Anne-frederique F. Dessein

Univ. Lille, CNRS, Inserm, UMR9020U1277-CANTHER Cancer Heterogeneity Plasticity And Resistance To Therapies, CHU Lille, 2 Avenue Oscar Lambret
Lille, 59000, France

Last Updated: 09/26/2026

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Found 29 publications

Identification of metabolite biomarkers for pancreatic neuroendocrine tumours using a metabolomic approach.

Identification of metabolite biomarkers for pancreatic neuroendocrine tumours using a metabolomic approach.

Journal: European journal of endocrinology

Published: October 16, 2024

Mitochondrial DNA or Genomic DNA Variant(s): Utility of Exhaustive Sequencing in Leigh Syndrome.

Mitochondrial DNA or Genomic DNA Variant(s): Utility of Exhaustive Sequencing in Leigh Syndrome.

Journal: American journal of medical genetics. Part A

Published: October 03, 2024

Findings from the individualized management of a patient with Acyl-CoA Oxidase-1 (ACOX1) deficiency: A bedside-to-bench-to-bedside strategy.

Findings from the individualized management of a patient with Acyl-CoA Oxidase-1 (ACOX1) deficiency: A bedside-to-bench-to-bedside strategy.

Journal: Molecular genetics and metabolism

Published: June 18, 2024

Metabolism of pancreatic neuroendocrine tumors: what can omics tell us?

Metabolism of pancreatic neuroendocrine tumors: what can omics tell us?

Journal: Frontiers in endocrinology

Published: June 27, 2023

Targeted Metabolomics Analysis Suggests That Tacrolimus Alters Protection against Oxidative Stress.

Targeted Metabolomics Analysis Suggests That Tacrolimus Alters Protection against Oxidative Stress.

Journal: Antioxidants (Basel, Switzerland)

Published: June 23, 2023

Long-term prognosis of fatty-acid oxidation disorders in adults: Optimism despite the limited effective therapies available.

Long-term prognosis of fatty-acid oxidation disorders in adults: Optimism despite the limited effective therapies available.

Journal: European journal of neurology

Published: June 09, 2023

Deafness, Encephalopathy, and Lactic Acidosis: What If It Was an Inborn Metabolic Error?

Deafness, Encephalopathy, and Lactic Acidosis: What If It Was an Inborn Metabolic Error?

Journal: Clinical chemistry

Published: March 03, 2023

Newborn Screening of Primary Carnitine Deficiency: An Overview of Worldwide Practices and Pitfalls to Define an Algorithm before Expansion of Newborn Screening in France.

Newborn Screening of Primary Carnitine Deficiency: An Overview of Worldwide Practices and Pitfalls to Define an Algorithm before Expansion of Newborn Screening in France.

Journal: International journal of neonatal screening

Published: January 01, 2023

Serum Succinate/Fumarate Ratio in Patients With Paraganglioma/Pheochromocytoma Attending an Endocrine Oncogenetic Unit.

Serum Succinate/Fumarate Ratio in Patients With Paraganglioma/Pheochromocytoma Attending an Endocrine Oncogenetic Unit.

Journal: The Journal of clinical endocrinology and metabolism

Published: October 06, 2022

Serum fatty acid profiling in patients with SDHx mutations: New advances on cellular metabolism in SDH deficiency.

Serum fatty acid profiling in patients with SDHx mutations: New advances on cellular metabolism in SDH deficiency.

Journal: Biochimie

Published: May 27, 2022

A novel HADHA variant associated with an atypical moderate and late-onset LCHAD deficiency.

A novel HADHA variant associated with an atypical moderate and late-onset LCHAD deficiency.

Journal: Molecular genetics and metabolism reports

Published: October 05, 2021

Citrin deficiency: Does the reactivation of liver aralar-1 come into play and promote HCC development?

Citrin deficiency: Does the reactivation of liver aralar-1 come into play and promote HCC development?

Journal: Biochimie

Published: May 04, 2021

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Last Updated: 09/26/2026