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Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Congenital hypothyroidism with gland in situ: diagnostic re-evaluation 1-gen-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 1-gen-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 1-gen-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 1-gen-2014 M.C. VigoneF. Mosca + Article (author) -
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn from Discordant Twins 1-gen-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 1-gen-2020 Fugazzola, LauraVigone, Maria CristinaPersani, Luca + Article (author) -
Mostrati risultati da 1 a 6 di 6
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