Publications by authors named "Anne-Frederique Dessein"

26Publications

[Recommendations for urinary organic acids analysis].

Ann Biol Clin (Paris) 2020 10;78(5):547-554

Laboratoire des maladies héréditaires du métabolisme, Service de biochimie, biologie moléculaire et toxicologie environnementale, CHU Grenoble-Alpes, Grenoble, France.

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October 2020

[Recommendations for acylcarnitine profile analysis].

Ann Biol Clin (Paris) 2020 10;78(5):537-546

Centre de biologie pathologie génétique, UF métabolisme général et maladies rares, CHU Lille, France.

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October 2020

[Pregnancy in metabolic diseases with hepatic expression: what risks for the mother and the child?]

Ann Biol Clin (Paris) 2019 12;77(6):605-618

CHU Lille, Service de biochimie "Hormonologie, métabolisme-nutrition, oncologie", Université de Lille, Lille, France.

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December 2019

Child with Discrepant Urine Protein Results.

Clin Chem 2019 11;65(11):1465-1466

Institute of Biochemistry, Biology and Pathology Center, Lille University Hospital.

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November 2019

Abnormal Ketone Bodies in a 22-Month-Old Boy Presenting with Recurrent Vomiting and Metabolic Acidosis.

Clin Chem 2019 11;65(11):1460-1462

CHU Lille, Centre de Biologie Pathologie Génétique, UF Métabolisme Général et Maladies Rares, F-59000 Lille, France;

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November 2019

First-line Screening of OXPHOS Deficiencies Using Microscale Oxygraphy in Human Skin Fibroblasts: A Preliminary Study.

Int J Med Sci 2019 7;16(7):931-938. Epub 2019 Jun 7.

Univ. Lille, Inserm, UMR-S 1172 - JPArc - Centre de Recherche Jean-Pierre AUBERT Neurosciences et Cancer, F-59000 Lille, France.

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February 2020

Fluxomic assay-assisted diagnosis orientation in a cohort of 11 patients with myopathic form of CPT2 deficiency.

Mol Genet Metab 2018 04 12;123(4):441-448. Epub 2018 Feb 12.

Department of Biochemistry and Molecular Biology, Laboratory of Endocrinology, Metabolism-Nutrition, Oncology, Biology Pathology Center, CHRU Lille, 59037 Lille, France; Univ. Lille, RADEME - Maladies RAres du Développement et du Métabolisme: du phénotype au génotype et à la Fonction, Lille, EA 7364, France; Inserm, Lille, France. Electronic address:

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April 2018

Fluxomic evidence for impaired contribution of short-chain acyl-CoA dehydrogenase to mitochondrial palmitate β-oxidation in symptomatic patients with ACADS gene susceptibility variants.

Clin Chim Acta 2017 Aug 19;471:101-106. Epub 2017 May 19.

Department of Biochemistry and Molecular Biology, Laboratory of Hormonology, Metabolism-Nutrition & Oncology (HMNO), Center of Biology and Pathology (CBP) Pierre-Marie Degand, CHRU Lille, France; Univ. Lille, EA 7364 - RADEME - Maladies RAres du Développement et du Métabolisme: du phénotype au génotype et à la Fonction, Lille, France; Inserm, Lille, France. Electronic address:

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August 2017

A fast method for high resolution oxymetry study of skeletal muscle mitochondrial respiratory chain complexes.

Anal Biochem 2017 07 26;528:57-62. Epub 2017 Apr 26.

Department of Biochemistry and Molecular Biology, Laboratory of Hormonology, Metabolism-Nutrition & Oncology (HMNO), Center of Biology and Pathology (CBP) Pierre-Marie Degand, CHRU Lille, France; Univ. Lille, EA 7364 - RADEME - Maladies RAres du Développement et du Métabolisme: du phénotype au génotype et à la Fonction, Lille, France; Inserm, Lille, France. Electronic address:

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July 2017

Creatine biosynthesis and transport in health and disease.

Biochimie 2015 Dec 2;119:146-65. Epub 2015 Nov 2.

Biochemistry and Molecular Biology, Hormonology-Metabolism-Nutrition & Oncology (HMNO), Center of Biology & Pathology (CBP) Pierre-Marie Degand, CHRU Lille, 59037 Lille, France; RADEME Research Team for Rare Metabolic and Developmental Diseases, EA 7364, Université Lille 2, Lille, France; Inserm, Lille, France. Electronic address:

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December 2015

Colon cancer cells escape 5FU chemotherapy-induced cell death by entering stemness and quiescence associated with the c-Yes/YAP axis.

Clin Cancer Res 2014 Feb 9;20(4):837-46. Epub 2013 Dec 9.

Authors' Affiliations: INSERM U837 Team 4 "Molecular and Cellular Targeting of Cancers"; SIRIC ONCOLille; INSERM U837 Team 5 "Mucins, Epithelial Differentiation, and Carcinogenesis" Jean-Pierre Aubert Research Centre, Université Lille and CHU, Univ Nord de France; Unit of Biostatistics; Department of Digestive Surgery and Transplantation; Department of Medical Oncology, CHU, Univ Nord de France; IBL UMR-8161 CNRS, Université Lille Nord de France, Institut Pasteur, Lille; IRI USR 3078 CNRS, Villeneuve d'Ascq; INSERM U938, Molecular and Clinical Oncology, Hôpital Saint Antoine, Université Pierre et Marie Curie 6, Paris, France; and The University of Texas MD Anderson Cancer Center, Houston, Texas.

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February 2014

A Novel Mutation in CPT1A Resulting in Hepatic CPT Deficiency.

JIMD Rep 2012 31;6:7-14. Epub 2012 Jan 31.

Laboratory of Hormonology, Metabolism-Nutrition & Oncology (HMNO), Center of Biology and Pathology, CHRU Lille, 59037, Lille, France.

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February 2013