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Cancers|October 14, 2023
Molecular Basis and Natural History of Medullary Thyroid Cancer: It is (Almost) All in the RETNicolas Sahakian, Frédéric Castinetti, Pauline RomanetAnnales D'Endocrinologie|March 22, 2026
How has genetics changed the diagnosis and care of multiple endocrine neoplasia type 2? The merits and pitfalls of a genetic-based diagnostic and therapeutic approachFrederic Castinetti, Nicolas Sahakian, Pauline RomanetAnnales D'Endocrinologie|February 7, 2024
Updates on the genetics of multiple endocrine neoplasiaNicolas Sahakian, Frederic Castinetti, Pauline Romanet, et al.Frontiers in Endocrinology|October 14, 2024
Challenges in molecular diagnosis of multiple endocrine neoplasiaPauline Romanet, Théo Charnay, Nicolas Sahakian, et al.Pediatrics|March 25, 2015
Case report of GNAS epigenetic defect revealed by a congenital hypothyroidismPauline Romanet, Lindsay Osei, Irène Netchine, et al.Annales D'Endocrinologie|January 16, 2025
Chapter 5: The roles of genetics in primary hyperparathyroidismPauline Romanet, Lucie Coppin, Arnaud Molin, et al.The Gulf Journal of Oncology|June 11, 2026
De novo mutation of the RET proto-oncogene revealing multiple endocrine neoplasia type 2A: a sporadic case from Western AlgeriaAmina Chami, Pauline Romanet, Fatima Mohammedi, et al.Clinics and Research in Hepatology and Gastroenterology|June 28, 2011
Pitfall of hepatitis B surface antigen testing in a kidney transplant recipient presenting hepatitis B reactivationPauline Romanet, Henri Vacher-Coponat, Valérie Moal, et al.Clinical Endocrinology|December 16, 2024
CSNK2B Mutation: A Rare Cause of IGHDKarine Aouchiche, Pauline Romanet, Anne Barlier, et al.Journal of Clinical Medicine|May 24, 2018
Functioning Mediastinal Paraganglioma Associated with a Germline Mutation of von Hippel-Lindau GeneThibault Bahougne, Pauline Romanet, Amira Mohamed, et al.Pageof 6