Sophie Cholet
Paris, France
Last Updated: 09/26/2026
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Found 24 publications
N-Glycan-Dependent Proinflammatory Effects of IgM in Anti-MAG Neuropathy.
Journal: Neurology(R) neuroimmunology & neuroinflammation
Published: July 31, 2025
The Diversity of Oligosaccharide Composition in Rabbit Milk and Its Association with the Development of the Cecal Microbiota and the Survival of Young Rabbits.
Journal: The Journal of nutrition
Published: May 20, 2025
ATP6AP2-Related Disease Caused by Splicing Defects: Abnormal Glycosylation and the First Affected Female.
Journal: Journal of inherited metabolic disease
Published: April 08, 2025
Efficacy of oral manganese and D-galactose therapy in a patient bearing a novel TMEM165 variant.
Journal: Translational research : the journal of laboratory and clinical medicine
Published: July 17, 2023
"Hide and seek": Misleading transferrin variants in PMM2-CDG complicate diagnostics.
Journal: Proteomics. Clinical applications
Published: April 14, 2023
MAGT1 deficiency in XMEN disease is associated with severe platelet dysfunction and impaired platelet glycoprotein N-glycosylation.
Journal: Journal of thrombosis and haemostasis : JTH
Published: January 11, 2023
SLC37A4-CDG: New biochemical insights for an emerging congenital disorder of glycosylation with major coagulopathy.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: June 08, 2021
Normal transferrin patterns in congenital disorders of glycosylation with Golgi homeostasis disruption: apolipoprotein C-III at the rescue!
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: May 18, 2021
MAN1B1-CDG: Three new individuals and associated biochemical profiles.
Journal: Molecular genetics and metabolism reports
Published: May 06, 2021
Trapped ion mobility spectrometry time-of-flight mass spectrometry for high throughput and high resolution characterization of human milk oligosaccharide isomers.
Journal: Analytica chimica acta
Published: May 04, 2021
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.
Journal: American journal of human genetics
Published: February 04, 2021
Evaluation of erythropoietin biosimilars Epotin™, Hemax® and Jimaixin™ by electrophoretic methods used for doping control analysis and specific N-glycan analysis revealed structural differences from original epoetin alfa drug Eprex®.
Journal: Journal of pharmaceutical and biomedical analysis
Published: October 02, 2020
Last Updated: 09/26/2026