Camille Wicker

Strasbourg, France

Last Updated: 09/26/2026

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Found 14 publications

Amino Acid Deficiency Secondary to Continuous Venovenous Hemofiltration in Acute Decompensation of Organic Acidemias: An Anabolic Dead End?

Amino Acid Deficiency Secondary to Continuous Venovenous Hemofiltration in Acute Decompensation of Organic Acidemias: An Anabolic Dead End?

Journal: Critical care explorations

Published: August 01, 2026

Impact of COVID-19 infection in patients with inherited metabolic diseases: a National Multicenter Study from the French IMDs Healthcare Network for Rare Diseases.

Impact of COVID-19 infection in patients with inherited metabolic diseases: a National Multicenter Study from the French IMDs Healthcare Network for Rare Diseases.

Journal: Orphanet journal of rare diseases

Published: September 19, 2025

Oral D-mannose therapy during pregnancy in a woman with MPI-CDG: A case report and management review.

Oral D-mannose therapy during pregnancy in a woman with MPI-CDG: A case report and management review.

Journal: Molecular genetics and metabolism

Published: September 16, 2025

Standardized emergency protocols to improve the management of patients with suspected or confirmed inherited metabolic disorders (IMDs): An initiative of the French IMDs Healthcare Network for Rare Diseases.

Standardized emergency protocols to improve the management of patients with suspected or confirmed inherited metabolic disorders (IMDs): An initiative of the French IMDs Healthcare Network for Rare Diseases.

Journal: Molecular genetics and metabolism

Published: April 29, 2024

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

Functional analysis of novel variants identified in cis in the PCCB gene in a patient with propionic acidemia.

Functional analysis of novel variants identified in cis in the PCCB gene in a patient with propionic acidemia.

Journal: Gene

Published: August 21, 2023

Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute management.

Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute management.

Journal: Molecular genetics and metabolism

Published: July 27, 2023

French recommendations for the management of glycogen storage disease type III.

French recommendations for the management of glycogen storage disease type III.

Journal: European journal of medical research

Published: August 01, 2022

Sebelipase alfa enzyme replacement therapy in Wolman disease: a nationwide cohort with up to ten years of follow-up.

Sebelipase alfa enzyme replacement therapy in Wolman disease: a nationwide cohort with up to ten years of follow-up.

Journal: Orphanet journal of rare diseases

Published: October 06, 2021

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

Infectious and digestive complications in glycogen storage disease type Ib: Study of a French cohort.

Infectious and digestive complications in glycogen storage disease type Ib: Study of a French cohort.

Journal: Molecular genetics and metabolism reports

Published: March 21, 2020

Administration of gamma-hydroxybutyrate instead of beta-hydroxybutyrate to a liver transplant recipient suffering from propionic acidemia and cardiomyopathy: A case report on a medication prescribing error.

Administration of gamma-hydroxybutyrate instead of beta-hydroxybutyrate to a liver transplant recipient suffering from propionic acidemia and cardiomyopathy: A case report on a medication prescribing error.

Journal: JIMD reports

Published: October 02, 2019

Showing 1-12 of 14

Last Updated: 09/26/2026