Photosensitivity papules--a cutaneous sign of systemic disease: erythropoietic protoporphyria.

Erythropoietic protoporphyria.

Erythropoietic protoporphyria.

Erythropoietic protoporphyria, transfusion therapy and liver disease.

Mechanisms of photosensitivity in porphyric patients with special emphasis on erythropoietic protoporphyria.

Erythropoietic protoporphyria. Hepatic implications.

Erythropoietic protoporphyria with onycholysis.

Erythropoietic protoporphyria and hepatic complications.

A case of erythropoietic protoporphyria.

Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease.

Erythropoietic protoporphyria. 10 years experience.

Liver inclusions in erythropoietic protoporphyria.

Erythropoietic protoporphyria and lead intoxication: the molecular basis for difference in cutaneous photosensitivity. II. Different binding of erythrocyte protoporphyrin to hemoglobin.

A national register for erythropoietic protoporphyria.

Afamelanotide (CUV1647) in dermal phototoxicity of erythropoietic protoporphyria.

Laparoscopic cholecystectomy in a patient with erythropoietic protoporphyria.

[Erythropoietic protoporphyria: porphyrin content of a gall-stone (author's transl)].

Mouse model for protoporphyria. III. Experimental production of chronic erythropoietic protoporphyria-like skin lesions.

Role of ABCG2 in liver injury associated with erythropoietic protoporphyria.

Orthodontic treatment considerations for a patient with erythropoietic protoporphyria.

Human erythropoietic protoporphyria: two point mutations in the ferrochelatase gene.

Narrowband ultraviolet B phototherapy in erythropoietic protoporphyria: case series.

Blastic plasmacytoid dendritic cell neoplasm following acquired erythropoietic protoporphyria.

Erythropoietic protoporphyria and lead intoxication: the molecular basis for difference in cutaneous photosensitivity. I. Different rates of disappearance of protoporphyrin from the erythrocytes, both in vivo and in vitro.

Education and Imaging: hepatology: portal vein cavernoma imitating cholangiocarcinoma in a patient with erythropoietic protoporphyria.

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Erythropoietic protoporphyria.

Erythropoietic protoporphyria.

Erythropoietic protoporphyria, transfusion therapy and liver disease.

Mechanisms of photosensitivity in porphyric patients with special emphasis on erythropoietic protoporphyria.

Erythropoietic protoporphyria. Hepatic implications.

Erythropoietic protoporphyria with onycholysis.

Erythropoietic protoporphyria and hepatic complications.

A case of erythropoietic protoporphyria.

Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease.

Erythropoietic protoporphyria. 10 years experience.

Liver inclusions in erythropoietic protoporphyria.

Erythropoietic protoporphyria and lead intoxication: the molecular basis for difference in cutaneous photosensitivity. II. Different binding of erythrocyte protoporphyrin to hemoglobin.

A national register for erythropoietic protoporphyria.

Afamelanotide (CUV1647) in dermal phototoxicity of erythropoietic protoporphyria.

Laparoscopic cholecystectomy in a patient with erythropoietic protoporphyria.

[Erythropoietic protoporphyria: porphyrin content of a gall-stone (author's transl)].

Mouse model for protoporphyria. III. Experimental production of chronic erythropoietic protoporphyria-like skin lesions.

Role of ABCG2 in liver injury associated with erythropoietic protoporphyria.

Orthodontic treatment considerations for a patient with erythropoietic protoporphyria.

Human erythropoietic protoporphyria: two point mutations in the ferrochelatase gene.

Narrowband ultraviolet B phototherapy in erythropoietic protoporphyria: case series.

Blastic plasmacytoid dendritic cell neoplasm following acquired erythropoietic protoporphyria.

Erythropoietic protoporphyria and lead intoxication: the molecular basis for difference in cutaneous photosensitivity. I. Different rates of disappearance of protoporphyrin from the erythrocytes, both in vivo and in vitro.

Education and Imaging: hepatology: portal vein cavernoma imitating cholangiocarcinoma in a patient with erythropoietic protoporphyria.

Photosensitivity papules--a cutaneous sign of systemic disease: erythropoietic protoporphyria.

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