Delphine Lamireau

Bordeaux, France

Last Updated: 09/26/2026

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Found 25 publications

Elamipretide in pediatric Barth syndrome: from heart failure to school return.

Elamipretide in pediatric Barth syndrome: from heart failure to school return.

Journal: Orphanet journal of rare diseases

Published: October 03, 2025

Immunization coverage and timeliness of vaccination in young patients with inborn errors of metabolism: a French multicentric study.

Immunization coverage and timeliness of vaccination in young patients with inborn errors of metabolism: a French multicentric study.

Journal: Orphanet journal of rare diseases

Published: December 11, 2024

Case report: Unveiling genetic and phenotypic variability in Nonketotic hyperglycinemia: an atypical early onset case associated with a novel GLRX5 variant.

Case report: Unveiling genetic and phenotypic variability in Nonketotic hyperglycinemia: an atypical early onset case associated with a novel GLRX5 variant.

Journal: Frontiers in genetics

Published: May 13, 2024

New alternatives to holder pasteurization in processing donor milk in human milk banks.

New alternatives to holder pasteurization in processing donor milk in human milk banks.

Journal: Frontiers in nutrition

Published: March 29, 2024

Real-World Experience of Carglumic Acid for Methylmalonic and Propionic Acidurias: An Interim Analysis of the Multicentre Observational PROTECT Study.

Real-World Experience of Carglumic Acid for Methylmalonic and Propionic Acidurias: An Interim Analysis of the Multicentre Observational PROTECT Study.

Journal: Drugs in R&D

Published: October 30, 2023

Case report: Two siblings with very late onset of holocarboxylase synthase deficiency and a mini-review.

Case report: Two siblings with very late onset of holocarboxylase synthase deficiency and a mini-review.

Journal: Frontiers in genetics

Published: June 28, 2023

Systemic primary carnitine deficiency induces severe arrhythmia due to shortening of QT interval.

Systemic primary carnitine deficiency induces severe arrhythmia due to shortening of QT interval.

Journal: Molecular genetics and metabolism

Published: June 05, 2023

Systemic corticosteroids for the treatment of acute episodes of rhabdomyolysis in lipin-1-deficient patients.

Systemic corticosteroids for the treatment of acute episodes of rhabdomyolysis in lipin-1-deficient patients.

Journal: Journal of inherited metabolic disease

Published: August 30, 2022

Individual and Family Determinants for Quality of Life in Parents of Children with Inborn Errors of Metabolism Requiring a Restricted Diet: A Multilevel Analysis Approach.

Individual and Family Determinants for Quality of Life in Parents of Children with Inborn Errors of Metabolism Requiring a Restricted Diet: A Multilevel Analysis Approach.

Journal: The Journal of pediatrics

Published: February 07, 2022

Determinants of Quality of Life in Children with Inborn Errors of Metabolism Receiving a Restricted Diet.

Determinants of Quality of Life in Children with Inborn Errors of Metabolism Receiving a Restricted Diet.

Journal: The Journal of pediatrics

Published: May 12, 2021

It's time to change the recommendations on COVID-19 and human milk donations.

It's time to change the recommendations on COVID-19 and human milk donations.

Journal: Acta paediatrica (Oslo, Norway : 1992)

Published: December 08, 2020

Real-world management of maple syrup urine disease (MSUD) metabolic decompensations with branched chain amino acid-free formulas in France and Germany: A retrospective observational study.

Real-world management of maple syrup urine disease (MSUD) metabolic decompensations with branched chain amino acid-free formulas in France and Germany: A retrospective observational study.

Journal: JIMD reports

Published: October 17, 2020

Showing 1-12 of 25

Last Updated: 09/26/2026