Erythropoietic protoporphyria: Altered phenotype after bone marrow transplantation for myelogenous leukemia in a patient heteroallelic for ferrochelatase gene mutations
- 1 June 2002
- journal article
- case report
- Published by Elsevier in Journal of the American Academy of Dermatology
- Vol. 46 (6) , 861-866
- https://doi.org/10.1067/mjd.2002.120460
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- New insights into the pathogenesis of erythropoietic protoporphyria and their impact on patient care.European Journal of Pediatrics, 2000
- Haplotype Analysis of Families with Erythropoietic Protoporphyria and Novel Mutations of the Ferrochelatase GeneJournal of Investigative Dermatology, 1999
- Systematic Analysis of Molecular Defects in the Ferrochelatase Gene from Patients with Erythropoietic ProtoporphyriaAmerican Journal of Human Genetics, 1998
- Erythropoietic protoporphyriaJournal of Inherited Metabolic Disease, 1997
- Erythropoietic protoporphyriaBritish Journal of Dermatology, 1994
- Recessive inheritance of erythropoietic protoporphyria with liver failureThe Lancet, 1994
- Cyclosporine, Methotrexate, and Prednisone Compared with Cyclosporine and Prednisone for Prophylaxis of Acute Graft-versus-Host DiseaseNew England Journal of Medicine, 1993
- Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase geneBiochemical and Biophysical Research Communications, 1991
- Genetic aspects of erythropoietic protoporphyriaAnnals of Human Genetics, 1984
- Rates of Plasma Porphrin Disappearance in Fluorescent Vs. Red Incandescent Light ExposureJournal of Investigative Dermatology, 1977