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

Por Oliver‐Petit, Isabelle, Savagner, Frédérique, Grunenwald, Solange, Vialon, Magaly, Edouard, Thomas, Caron, Philippe
Publicado no Clin Case Rep (2017)

Local recurrence of pheochromocytoma in multiple endocrine neoplasia type 2A: a diagnostic and therapeutic challenge

Por Tramunt, Blandine, Buffet, Alexandre, Grunenwald, Solange, Vezzosi, Delphine, Bennet, Antoine, Huyghe, Eric, Zerdoud, Slimane, Caron, Philippe
Publicado no Clin Case Rep (2016)

A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL

Por Bourdeau, Isabelle, Grunenwald, Solange, Burnichon, Nelly, Khalifa, Emmanuel, Dumas, Nadine, Binet, Marie-Claire, Nolet, Serge, Gimenez-Roqueplo, Anne-Paule
Publicado no J Clin Endocrinol Metab (2016)

First case report of an adrenocortical carcinoma caused by a BRCA2 mutation

Por El Ghorayeb, Nada, Grunenwald, Solange, Nolet, Serge, Primeau, Vanessa, Côté, Stéphanie, Maugard, Christine M., Lacroix, André, Gaboury, Louis, Bourdeau, Isabelle
Publicado no Medicine (Baltimore) (2016)