Arienne Mirmiran
Paris, France
Last Updated: 09/26/2026
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Found 13 publications
Advances in Marfan Syndrome Care: The Limits of Type B Dissection.
Journal: The Annals of thoracic surgery
Published: September 05, 2025
A large French family with TGFBR2 pathogenic variant: illustration of variability.
Journal: Orphanet journal of rare diseases
Published: April 04, 2025
Management of erythropoietic protoporphyria with cholestatic liver disease: A case report.
Journal: Molecular genetics and metabolism reports
Published: August 17, 2023
Givosiran in acute intermittent porphyria: A personalized medicine approach.
Journal: Molecular genetics and metabolism
Published: October 30, 2021
Iron, Heme Synthesis and Erythropoietic Porphyrias: A Complex Interplay.
Journal: Metabolites
Published: October 29, 2021
Renal Function Decline With Small Interfering RNA Silencing Aminolevulinic Acid Synthase 1 (ALAS1).
Journal: Kidney international reports
Published: March 01, 2021
TSPO2 translocates 5-aminolevulinic acid into human erythroleukemia cells.
Journal: Biology of the cell
Published: November 19, 2019
Phlebotomy as an efficient long-term treatment of congenital erythropoietic porphyria.
Journal: Haematologica
Published: July 11, 2019
Regulation and tissue-specific expression of δ-aminolevulinic acid synthases in non-syndromic sideroblastic anemias and porphyrias.
Journal: Molecular genetics and metabolism
Published: October 17, 2018
Erythroid-Progenitor-Targeted Gene Therapy Using Bifunctional TFR1 Ligand-Peptides in Human Erythropoietic Protoporphyria.
Journal: American journal of human genetics
Published: June 24, 2018
Recurrent attacks of acute hepatic porphyria: major role of the chronic inflammatory response in the liver.
Journal: Journal of internal medicine
Published: March 03, 2018
From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyria.
Journal: Human molecular genetics
Published: October 13, 2017
Last Updated: 09/26/2026