MANNAVOLA, DEBORAH ELENA

MANNAVOLA, DEBORAH ELENA  

DIPARTIMENTO DI SCIENZE MEDICHE (attivo dal 01/01/2000 al 27/04/2012)  

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Risultati 1 - 20 di 20 (tempo di esecuzione: 0.016 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
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) -
A novel tyrosine-kinase selective inhibitor, sunitinib, induces transient hypothyroidism by blocking iodine uptake 2007 D. MannavolaG. M. VannucchiP.G. CasaliP. Beck-PeccozL. Fugazzola + Article (author) -
Analysis of a deiodinase 2 polymorphism (oRFa-Asp) in patients with Graves’ disease and controls : preliminary results 2006 G. VannucchiD. MannavolaV. CirelloI. CampiM. MuzzaP. Beck-PeccozL. Fugazzola Article (author) -
Syndromes of hormone resistance in the hypothalamic-pituitary-thyrod axis 2006 P. Beck-PeccozL. PersaniD. CalebiroM. BonomiD. MannavolaI. Campi Article (author) -
Correlation between B-RAF(V600E) mutation and clinico-pathologic parameters in papillary thyroid carcinoma: data from a multicentric Italian study and review of the literature 2006 L. FugazzolaV. CirelloD. MannavolaP. Beck-Peccoz + Article (author) -
TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature 2006 D. MannavolaG. VannucchiL. FugazzolaV. CirelloI. CampiL. PersaniP. Beck-Peccoz + Article (author) -
Gitelman’s sindrome : description of a new case in a family with RTH 2005 D. MannavolaG. VannucchiL. FugazzolaM. PerrinoV. CirelloM. MuzzaP. Beck Peccoz Article (author) -
Total iodide organification defect : clinical and molecular characterization of an Italian family 2005 L. FugazzolaD. MannavolaV. CirelloP. Beck-PeccozL. Persani + Article (author) -
Syndromes of thyroid hormone resistance 2005 P. Beck-PeccozD. MannavolaL.Persani Article (author) -
Radioiodine treatment of non-toxic multinodular goitre : effects of combination with lithium 2005 G. VannucchiD. MannavolaP. Beck-PeccozL. Fugazzola + Article (author) -
Different responses to chronic somatostatin analogues in patients with central hyperthyroidism 2005 D. MannavolaL. PersaniG. VannucchiL. FugazzolaP. Beck-Peccoz + Article (author) -
BRAF mutations in an Italian series of thyroid cancers 2004 L. FugazzolaD. MannavolaV. CirelloG. VannucchiM. MuzzaP. Beck-Peccoz + Article (author) -
A novel splice variant involving the 5’ untranslated region of thyroid hormone receptor beta1 (TRbeta1) 2004 D. MannavolaP. Beck-PeccozL. Persani + Article (author) -
A novel splice variant involving the 5’ untranslated region of thyroid hormone receptor β1 (TRβ1) 2004 D. MannavolaP. Beck-PeccozL. Persani + Article (author) -
Absence of BRAF mutations in endocrine tumors 2004 D. MannavolaV. CirelloM. MuzzaP. Beck-PeccozL. Fugazzola Article (author) -
Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defect 2003 L. FugazzolaN. CeruttiD. MannavolaG. VannucchiC. FalliniL. PersaniP. Beck-Peccoz Article (author) -
Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during L-thyroxine replacement 2003 L. FugazzolaL. PersaniD. MannavolaG. VannucchiP. Beck-Peccoz + Article (author) -
Syndromes of thyroid hormone resistance due to mutations in the T3[beta] receptor: progress in our understanding 2000 P. Beck-PeccozD. MannavolaL. Persani Article (author) -
Prenatal diagnosis of thyroid hormone resistance 1999 L. PersaniD. Mannavola + Article (author) -
Clinical and hormonal outcome after two years of triiodothyroacetic acid treatment in a child with thyroid hormone resistance 1997 L. PersaniD. MannavolaD. CortelazziP. Beck-Peccoz + Article (author) -