clayton, P T; Jakobs, C; Keller, E; Wohlrab, G (2010). Seizures and paroxysmal events: symptoms pointing to the diagnosis of pyridoxine-dependent epilepsy and pyridoxine phosphate oxidase deficiency. Developmental Medicine and Child Neurology, 52(7):e133-e142.

Feicke, A; Baumgartner, M; Talimi, S; Schmid, D M; Seifert, H H; Müntener, M; Fatzer, M; Sulser, T; Strebel, R T (2009). Robotic-assisted laparoscopic extended pelvic lymph node dissection for prostate cancer: surgical technique and experience with the first 99 cases. European Urology, 55(4):876-884.

Sutter, R; Killer, H E; Bilz, S; Baumgartner, M; Ott, H W; Steck, A J; Renaud, S (2009). Cerebral edema and intracranial hypertension in an adult with maple syrup urine disease. European Journal of Neurology, 16(3):e45-e46.

Ajdacic-Gross, V; Lauber, C; Baumgartner, M; Malti, T; Rössler, W (2009). In-patient suicide – a 13-year assessment. Acta Psychiatrica Scandinavica, 120(1):71-75.

Rutsch, F; Gailus, S; Miousse, I R; Suormala, T; Sagné, C; Toliat, M R; Nürnberg, G; Wittkampf, T; Buers, I; Sharifi, A; Stucki, M; Becker, C; Baumgartner, M; Robenek, H; Marquardt, T; Höhne, W; Gasnier, B; Rosenblatt, D S; Fowler, B; Nürnberg, P (2009). Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism. Nature Genetics, 41(2):234-239.

Paesold-Burda, P; Maag, C; Troxler, H; Foulquier, F; Kleinert, P; Schnabel, S; Baumgartner, M; Hennet, T (2009). Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation. Human Molecular Genetics, 18(22):4350-4356.

Barben, J; Torresani, T; Schöni, M H; Gallati, S; Baumgartner, M (2008). Neugeborenen-Screening auf zystische Fibrose - bald auch in der Schweiz? Swiss Medical Forum, 8(45):873-875.

Kupper, J; Baumgartner, M; Bacciarini, L N; Hoop, R; Kupferschmidt, H; Naegeli, H (2007). Carbofuran-Vergiftung bei wildlebenden Stockenten. Schweizer Archiv für Tierheilkunde, 149(11):517-520.

This list was generated on Tue Jul 25 09:03:23 2017 CEST.