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Annales D'Endocrinologie|May 8, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
Annales D'Endocrinologie|March 21, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
The Journal of Clinical Endocrinology and Metabolism|July 29, 2022
Early Detection of Relapse by ctDNA Sequencing in a Patient with Metastatic Thymic Tumor and MEN1 MosaicismArnaud Lagarde, Lauriane Le Collen, Camille Boulagnon, et al.
European Journal of Nuclear Medicine and Molecular Imaging|September 18, 2017
Quantitative 18F-DOPA PET/CT in pheochromocytoma: the relationship between tumor secretion and its biochemical phenotypeVincent Amodru, Carole Guerin, Sarkis Delcourt, et al.
European Journal of Endocrinology|January 12, 2026
Histological Evidence of familial GH-PitNET Associated with Germline MAX MutationLaurence Salle, Alexandre Buffet, Gérald Raverot, et al.
Pituitary|December 9, 2025
From misclassified AIP variant to carney complex: a case report and retrospective evaluation of PRKAR1A in pituitary tumor predispositionCécilia Piazzola, Lauriane Le Collen, Théo Charnay, et al.
Clinical Endocrinology|September 4, 2019
Exploring the link between tumour metabolism and succinate dehydrogenase deficiency: A 18 F-FDOPA PET/CT study in head and neck paragangliomasThibaut Reichert, Nicolas Fakhry, Jean-Pierre Lavieille, et al.
Endocrine Pathology|November 14, 2016
Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX MutationPauline Romanet, Carole Guerin, Pascal Pedini, et al.
European Journal of Human Genetics : EJHG|September 29, 2018
Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiencyNicolas Jullien, Pauline Romanet, Mélanie Philippon, et al.
European Journal of Endocrinology|July 5, 2020
Germinal defects of SDHx genes in patients with isolated pituitary adenomaGrégory Mougel, Arnaud Lagarde, Frédérique Albarel, et al.
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