Nathalie Bouzamondo
Angers, 49000, France
Last Updated: 09/26/2026
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Found 8 publications
The Severity of Congenital Hypothyroidism With Gland-In-Situ Predicts Molecular Yield by Targeted Next-Generation Sequencing.
Journal: The Journal of clinical endocrinology and metabolism
Published: April 12, 2022
Clinically Symptomatic Resistance to Thyroid Hormone β Syndrome Because of THRB Gene Mosaicism.
Journal: The Journal of clinical endocrinology and metabolism
Published: January 11, 2022
Congenital hypothyroidism and hearing loss without inner ear malformation: Think TPO.
Journal: Clinical genetics
Published: October 08, 2020
Familial Dysalbuminemic Hyperthyroxinemia: An Underdiagnosed Entity.
Journal: Journal of clinical medicine
Published: May 05, 2020
Apparent resistance to thyroid hormones: From biological interference to genetics.
Journal: Annales d'endocrinologie
Published: January 25, 2019
Metabolomics signatures of a subset of RET variants according to their oncogenic risk level.
Journal: Endocrine-related cancer
Published: January 14, 2019
New case of bilateral pheochromocytomas involving the homozygous TMEM127 mutation.
Journal: Clinical genetics
Published: February 06, 2018
Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers.
Journal: Thyroid : official journal of the American Thyroid Association
Published: September 27, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026