Results 121 to 130 of about 601 (148)
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Blood
Introduction PORT-77 is an orally bioavailable inhibitor of the ABCG2 (also known as BCRP) transport protein and is under development for the treatment of EPP. EPP is a rare, genetic form of photodermatosis resulting from autosomal recessive mutations in ferrochelatase (FECH ...
Bhavik Shah +10 more
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Introduction PORT-77 is an orally bioavailable inhibitor of the ABCG2 (also known as BCRP) transport protein and is under development for the treatment of EPP. EPP is a rare, genetic form of photodermatosis resulting from autosomal recessive mutations in ferrochelatase (FECH ...
Bhavik Shah +10 more
openaire +1 more source
Zeitschrift fur Hautkrankheiten, 1981
The case of a 29 year old man is presented, who showed 'sunburn like' reactions following short exposures to light since early childhood. Demonstration of fluorocytes and analysis of porphyrins confirmed the diagnosis of erythropoietic protoporphyria (EPP).
W, Meigel, G, Schaeg, G, Goerz
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The case of a 29 year old man is presented, who showed 'sunburn like' reactions following short exposures to light since early childhood. Demonstration of fluorocytes and analysis of porphyrins confirmed the diagnosis of erythropoietic protoporphyria (EPP).
W, Meigel, G, Schaeg, G, Goerz
openaire +1 more source
Afamelanotide for prevention of phototoxicity in erythropoietic protoporphyria
Expert Review of Clinical Pharmacology, 2021Janneke Langendonk +2 more
exaly
Evidence in the UK Biobank for the underdiagnosis of erythropoietic protoporphyria
Genetics in Medicine, 2021Zhaozhong Zhu +2 more
exaly
Genetic Analysis of Erythropoietic Protoporphyria (EPP) the Erythrocyte Fluorescence Method
1968K. D. Wuepper, J. H. Epstein
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Remission of erythropoietic protoporphyria (EPP) during pregnancy – Experience of two patients
JDDG: Journal der Deutschen Dermatologischen GesellschaftGressenberger Paul, Hofer Angelika
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