Author:
Lahiji Arian Pourmehdi,Anderson Karl E.,Chan Amy,Simon Amy,Desnick Robert J.,Ramanujam V.M. Sadagopa
Funder
National Institute of Diabetes and Digestive and Kidney Diseases
National Center for Advancing Translational Sciences
American Porphyria Foundation
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference41 articles.
1. Disorders of heme biosynthesis: X-linked sideroblastic anemia and the porphyrias, the Online Metabolic and Molecular Bases of Inherited Disease;Anderson,2017
2. δ-Aminolevulinate dehydratase (ALAD) porphyria: the first case in North America with two novel ALAD mutations;Akagi;Mol. Genet. Metab.,2006
3. Clinical remission of delta-aminolevulinic acid dehydratase deficiency through suppression of erythroid heme synthesis;Neeleman;Hepatology,2019
4. Acute hepatic porphyrias: current diagnosis & management;Anderson;Mol. Genet. Metab.,2019
5. Excretion of porphyrins in urine and bile after the administration of delta-aminolevulinic acid;Shimizu;J. Lab. Clin. Med.,1978
Cited by
14 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献