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The third case of Doss porphyria (δ‐amino‐levulinic acid dehydratase deficiency) in Germany

Journal of inherited metabolic disease, 2004-07, Vol.27 (4), p.529-536

2004

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Erythropoietic and hepatic porphyrias

Journal of inherited metabolic disease, 2000-11, Vol.23 (7), p.641-661

2000

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ALCOHOL AND PORPHYRIN METABOLISM

Alcohol and alcoholism (Oxford), 2000-03, Vol.35 (2), p.109-125

2000

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Hepatic complications of erythropoietic protoporphyria

Photodermatology, photoimmunology & photomedicine, 1998-04, Vol.14 (2), p.52-57

1998

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Biochemical compared to molecular diagnosis in acute intermittent porphyria

Journal of inherited metabolic disease, 2006-02, Vol.29 (1), p.157-161

2006

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A molecular, enzymatic and clinical study in a family with hereditary coproporphyria

Journal of inherited metabolic disease, 2002-06, Vol.25 (4), p.279-286

2002

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Studies on coproporphyrin isomers in urine and feces in the porphyrias

Clinica chimica acta, 1999-04, Vol.282 (1), p.45-58

1999

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A description of an HPLC assay of coproporphyrinogen III oxidase activity in mononuclear cells

Journal of inherited metabolic disease, 2003-01, Vol.26 (6), p.565-570

2003

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Survival of two patients with severe δ‐aminolaevulinic acid dehydratase deficiency porphyria

Journal of inherited metabolic disease, 2001-02, Vol.24 (1), p.60-64

2001

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5-Aminolevulinic acid dehydratase deficiency porphyria: a twenty-year clinical and biochemical follow-up

Clinical chemistry (Baltimore, Md.), 1998-09, Vol.44 (9), p.1892-1896

1998

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Novel molecular defects of the δ‐aminolevulinate dehydratase gene in a patient with inherited acute hepatic porphyria

Hepatology (Baltimore, Md.), 2000-03, Vol.31 (3), p.704-708

2000

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Safe and probably safe drugs in acute hepatic porphyria

Cellular and molecular biology (Noisy-le-Grand, France), 2009-07, Vol.55 (2), p.147

2009

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Variegate porphyria with coexistent decrease in porphobilinogen deaminase activity

Acta dermato-venereologica, 2001-10, Vol.81 (5), p.356-359

2001

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Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria

Cellular and molecular biology (Noisy-le-Grand, France), 2002-02, Vol.48 (1), p.49

2002

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Porphyria cutanea tarda (chronische hepatische Porphyrie)

Deutsche medizinische Wochenschrift, 1995-10, Vol.120 (41), p.1405-1410

1995

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Haem arginate interferes with estimation of carcinoembryonic antigen

Annals of clinical biochemistry, 2001-05, Vol.38 (Pt 3), p.275-276

2001

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Interdependence between degree of porphyrin excess and disease severity in congenital erythropoietic porphyria (Günther's disease)

Archives of Dermatological Research, 1997-04, Vol.289 (5), p.272-276

1997

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A Simple Screening Assay for Certain Fibrinolysis Parameters (FIPA)

Thrombosis research, 2000-02, Vol.97 (4), p.231-237

2000

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Treatment of porphyria cutanea tarda by the effect of chloroquine on the liver

Skin pharmacology, 1995, Vol.8 (3), p.156-161

1995

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Hormonal Oral Contraceptives, Urinary Porphyrin Excretion and Porphyrias

Hormone and metabolic research, 1995-08, Vol.27 (8), p.379-383

1995

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Singlet Oxygen Inactivates Fibrinogen, Factor V, Factor VIII, Factor X, and Platelet Aggregation of Human Blood

Thrombosis research, 2000-03, Vol.97 (6), p.473-480

2000

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Hereditary coproporphyria in Germany: clinical-biochemical studies in 53 patients

Clinical biochemistry, 2000-08, Vol.33 (6), p.465-473

2000

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New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyria

Molecular and cellular probes, 1999-12, Vol.13 (6), p.443-447

1999

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Compound heterozygous hereditary coproporphyria with fluorescing teeth

Annals of clinical biochemistry, 1999-09, Vol.36 ( Pt 5) (5), p.680-682

1999

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Regulation of Pseudomonas aeruginosa hemF and hemN by the dual action of the redox response regulators Anr and Dnr

Molecular microbiology, 1998-08, Vol.29 (4), p.985-997

1998

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The third case of Doss porphyria (δ‐amino‐levulinic acid dehydratase deficiency) in Germany

Erythropoietic and hepatic porphyrias

ALCOHOL AND PORPHYRIN METABOLISM

Hepatic complications of erythropoietic protoporphyria

Biochemical compared to molecular diagnosis in acute intermittent porphyria

A molecular, enzymatic and clinical study in a family with hereditary coproporphyria

Studies on coproporphyrin isomers in urine and feces in the porphyrias

A description of an HPLC assay of coproporphyrinogen III oxidase activity in mononuclear cells

Survival of two patients with severe δ‐aminolaevulinic acid dehydratase deficiency porphyria

5-Aminolevulinic acid dehydratase deficiency porphyria: a twenty-year clinical and biochemical follow-up

Novel molecular defects of the δ‐aminolevulinate dehydratase gene in a patient with inherited acute hepatic porphyria

Safe and probably safe drugs in acute hepatic porphyria

Variegate porphyria with coexistent decrease in porphobilinogen deaminase activity

Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria

Porphyria cutanea tarda (chronische hepatische Porphyrie)

Haem arginate interferes with estimation of carcinoembryonic antigen

Interdependence between degree of porphyrin excess and disease severity in congenital erythropoietic porphyria (Günther's disease)

A Simple Screening Assay for Certain Fibrinolysis Parameters (FIPA)

Treatment of porphyria cutanea tarda by the effect of chloroquine on the liver

Hormonal Oral Contraceptives, Urinary Porphyrin Excretion and Porphyrias

Singlet Oxygen Inactivates Fibrinogen, Factor V, Factor VIII, Factor X, and Platelet Aggregation of Human Blood

Hereditary coproporphyria in Germany: clinical-biochemical studies in 53 patients

New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyria

Compound heterozygous hereditary coproporphyria with fluorescing teeth

Regulation of Pseudomonas aeruginosa hemF and hemN by the dual action of the redox response regulators Anr and Dnr

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