Antoine Poli
Gif-sur-yvette, France
Last Updated: 09/26/2026
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Found 18 publications
Nontargeted urine metabolomic analysis of acute intermittent porphyria reveals novel interactions between bile acids and heme metabolism: New promising biomarkers for the long-term management of patients.
Journal: Journal of inherited metabolic disease
Published: June 06, 2024
Erythropoietic protoporphyrias: updates and advances.
Journal: Trends in molecular medicine
Published: February 28, 2024
Severe Perinatal Presentations of Günther's Disease: Series of 20 Cases and Perspectives.
Journal: Life (Basel, Switzerland)
Published: November 25, 2023
Successful treatment of congenital erythropoietic porphyria using matched unrelated hematopoietic stem cell transplantation in an adult: A case report.
Journal: Skin health and disease
Published: November 16, 2023
The role of allogeneic stem cell transplantation in severe erythropoietic protoporphyria in adults and young adults: timing and modalities.
Journal: Hematology, transfusion and cell therapy
Published: August 22, 2023
Management of erythropoietic protoporphyria with cholestatic liver disease: A case report.
Journal: Molecular genetics and metabolism reports
Published: August 17, 2023
Quantification of Urine and Plasma Porphyrin Precursors Using LC-MS in Acute Hepatic Porphyrias: Improvement in Routine Diagnosis and in the Monitoring of Kidney Failure Patients.
Journal: Clinical chemistry
Published: March 08, 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
Abnormal urine color assessment: The urine wheel
Journal: La Revue de medecine interne
Published: January 30, 2021
Identification of novel UROS mutations in a patient with congenital erythropoietic porphyria and efficient treatment by phlebotomy.
Journal: Molecular genetics and metabolism reports
Published: December 01, 2020
Last Updated: 09/26/2026