Claire Gay

Lyon, France

Last Updated: 09/26/2026

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Found 12 publications

Efficacy and Safety of Second-Line Advanced Therapy After Vedolizumab in Ulcerative Colitis: A Multicenter Cohort Study From the GETAID.

Efficacy and Safety of Second-Line Advanced Therapy After Vedolizumab in Ulcerative Colitis: A Multicenter Cohort Study From the GETAID.

Journal: United European gastroenterology journal

Published: October 19, 2025

Efficacy and Safety of Second-Line Advanced Therapy After Vedolizumab in Ulcerative Colitis: A Multicenter Cohort Study From the GETAID.

Efficacy and Safety of Second-Line Advanced Therapy After Vedolizumab in Ulcerative Colitis: A Multicenter Cohort Study From the GETAID.

Journal: United European gastroenterology journal

Published: October 19, 2025

Neurological and psychiatric issues in 187 adults with early-treated PKU: The ECOPHEN study.

Neurological and psychiatric issues in 187 adults with early-treated PKU: The ECOPHEN study.

Journal: Molecular genetics and metabolism

Published: September 18, 2025

Neuropsychological profile of French adults with early-treated phenylketonuria: a multicenter study.

Neuropsychological profile of French adults with early-treated phenylketonuria: a multicenter study.

Journal: Journal of neurology

Published: September 18, 2024

Bone mineral density in French adults with early-treated phenylketonuria.

Bone mineral density in French adults with early-treated phenylketonuria.

Journal: Molecular genetics and metabolism

Published: August 21, 2024

Fructose-1,6-bisphosphatase deficiency causes fatty liver disease and requires long-term hepatic follow-up.

Fructose-1,6-bisphosphatase deficiency causes fatty liver disease and requires long-term hepatic follow-up.

Journal: Journal of inherited metabolic disease

Published: August 25, 2021

Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic study.

Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic study.

Journal: EBioMedicine

Published: November 30, 2019

Betaine anhydrous in homocystinuria: results from the RoCH registry.

Betaine anhydrous in homocystinuria: results from the RoCH registry.

Journal: Orphanet journal of rare diseases

Published: November 07, 2018

A pernicious cause of infant hypotonia

A pernicious cause of infant hypotonia

Journal: Presse medicale (Paris, France : 1983)

Published: October 18, 2017

Neurocognitive profiles in MSUD school-age patients.

Neurocognitive profiles in MSUD school-age patients.

Journal: Journal of inherited metabolic disease

Published: October 09, 2016

Genotype-phenotype associations in French patients with phenylketonuria and importance of genotype for full assessment of tetrahydrobiopterin responsiveness.

Genotype-phenotype associations in French patients with phenylketonuria and importance of genotype for full assessment of tetrahydrobiopterin responsiveness.

Journal: Orphanet journal of rare diseases

Published: August 07, 2015

Inaugural cerebral sinovenous thrombosis revealing homocystinuria in a 2-year-old boy.

Inaugural cerebral sinovenous thrombosis revealing homocystinuria in a 2-year-old boy.

Journal: Journal of child neurology

Published: March 07, 2014

Showing 1-12 of 12

Last Updated: 09/26/2026