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Archive ouverte | Cuny, Thomas | CCSD

International audience. Context: Familial hypocalciuric hypercalcemia type 1 (FHH-1) defines an autosomal dominant disease, related to mutations in the CASR gene, with mild hypercalcemia in most cases. Cases of FHH...

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Archive ouverte | Boucher, Aymeric | CCSD

International audience. PurposeThe aims of the study were to evaluate the performance and robustness of [18F]fluorocholine PET/CT in detecting hyperfunctioning parathyroid glands in MEN1-related primary hyperparathy...

Correction to: MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectives

Archive ouverte | Amodru, Vincent | CCSD

International audience

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