Chrystele Bonnemains

Nancy, France

Last Updated: 09/26/2026

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Found 13 publications

Distinct Clinical Courses and Shortened Lifespans in Childhood-Onset DNA Polymerase Gamma Deficiency.

Distinct Clinical Courses and Shortened Lifespans in Childhood-Onset DNA Polymerase Gamma Deficiency.

Journal: Neurology. Genetics

Published: December 04, 2023

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

Health Status of French Young Patients with Inborn Errors of Metabolism with Lifelong Restricted Diet.

Health Status of French Young Patients with Inborn Errors of Metabolism with Lifelong Restricted Diet.

Journal: The Journal of pediatrics

Published: August 23, 2019

Neuropsychological Profile of Children with Early and Continuously Treated Phenylketonuria: Systematic Review and Future Approaches.

Neuropsychological Profile of Children with Early and Continuously Treated Phenylketonuria: Systematic Review and Future Approaches.

Journal: Journal of the International Neuropsychological Society : JINS

Published: April 30, 2019

Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

Journal: Nature communications

Published: February 04, 2018

APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

Journal: Nature communications

Published: May 05, 2017

30 months follow-up of an early enzyme replacement therapy in a severe Morquio A patient: About one case.

30 months follow-up of an early enzyme replacement therapy in a severe Morquio A patient: About one case.

Journal: Molecular genetics and metabolism reports

Published: August 04, 2016

Biotinidase deficiency mimicking neuromyelitis optica beginning at the age of 4: A treatable disease.

Biotinidase deficiency mimicking neuromyelitis optica beginning at the age of 4: A treatable disease.

Journal: Multiple sclerosis (Houndmills, Basingstoke, England)

Published: May 22, 2016

Sandifer's syndrome in a 5-month-old child with suspicion of infantile spasms

Sandifer's syndrome in a 5-month-old child with suspicion of infantile spasms

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: January 19, 2015

Phenylketonuria: new treatments

Phenylketonuria: new treatments

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: March 29, 2013

Prognostic value of early therapeutic alliance in weight recovery: a prospective cohort of 108 adolescents with anorexia nervosa.

Prognostic value of early therapeutic alliance in weight recovery: a prospective cohort of 108 adolescents with anorexia nervosa.

Journal: The Journal of adolescent health : official publication of the Society for Adolescent Medicine

Published: March 13, 2012

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Last Updated: 09/26/2026