Late-Onset Erythropoietic Porphyria Caused by a Chromosome 18q Deletion in Erythroid Cells-Reference-Cited by-同舟云学术

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Late-Onset Erythropoietic Porphyria Caused by a Chromosome 18q Deletion in Erythroid Cells

Published:2001-12 Issue:6 Volume:117 Page:1647-1649
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Whatley Sharon D.,Thompson Peter,Hoy Terry,Fisher Paul,Singer Charles,Elder George H.,Aplin Carolyn,Lovell Christopher R.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference23 articles.

1. Molecular analysis of delta-aminolevulinate dehydratase deficiency in a patient with an unusual late-onset porphyria;Akagi;Blood,2000

2. Abnormalities of chromosome 18 in myelodysplastic syndromes and secondary leukemia;Berger;Cancer Genet Cytogenet,1992

3. A molecular defect in human protoporphyria;Brenner;Am J Hum Genet,1992

4. Molecular genetics of congenital erythropoietic porphyria;Desnick;Seminars Liver Dis,1998

5. Erythropoietic protoporphyria presenting in adulthood;Fallon;Arch Dermatol,1989

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1. How I treat erythropoietic protoporphyria and X-linked protoporphyria;Blood;2023-03-10

2. Distribution of protoporphyrin IX in erythrocytes in a case of acquired erythropoietic protoporphyria;Photodiagnosis and Photodynamic Therapy;2021-11

3. Porphyrias: Acute Manifestations;Contemporary Endocrinology;2021

4. Recent advances on porphyria genetics: Inheritance, penetrance & molecular heterogeneity, including new modifying/causative genes;Molecular Genetics and Metabolism;2019-11

5. Erythropoietic Protoporphyria and X-Linked Protoporphyria: pathophysiology, genetics, clinical manifestations, and management;Molecular Genetics and Metabolism;2019-11

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