Clement Janot

Faculté De Médecine Lyon Est
Lyon, 69008, France

Last Updated: 09/26/2026

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Found 12 publications

A Recurrent Splice Variant Sheds Light on 11β-Hydroxylase Deficiency in a Unique Large Cohort.

A Recurrent Splice Variant Sheds Light on 11β-Hydroxylase Deficiency in a Unique Large Cohort.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 28, 2025

First intragenic inversion of CYP11B1 gene causing 11β-hydroxylase deficiency: a molecular diagnosis easily overlooked.

First intragenic inversion of CYP11B1 gene causing 11β-hydroxylase deficiency: a molecular diagnosis easily overlooked.

Journal: Journal of medical genetics

Published: April 28, 2025

Rare causes of pediatric primary adrenal insufficiency: Data from a large nationwide Tunisian cohort.

Rare causes of pediatric primary adrenal insufficiency: Data from a large nationwide Tunisian cohort.

Journal: Annales d'endocrinologie

Published: April 09, 2025

Orthotopic pituitary tumors generated by stereotaxic GC cell injection in immunocompetent rats.

Orthotopic pituitary tumors generated by stereotaxic GC cell injection in immunocompetent rats.

Journal: Acta neuropathologica communications

Published: March 14, 2025

Meal-induced PYY and GLP1 secretions differently predict long-term weight loss after sleeve gastrectomy.

Meal-induced PYY and GLP1 secretions differently predict long-term weight loss after sleeve gastrectomy.

Journal: Clinical nutrition (Edinburgh, Scotland)

Published: December 15, 2024

Letter to the Editor From Janot et al: « Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia ».

Letter to the Editor From Janot et al: « Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia ».

Journal: The Journal of clinical endocrinology and metabolism

Published: February 01, 2024

Urinary gonadotropin assay on 24-h collections as a tool to detect early central puberty onset in girls: determination of predictive thresholds.

Urinary gonadotropin assay on 24-h collections as a tool to detect early central puberty onset in girls: determination of predictive thresholds.

Journal: Human reproduction (Oxford, England)

Published: November 14, 2023

Neonatal salt wasting syndrome: Aldosterone synthase deficiency caused by a new splicing variant in CYP11B2.

Neonatal salt wasting syndrome: Aldosterone synthase deficiency caused by a new splicing variant in CYP11B2.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: June 07, 2023

Identifying elevated plasma free triiodothyronine levels: age-adapted reference intervals for pediatrics.

Identifying elevated plasma free triiodothyronine levels: age-adapted reference intervals for pediatrics.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: June 28, 2022

MANAGEMENT OF ENDOCRINE DISEASE: Etiology and outcome of acromegaly in patients with a paradoxical GH response to glucose.

MANAGEMENT OF ENDOCRINE DISEASE: Etiology and outcome of acromegaly in patients with a paradoxical GH response to glucose.

Journal: European journal of endocrinology

Published: December 17, 2020

Second edition of the CoBioMe congress

Second edition of the CoBioMe congress

Journal: Annales de biologie clinique

Published: April 19, 2019

First edition of the CoBioMe congress

First edition of the CoBioMe congress

Journal: Annales de biologie clinique

Published: April 07, 2018

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Last Updated: 09/26/2026