Is this you? Create Your Porfile
Avatar

F. Savagner

Network

Latest external collaboration on country level. Dive into details by clicking on the dots.

Explore More

Hotspot

Dive into the research topics where F. Savagner is active.

Explore More

Publication

Featured researches published by F. Savagner.

Clinical Case Reports | 2017

Severe thyrotoxicosis in an infant revealing familial nonautoimmune hyperthyroidism with a novel (C672W) stimulating thyrotropin receptor germline mutation

Isabelle Oliver-Petit; F. Savagner; S. Grunenwald; Magaly Vialon; Thomas Edouard; Philippe Caron

We describe severe thyrotoxicosis in young members of a family with nonautoimmune hyperthyroidism caused by a C672W germline mutation in exon 10 of TSHR gene. In this family, lack of genotype‐phenotype correlation and anticipation across generations could be linked to an increased iodine intake as recently observed in France.

Annales D Endocrinologie | 2018

Hyperthyroïdie gestationnelle familiale (HGF) liée à une nouvelle mutation (Val597Ile) du récepteur de la TSH, hypersensible à l’hormone gonadotrophine chorionique (hGC)

Philippe Caron; S. Broussaud; M. Susini; F. Savagner

20th European Congress of Endocrinology | 2018

Familial gestational hyperthyroidism caused by Val597ile mutant of TSH receptor gene with human chorionic gonadotropin hypersensitivity

Philippe Caron; Marion Susini; F. Savagner

Annales D Endocrinologie | 2017

Une nouvelle mutation hétérozygote du gène du récepteur à la TSH révélée par une hyperthyroïdie sévère du nourrisson

I. Oliver Petit; F. Savagner; S. Grunenwald; Thomas Edouard; Philippe Caron

Archive | 2016

Novel Homozygous Mutation in the Sodium/Iodide Symporter (NIS) Gene Highlight by Next Generation Sequencing (NGS) in a Patient with Congenital Hypothyroidism

Isabelle Oliver Petit; Isabelle Gennero; F. Savagner

Annales D Endocrinologie | 2016

Apport de la technique NGS dans la prise en charge des hypothyroïdies congénitales avec glande en place

F. Savagner; Isabelle Gennero; Thomas Edouard; Audrey Cartault; M. Tauber; I. Oliver-Petit

Annales D Endocrinologie | 2016

Mise en évidence par NGS d’une nouvelle mutation homozygote du gène codant pour NIS chez un patient avec hypothyroïdie congénitale

I. Oliver Petit; Isabelle Gennero; F. Savagner

55th Annual ESPE | 2016

Contribution of Next Generation Sequencing Approach for Management of Congenital Hypothyroidism with Eutopic Thyroid Gland

F. Savagner; Isabelle Gennero; Thomas Edouard; Audrey Cartault; Maithe Tauber; Isabelle Oliver Petit

Annales D Endocrinologie | 2015

Intérêt du dialogue entre endocrinologue et neuropédiatres pour le diagnostic précoce des résistances aux hormones thyroïdiennes par mutation MCT8 : à propos de 2 cas

I. Oliver Petit; C. Cances; C. Hachon Le Camus; F. Savagner

Annales D Endocrinologie | 2015

Le goitre multi nodulaire du sujet jeune est une porte d’entrée diagnostique des mutations de DICER 1

I. Oliver Petit; L. Golmard; A. Buffet; F. Savagner

Explore More

Collaboration

Dive into the F. Savagner's collaboration.

Top Co-Authors
Avatar

Philippe Caron

Paul Sabatier University

View shared research outputs
Top Co-Authors
Avatar

Thomas Edouard

Boston Children's Hospital

View shared research outputs
Top Co-Authors
Avatar

Audrey Cartault

Boston Children's Hospital

View shared research outputs
Top Co-Authors
Avatar

Isabelle Oliver Petit

Paris Diderot University

View shared research outputs
Top Co-Authors
Avatar

L. Golmard

Curie Institute

View shared research outputs
Top Co-Authors
Avatar

Isabelle Oliver-Petit

Boston Children's Hospital

View shared research outputs
Explore More
Researchain Logo
Decentralizing Knowledge