Clinical Remission of Delta‐Aminolevulinic Acid Dehydratase Deficiency Through Suppression of Erythroid Heme Synthesis-Reference-Cited by-同舟云学术

Clinical Remission of Delta‐Aminolevulinic Acid Dehydratase Deficiency Through Suppression of Erythroid Heme Synthesis

Published:2019-06-06 Issue:1 Volume:70 Page:434-436
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Neeleman Rochus A.¹^ORCID,van Beers Eduard J.²,Friesema Edith C.¹,Koole‐Lesuis Rita¹,van der Pol Willem L.³,Wilson J.H. Paul¹,Langendonk Janneke G.¹

Affiliation:

1. Porphyria Center Rotterdam, Center for Lysosomal and Metabolic Disease, Department of Internal Medicine, Erasmus MC University Medical Center Rotterdam Rotterdam the Netherlands

2. Van Creveldkliniek University Medical Center Utrecht Utrecht the Netherlands

3. Department of Neurology and Neurosurgery Brain Center Rudolf Magnus, University Medical Center Utrecht Utrecht the Netherlands

Publisher

Wiley

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hep.30543

Reference4 articles.

1. ALAD Porphyria

2. Liver transplantation in a boy with acute porphyria due to aminolaevulinate dehydratase deficiency;Thunell S;Eur J Clin Chem Clin Biochem,1992

3. Hereditary hepatic porphyria due to homozygous δ-aminolevulinic acid dehydratase deficiency: studies in lymphocytes and erythrocytes

4. GouE ChanA PenzC QuerbesW SimonA AndersonKE.5‐Aminolevulinate dehydratase porphyria (ADP): evidence for hepatic ALAS1 induction. Poster and Oral Presentation International Congress on Porphyrins and Porphyrias; June 27 2017; Palais de la Bourse Bordeaux France.

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