How RNF216 Variants Link Dementia, Hypogonadism and Severe Ataxia – SEF
French Society of Endocrinology (SEF) shared a post on LinkedIn about a paper by Jacques Young et al. published in The Journal of Clinical Endocrinology and Metabolism:
“Research Newsletter n°44 – Focus on …
‘RNF216 variants found in patients with dementia, hypogonadotropic hypogonadism, and severe ataxia deregulate autophagy’ (J. Young; I. Beau)
Did you know that since 2011 the SFE has been publishing a newsletter research carefully prepared by Prof. Hubert Vaudry?
This newsletter highlights some articles published by French-speaking teams in the major journals of the discipline and has a double objective:
- Demonstrate the vitality of basic and/or translational research in the laboratories of the Francophone community
- Strengthen the links between the SFE and fundamental endocrinologists
For this month of April, the SFE has decided to highlight the work of Prof. Jacques Young and Dr. Isabelle Beau for their article published in The Journal of Clinical Endocrinology and Metabolism, (Volume 111, Issue 5, May 2026, Pages 1278–1286) and which is part of the SFE rare disease research grant obtained in 2021.
Link to publication.
i️ All research newsletters are available in the SFE media library.
Happy reading!”
Title: RNF216 Variants Found in Patients With Dementia, Hypogonadotropic Hypogonadism, and Severe Ataxia Deregulate Autophagy
Authors: Jacques Young, Inès Abdennebi, Marion Le Saëc, Françoise Magnin, Larbi Amazit, Peter Kamenický, Luigi Maione, Jérôme Bouligand, Isabelle Beau
Proceed to the pages attached to the post.
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