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Journal of Human Genetics|October 25, 2019
Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesisArnaud Wiedemann, Céline Chery, David Coelho, et al.
Inflammatory Bowel Diseases|June 12, 2013
Submucosal plexitis as a predictor of postoperative surgical recurrence in Crohn's diseaseAude Bressenot, Jean-Baptiste Chevaux, Nicolas Williet, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2021
Low-frequency Coding Variants Associated With Body Mass Index Affect the Success of Bariatric SurgeryDarlène Antoine, Rosa-Maria Guéant-Rodriguez, Jean-Claude Chèvre, et al.
Clinical Epigenetics|October 5, 2023
A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells development and retinal metabolismKarim Matmat, Jean-Baptiste Conart, Paul-Henri Graindorge, et al.
Cellular and Molecular Gastroenterology and Hepatology|September 3, 2023
MUC13 Cell Surface Mucin Limits Salmonella Typhimurium Infection by Protecting the Mucosal Epithelial BarrierMichael A McGuckin, Julie M Davies, Pascal Felgner, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|April 25, 2024
Multiparametric renal function assessment in cirrhotic patients shows high prevalence of medically actionable changes in multiple modulesRichard Belmonte, Maël Silva-Rodriguez, Françoise Barbé, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 2026
Hyperhomocysteinemia and Vitamin B Deficiency as Potential Aggravating Factors in Huntington's Disease: A Prospective Monocentric StudySalomé Puisieux, Elise Pourié, Céline Bonnet, et al.
European Journal of Clinical Investigation|March 7, 2025
Mid-regional pro-adrenomedullin: A rapid sepsis biomarker for diagnosing spontaneous bacterial peritonitis in cirrhosisAbderrahim Oussalah, Vincent Haghnejad, Maël Silva Rodriguez, et al.
Biochimie|February 14, 2013
Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variantCeline Chery, Alain Hehn, Nadir Mrabet, et al.
Allergy|January 4, 2020
Genetic variants associated with T cell-mediated cutaneous adverse drug reactions: A PRISMA-compliant systematic review-An EAACI position paperAbderrahim Oussalah, Vincent Yip, Cristobalina Mayorga, et al.
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