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Copeptin assays in children for the differential diagnosis of polyuria‐polydipsia syndrome and reference levels in hospitalized children

Archive ouverte | Bonnet, Laura | CCSD

International audience

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Archive ouverte | Perreard, Pauline | CCSD

International audience. ObjectiveThe aim of this study was to describe the quality of life (QoL) of children with a chronic illness treated in a tertiary multidisciplinary pediatric department in comparison with the...

Congenital Central Hypothyroidism Caused by a Novel IGSF1 Variant Identified in a French Family

Archive ouverte | Fourneaux, Rachel | CCSD

International audience. Introduction: Congenital central hypothyroidism (CCH) is a rare disorder that can be caused by X-linked mutations in the immunoglobulin superfamily member 1 (IGSF1) gene. Here, we describe fo...

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