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Results: 1-7 |
Results: 7

Authors: Feix, A Fritsche-Polanz, R Kletzmayr, J Vychytil, A Horl, WH Sunder-Plassmann, G Fodinger, M
Citation: A. Feix et al., Increased prevalence of combined MTR and MTHFR genotypes among individualswith severely elevated total homocysteine plasma levels, AM J KIDNEY, 38(5), 2001, pp. 956-964

Authors: Jordan, JH Fritsche-Polanz, R Sperr, WR Mitterbauer, G Fodinger, M Schernthaner, GH Bankl, HC Gebhart, W Chott, A Lechner, K Valent, P
Citation: Jh. Jordan et al., A case of 'smouldering' mastocytosis with high mast cell burden, monoclonal myeloid cells, and C-KIT mutation Asp-816-Val, LEUK RES, 25(7), 2001, pp. 627-634

Authors: Fritsche-Polanz, R Jordan, JH Feix, A Sperr, WR Sunder-Plassmann, G Valent, P Fodinger, M
Citation: R. Fritsche-polanz et al., Mutation analysis of C-KIT in patients with myelodysplastic syndromes without mastocytosis and cases of systemic mastocytosis, BR J HAEM, 113(2), 2001, pp. 357-364

Authors: Fodinger, M Fritsche-Polanz, R Buchmayer, H Skoupy, S Sengoelge, G Horl, WH Sunder-Plassmann, G
Citation: M. Fodinger et al., Erythropoietin-inducible immediate-early genes in human vascular endothelial cells, J INVES MED, 48(2), 2000, pp. 137-149

Authors: Fodinger, M Fritsche-Polanz, R Schedler, D Horl, WH Sunder-Plassmann, G
Citation: M. Fodinger et al., Two novel mutations in the beta subunit of the human epithelial sodium channel, KIDNEY INT, 55(6), 1999, pp. 2530-2531

Authors: Fodinger, M Schedler, D Fritsche-Polanz, R Horl, WH Sunder-Plassmann, G
Citation: M. Fodinger et al., Molecular analysis of the carboxy terminus of the beta and gamma subunits of the epithelial sodium channel in patients with end-stage renal disease, NEPHRON, 81(4), 1999, pp. 381-386

Authors: Sperr, WR Walchshofer, S Horny, HP Fodinger, M Simonitsch, I Fritsche-Polanz, R Schwarzinger, I Tschachler, E Sillaber, C Hagen, W Geissler, K Chott, A Lechner, K Valent, P
Citation: Wr. Sperr et al., Systemic mastocytosis associated with acute myeloid leukaemia: report of two cases and detection of the c-kit mutation Asp-816 to Val, BR J HAEM, 103(3), 1998, pp. 740-749
Risultati: 1-7 |