Thomas Matthes
Department of Internal Medicine
Unit of Clinical Hematology
University Hospital
Geneva
Switzerland
Name/email consistency: high
- Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion. Matthes, T., Rustin, P., Trachsel, H., Darbellay, R., Costaridou, S., Xaidara, A., Rideau, A., Beris, P. Eur. J. Haematol. (2006)
- Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5'-UTR of the HAMP gene. Matthes, T., Aguilar-Martinez, P., Pizzi-Bosman, L., Darbellay, R., Rubbia-Brandt, L., Giostra, E., Michel, M., Ganz, T., Beris, P. Blood (2004)
- Acquired and transient RBC CD55 deficiency (Inab phenotype) and anti-IFC. Matthes, T., Tullen, E., Poole, J., Banks, J., Nagy, M., Stelling, M.J., Boehlen, F., Michel, M., Beris, P., Hustinx, H., Crew, V., Daniels, G. Transfusion (2002)
- Cytomegalovirus colitis--a severe complication after standard chemotherapy. Matthes, T., Kaiser, L., Weber, D., Kurt, A.M., Dietrich, P.Y. Acta. Oncol (2002)
- Increased apoptosis in acquired sideroblastic anaemia. Matthes, T.W., Meyer, G., Samii, K., Beris, P. Br. J. Haematol. (2000)