Friedrich Sandhofer

Corresponding Member of the Division of Mathematics and the Natural Sciences in Austria since 1999
- Landesklinik für Innere Medizin I
Contact:
Research Areas:
- Clinical Medicine
- Medical molecular biology
- Lipidomics research
- Diabetology
- Hepatology
Selected Memberships:
- New York Academy of Sciences
- Academia Scientiarum et Artium Europaea
Selected Prizes:
- Kardinal-Innitzer-Preis
Selected Publications:
- Weitgasser, R.; Spitzer, D.; Kartnig, I.; Staudach, A.; Sandhofer, F. (2000) Association of HELLP syndrome with autoimmune antibodies and glucose intolerance. Diabetes Care, Bd. 23, S. 786.
- Datz, C.; Lalloz, M. R .A.; Vogel, W.; Graziadei, I.; Hackl, F. et al. [..] (1997) Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis. Journal of Hepatology, Bd. 27, S. 773.
- Miesenböck, G.; Hölzl, B.; Föger, B.; Brandstätter, E.; Paulweber, B. et al. [..] (1993) Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities. Journal of Clinical Investigation, Bd. 91, S. 448.
- Paulweber, B.; Sandhofer, F.; Levy-Wilson, B. (1993) The mechanism by which the human apolipoprotein B gene reducer operates involves blocking of transcriptional activation by hepatocyte nuclear factor 3. Molecular and Cell Biolgy, Bd. 13, S. 1534.
- Krempler, F.; Kostner, G. M.; Bolzano, K.; Sandhofer, F. (1980) Turnover of lipoprotein(a) in man. Journal of Clinical Investigation, Bd. 65, S. 1483.