INHERITANCE IN PROTOPORPHYRIA COMPARISON OF HÆM SYNTHETASE ACTIVITY IN SKIN FIBROBLASTS WITH CLINICAL FEATURES

This publication has 18 references indexed in Scilit:

• Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts.
  Journal of Clinical Investigation, 1975
• Hepatic disease in erythropoietic protoporphyria
  The American Journal of Medicine, 1975
• Decreased Haem Synthetase Activity in Blood Cells of Patients with Erythropoietic Protoporphyria
  European Journal of Clinical Investigation, 1975
• Correlation of C-Type Virus (WF-1) Production and Heme Synthesis in a Rat Fibroblastic Cell Line
  Experimental Biology and Medicine, 1974
• Biochemical Defects in Two Types of Human Hepatic Porphyria
  New England Journal of Medicine, 1970
• Fluorescing erythrocytes and porphyrin screening tests on urine, stool, and blood. Investigation of photosensitivity
  Archives of Dermatology, 1967
• HISTOCHEMISTRY OF THE SKIN IN ERYTHROPOIETIC PROTOPORPHYRIA*
  British Journal of Dermatology, 1966
• Erythropoietic protoporphyria: A new type of inborn error of metabolism
  The American Journal of Medicine, 1963
• Metal specificity of the iron-protoporphyrin chelating enzyme from rat liver
  Biochimica et Biophysica Acta, 1961
• ERYTHROPOIETIC PROTOPORPHYRIA A NEW PORPHYRIA SYNDROME WITH SOLAR URTICARIA DUE TO PROTOPORPHYRINqMIA
  The Lancet, 1961