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Titolo Data di pubblicazione Autori Tipo File Abstract
Congenital hypothyroidism with gland in situ: diagnostic re-evaluation 2005 G. WeberM.C. VigoneM.C. ProverbioL. PersaniG. Chiumello + Article (author) -
Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy 2007 L. FugazzolaL. PersaniG. VannucchiD. MannavolaM.C. VigoneG. WeberP. Beck-Peccoz + Article (author) -
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia 2012 D. CordellaM. BonomiD.V. LibriM.C. VigoneP. Beck PeccozL. Persani + Article (author) -
Evolution of thyroid function in preterm infants detected by screening for congenital hypothyroidism 2014 M.C. VigoneF. Mosca + Article (author) -
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn from Discordant Twins 2019 Vigone M. C.Weber G.Gelmini G.Persani L. + Article (author) -
Congenital hypothyroidism: a 2020 consensus guidelines update An ENDO-EUROPEAN REFERENCE NETWORK (ERN) initiative endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology 2020 Fugazzola, LauraVigone, Maria CristinaPersani, Luca + Article (author) -
Unusual causes of hyperthyrotropinemia and differential diagnosis of primary hypothyroidism: a revised diagnostic flowchart 2023 Irene CampiMarco Dell’AcquaElisa Stellaria GrassiMaria Cristina VigoneLuca Persani Article (author) -
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