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Annals of Clinical Research|January 1, 1976
Hexachlorobenzene porphyria in rats as a model for human chronic hepatic porphyriasM Doss, E Schermuly, G KossInternational Archives of Occupational and Environmental Health|January 1, 1984
Lead poisoning in inherited delta-aminolevulinic acid dehydratase deficiencyM Doss, F Laubenthal, M StoepplerZeitschrift Fur Naturforschung. Section C, Biosciences|May 1, 1975
Over-production of porphyrins and heme in heterotrophic bacteriaW K Philipp-Dormston, M DossPlos Biology|August 23, 2024
A somatic view of the genomic impact of mitochondrial endosymbiosisRose M Doss, Martin W BreussKlinische Wochenschrift|July 15, 1983
Porphobilinogen-synthase (delta-aminolevulinic acid dehydratase) deficiency in bone marrow cells of two patients with porphobilinogen-synthase defect acute porphyriaM Doss, R V Tiepermann, J SchneiderMedizinische Klinik|August 4, 1978
[Disorder of porphyrin metabolism in thallium intoxication (author's transl)]N Graben, M Doss, H A KlöppelHoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|August 1, 1980
Uroporphyrinogen decarboxylase deficiency in experimental chronic hepatic porphyriaR von Tiepermann, G Koss, M DossKlinische Wochenschrift|February 15, 1984
Vinyl chloride-induced hepatic coproporphyrinuria with transition to chronic hepatic porphyriaM Doss, C E Lange, G VeltmanEuropean Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|September 28, 2001
Long term follow up of left ventricular function after repair of left ventricular aneurysm. A comparison of linear closure versus patch plastyM Doss, S Martens, S Sayour, et al.Clinical Genetics|September 1, 1986
delta-Aminolevulinic acid dehydrase (porphobilinogen synthase) in two families with inherited enzyme deficiencyM Doss, H G Benkmann, H W GoeddePageof 11