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Human Toxicology|May 1, 1985
Acute lead intoxication due to intravenous injectionF Sixel-Dietrich, M Doss, C H Pfeil, et al.Archives of Dermatological Research|January 1, 1985
Hereditary uroporphyrinogen-decarboxylase deficiency predisposing porphyria cutanea tarda (chronic hepatic porphyria) in females after oral contraceptive medicationF Sixel-Dietrich, M DossJournal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|September 1, 1985
"Glucose effect" and rate limiting function of uroporphyrinogen synthase on porphyrin metabolism in hepatocyte culture: relationship with human acute hepatic porphyriasM Doss, F Sixel-Dietrich, F VerspohlHormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|July 1, 1985
Hyperinsulinemia in acute intermittent porphyriaF Sixel-Dietrich, F Verspohl, M DossKlinische Wochenschrift|June 15, 1982
Persistent protoporphyrinemia in hereditary porphobilinogen synthase (delta-aminolevulinic acid dehydrase) deficiency under low lead exposure. A new molecular basis for the pathogenesis of lead intoxicationM Doss, U Becker, F Sixel, et al.The Thoracic and Cardiovascular Surgeon|February 27, 1998
Unusually high uptake of fluoro-2-deoxy-D-glucose on PET scanning of a benign paravertebral massM DossLeber, Magen, Darm|October 1, 1978
[Alcohol-induced changes of porphyrin metabolism (author's transl)]M DossMMW, Munchener Medizinische Wochenschrift|November 16, 1979
[Diagnosis and differential diagnosis of acute hepatic prophyrias (author's transl)]M DossThe Journal of Cardiovascular Surgery|November 8, 2001
Fate of bypass grafts onto totally occluded coronary arteriesM Doss, W HemmerHuman Genetics|January 1, 1981
Hereditary prophobilinogen synthase deficiency in human associated with acute hepatic porphyriaA Brandt, M DossPageof 10