All Research Papers Published In annales d'endocrinologie

Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.

Genetic mechanisms of primary aldosteronism.

Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohort.

Genome architecture in endocrine diseases: X-Linked Acrogigantism (X-LAG) syndrome.

Y chromosome and male fertility: The AZF genes and their deletion.

NGS versus exome versus genome wide: Advantages? Disadvantages?

Prenatal Exposure to Parabens: Associations with Reproductive Hormone Alterations Prenatal Paraben Exposure and Reproductive Hormones.

Appropriate thyroid test ordering: when clinical excellence meets environmental sustainability.

Mechanisms controlling genomic imprinting and their dysregulation in human imprinting disorders.

THE KEY DATA FROM THE 2025 ESE/ESPE CONGRESS: News on impaired sensitivity to thyroid hormone syndromes.