Murielle Assoun

Paris, France

Last Updated: 09/26/2026

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Found 13 publications

Nutritional Management in Severe Methylmalonic and Propionic Acidemias: How Much Medical Food Is Too Much?

Nutritional Management in Severe Methylmalonic and Propionic Acidemias: How Much Medical Food Is Too Much?

Journal: Journal of inherited metabolic disease

Published: August 01, 2025

Pubertal origin of growth retardation in inborn errors of protein metabolism: A longitudinal cohort study.

Pubertal origin of growth retardation in inborn errors of protein metabolism: A longitudinal cohort study.

Journal: Molecular genetics and metabolism

Published: September 25, 2023

Enteral tube feeding in patients receiving dietary treatment for metabolic diseases: A retrospective analysis in a large French cohort.

Enteral tube feeding in patients receiving dietary treatment for metabolic diseases: A retrospective analysis in a large French cohort.

Journal: Molecular genetics and metabolism reports

Published: September 22, 2020

Dietary practices in methylmalonic acidaemia: a European survey.

Dietary practices in methylmalonic acidaemia: a European survey.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: June 19, 2019

Weaning practices in phenylketonuria vary between health professionals in Europe.

Weaning practices in phenylketonuria vary between health professionals in Europe.

Journal: Molecular genetics and metabolism reports

Published: October 12, 2018

Early feeding practices in infants with phenylketonuria across Europe.

Early feeding practices in infants with phenylketonuria across Europe.

Journal: Molecular genetics and metabolism reports

Published: June 07, 2018

Dietary practices in propionic acidemia: A European survey.

Dietary practices in propionic acidemia: A European survey.

Journal: Molecular genetics and metabolism reports

Published: July 05, 2017

Long-term metabolic follow-up and clinical outcome of 35 patients with maple syrup urine disease.

Long-term metabolic follow-up and clinical outcome of 35 patients with maple syrup urine disease.

Journal: Journal of inherited metabolic disease

Published: April 04, 2017

Dietary practices in isovaleric acidemia: A European survey.

Dietary practices in isovaleric acidemia: A European survey.

Journal: Molecular genetics and metabolism reports

Published: January 28, 2017

Update on Lysinuric Protein Intolerance, a Multi-faceted Disease Retrospective cohort analysis from birth to adulthood.

Update on Lysinuric Protein Intolerance, a Multi-faceted Disease Retrospective cohort analysis from birth to adulthood.

Journal: Orphanet journal of rare diseases

Published: July 22, 2016

Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach.

Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach.

Journal: Molecular genetics and metabolism

Published: February 12, 2015

Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia.

Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia.

Journal: Orphanet journal of rare diseases

Published: March 07, 2014

Showing 1-12 of 13

Last Updated: 09/26/2026