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The 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 DossZeitschrift Fur Klinische Chemie Und Klinische Biochemie|July 1, 1975
Separation of the coprophorphyrin isomers I and III by thin-layer chromatographyE Schermuly, M DossAnnals of Clinical Research|January 1, 1976
Porphyrin biosynthesis from ALA and PBG by human erythrocytes in porphyrin disorders. Kinetic studies of the isomer series I and IIIE Schermuly, M DossDeutsche Medizinische Wochenschrift (1946)|February 20, 1981
[Chronic hepatic porphyria with uroporphyrinogen decarboxylase defect in four generations (author's transl)]P A Lehr, M DossDeutsche Medizinische Wochenschrift (1946)|May 21, 1982
[Hereditary coproporphyria (author's transl)]K H Pflüger, M DossBlut|August 1, 1982
Acute lead poisoning in inherited porphobilinogen synthase (delta-aminolevulinic acid dehydrase) deficiencyM Doss, W A MüllerJournal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|September 1, 1978
[Uroporphyrinogen decarboxylase in erythrocytes: studies on the primary genetic enzyme defect in chronic hepatic porphyria (author's transl)]R von Tiepermann, M DossJournal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|February 1, 1978
[Uroporphyrinogen synthase in erythrocytes in acute intermittent porphyria: new pathobiochemical aspects (author's transl)]M Doss, R von TiepermannPediatric Clinics of North America|November 28, 2017
Open Up and Let Us In: An Interprofessional Approach to Oral HealthMona M Sedrak, Laura M DossPageof 11