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Trends in Molecular Medicine|June 18, 2024
Erythropoietic protoporphyrias: updates and advancesAntoine Poli, Caroline Schmitt, Hervé Puy, et al.
Molecular Autism|April 2, 2020
Loss of the neurodevelopmental disease-associated gene miR-146a impairs neural progenitor differentiation and causes learning and memory deficitsJulien Fregeac, Stéphanie Moriceau, Antoine Poli, et al.
Metabolites|December 23, 2021
Iron, Heme Synthesis and Erythropoietic Porphyrias: A Complex InterplayAntoine Poli, Caroline Schmitt, Boualem Moulouel, et al.
Metabolism: Clinical and Experimental|May 8, 2013
The lactase persistence genotype is associated with body mass index and dairy consumption in the D.E.S.I.R. studyAmel Lamri, Antoine Poli, Nathalie Emery, et al.
Kidney International Reports|July 26, 2021
Renal Function Decline With Small Interfering RNA Silencing Aminolevulinic Acid Synthase 1 (ALAS1)Hélène Lazareth, Antoine Poli, Yohan Bignon, et al.
Clinical Chemistry|August 23, 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 PatientsAntoine Poli, Hana Manceau, Anvi Laetitia Nguyen, et al.
Familial Cancer|September 15, 2016
Hereditary breast and ovarian cancer: successful systematic implementation of a group approach to genetic counsellingPatrick R Benusiglio, Marina Di Maria, Leila Dorling, et al.
Molecular Genetics and Metabolism Reports|March 4, 2021
Identification of novel UROS mutations in a patient with congenital erythropoietic porphyria and efficient treatment by phlebotomyJean-Marc Blouin, Cécile Ged, Ganeko Bernardo-Seisdedos, et al.
American Journal of Medical Genetics. Part A|April 26, 2017
Phosphoglycerate dehydrogenase (PHGDH) deficiency without epilepsy mimicking primary microcephalyAntoine Poli, Yoann Vial, Damien Haye, et al.
La Revue De Medecine Interne|March 19, 2021
[Abnormal urine color assessment: The urine wheel]Edouard Flamarion, Constance Reichert, Caroline Sayegh, et al.
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