Clinical Guide and Update on Porphyrias von Stölzel, Ulrich, Doss, Manfred O., Schuppan, Detlef

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Hereditary coproporphyria in Germany: clinical-biochemical studies in 53 patients von Kühnel, Alexandra, Gross, Ulrich, Doss, Manfred O

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Singlet Oxygen Inactivates Fibrinogen, Factor V, Factor VIII, Factor X, and Platelet Aggregation of Human Blood von Stief, Thomas W, Kurz, Jürgen, Doss, Manfred O, Fareed, Jawed

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ALCOHOL AND PORPHYRIN METABOLISM von Doss, Manfred O., Kühnel, Alexandra, Gross, Ulrich

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Regulation of Pseudomonas aeruginosa hemF and hemN by the dual action of the redox response regulators Anr and Dnr von Rompf, Alexandra, Hungerer, Christoph, Hoffmann, Tamara, Lindenmeyer, Maja, Römling, Ute, Groß, Ulrich, Doss, Manfred O., Arai, Hiroyuki, Igarashi, Yasuo, Jahn, Dieter

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Highly heterogeneous nature of δ-aminolevulinate dehydratase (ALAD) deficiencies in ALAD porphyria von Maruno, Motoyoshi, Furuyama, Kazumichi, Akagi, Reiko, Horie, Yutaka, Meguro, Kuniaki, Garbaczewski, Luba, Chiorazzi, Nicholas, Doss, Manfred O., Hassoun, Alexandre, Mercelis, Rudolf, Verstraeten, Luc, Harper, Pauline, Floderus, Ylva, Thunell, Stig, Sassa, Shigeru

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Variegate porphyria with coexistent decrease in porphobilinogen deaminase activity von WEINLICH, Georg, DOSS, Manfred O, SEPP, Norbert, FRITSCH, Peter

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Hepatobiliary implications and complications in protoporphyria, a 20-year study von Doss, Manfred O., Frank, Margareta

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Singlet oxygen (1O2) Inactivates Plasmatic Free and Complexed α2-Macroglobulin von Stief, Thomas W, Kropf, Jürgen, Kretschmer, Volker, Doss, Manfred O, Fareed, Jawed

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Thrombin converts singlet oxygen (1O2)-oxidized fibrinogen into a soluble t-PA cofactor A new method for preparing a stimulator for functional t-PA assays von STIEF, Thomas W, KRETSCHMER, Volker, KOSCHE, Britta, DOSS, Manfred O, RENZ, Harald

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A Simple Screening Assay for Certain Fibrinolysis Parameters (FIPA) von Stief, Thomas W, Hinz, Frauke, Kurz, Jürgen, Doss, Manfred O, Kretschmer, Volker

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Hemochromatosis (HFE) Gene Mutations and Response to Chloroquine in Porphyria Cutanea Tarda von Stölzel, Ulrich, Köstler, Erich, Schuppan, Detlef, Richter, Matthias, Wollina, Uwe, Doss, Manfred O, Wittekind, Christian, Tannapfel, Andrea

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Relevance of urinary coproporphyrin isomers in hereditary hyperbilirubinemias von Frank, Margareta, Doss, Manfred O.

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Low prevalence of hepatitis c virus infection in porphyria cutanea tarda in Germany von Stolzel, Ulrich, Kostler, Erich, Koszka, Christiane, Stoffler-Meilicke, Maricka, Schuppan, Detlef, Somasundaram, Rajan, Doss, Manfred O., Habermehl, Karl O., Riecken, Ernst O.

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Novel molecular defects of the δ‐aminolevulinate dehydratase gene in a patient with inherited acute hepatic porphyria von Akagi, Reiko, Shimizu, Ryo, Furuyama, Kazumichi, Doss, Manfred O., Sassa, Shigeru

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Investigations on the formation of urinary coproporphyrin isomers I–IV in 5-aminolevulinic acid dehydratase deficiency porphyria, acute lead intoxication and after oral 5-aminolevu... von Jacob, Karl, Egeler, Emil, Groß, Ulrich, Doss, ManfredO

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Clinical impact of heterozygosity for the C282Y and H63D mutation of the hemochromatosis (HFE) gene in chloroquine treated patients with porphyria cutanea tarda (PCT) in Germany von Stoelzel, Ulrich, Tannapfel, Andrea, Schuppan, Detlef, Richter, Matthias, Keim, Volker, Doss, Manfred O., Melz, Steffi, Koestler, Erich

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Porphyrinurias and Occupational Disease von DOSS, MANFRED O.

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Porphyrinurias and Occupational Diseasea von DOSS, MANFRED O.

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Hepatische Porphyrien von Doss, Manfred O.

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