WEBER, GIOVANNA

WEBER, GIOVANNA  

Facoltà di Medicina e Chirurgia  

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Risultati 1 - 20 di 222 (tempo di esecuzione: 0.018 secondi).
Titolo Data di pubblicazione Autore(i) File
"Block-and-replace" method in pediatric Graves' disease 1-gen-2012 Vigone, Mc; Peroni, E; Passoni, A; Tronconi, Gm; Rabbiosi, S; Chiumello, G; Weber, Giovanna
"Effect of long-term glucocorticoid therapy on bone density and bone remodeling indexes in patients with congenital adrenal hyperplasia" 1-gen-1995 Mora, S.; Weber, Giovanna; Saggion, F.; Russo, G.; Prinster, C.; Proverbio, M. C.; Chiumello, G.
A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH) 1-gen-2009 Corbetta, C; Weber, Giovanna; Cortinovis, F; Calebiro, D; Passoni, A; Vigone, Mc; Beck Peccoz, P; Chiumello, G; Persani, L.
A case of metabolic syndrome in an adolescent: diagnosis and management 1-gen-2009 Cammarata, B; Frontino, G; Biffi, V; Viscardi, M; Di Candia, S; Weber, Giovanna
A frequent oligogenic involvement in congenital hypothyroidism 1-gen-2017 de Filippis, Tiziana; Gelmini, Giulia; Paraboschi, Elvezia; Vigone, Maria Cristina; Di Frenna, Marianna; Marelli, Federica; Bonomi, Marco; Cassio, Alessandra; Larizza, Daniela; Moro, Mirella; Radetti, Giorgio; Salerno, Mariacarolina; Ardissino, Diego; Weber, Giovanna; Gentilini, Davide; Guizzardi, Fabiana; Duga, Stefano; Persani, Luca
A new mutation in AVPR2 gene discovered in an infant with nephrogenic diabetes insipidus 1-gen-2005 Marenzi, K; Di Candia, S; Noè, A; Passoni, A; Frugnoli, I; Torre, G; Faà, V; Weber, Giovanna; Chiumello, G.
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism 1-gen-2001 Alberti, L; Proverbio, Mc; Costagliola, S; Weber, Giovanna; BECK PECCOZ, P; Chiumello, G; Persani, L.
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis 1-gen-2008 Muzza, M; Persani, L; de Filippis, T; Gastaldi, R; Vigone, Mc; Sala, D; Weber, Giovanna; Lorini, R; Beck Peccoz, P; Fugazzola, L.
Accidental exposure to polychlorinated biphenyls in a farm 1-gen-2005 Di Candia, S; Odoni, M; Guarneri, Mp; Cortinovis, F; Mora, S; Weber, Giovanna; Chiumello, G.
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches 1-gen-2001 Corrias, A; Einaudi, S; Chiorboli, E; Weber, Giovanna; Crin, A; Andreo, M; Cesaretti, G; DE SANCTIS, L; Messina, Mf; Segni, M; Cicchetti, M; Vigone, M; Pasqioni, Am; Spera, S; DE LUCA, F; Mussa, Gc; Bona, G.
Allungamento chirurgico degli arti: in quali casi intervenire? A che età iniziare? 1-gen-1988 Bregani, P; Weber, Giovanna; Turba, F; Peretti, G; Morandi, A; Chiumello, G.
Alternative diagnostic approach to the etiology definition of Congenital Hypothyroidism" 1-gen-1995 Siragusa, V.; Vigone, M. C.; Paesano, P. L.; Dosio, F.; Mora, S.; Weber, Giovanna; Rondanini, G. F.; DEL MASCHIO, Alessandro; Fazio, F.; Chiumello, G.
Analysis of 21-deoxycortisol, a marker of congenital adrenal hyperplasia, in blood by atmospheric pressure chemical ionization and electrospray ionization using multiple reaction monitoring 1-gen-2004 Cristoni, S; Cuccato, D; Sciannamblo, M; Bernardi, Lr; Biunno, I; Gerthoux, P; Russo, G; Weber, Giovanna; Mora, S.
Analysis of TSH Receptor gene in four cases with the clinical features of partial TSH resistance" 1-gen-1999 Romoli, R.; Persani, L.; Proverbio, M. C.; Asteria, C.; Vigone, C.; Weber, Giovanna; Beck Peccoz, P.
Anterior pituitary gland aplasia: neuroradiological, phenotypical and hormonal evaluation 1-gen-2013 Damia, Cm; Ferrarello, Mp; Pozzobon, G; Cannalire, G; Voto, A; Garbetta, G; Osimani, S; Weber, Giovanna
Asymptomatic Thyrotropin-secreting Pituitary Macroadenoma in a Thirteen Year-old Girl: Successful First-line Treatment with Somatostatin Analogues 1-gen-2012 Rabbiosi, S; Peroni, E; Tronconi, Gm; Chiumello, G; Losa, M; Weber, Giovanna
Attention abilities in preadolescents and adolescents with congenital hypothyroidism 1-gen-2009 Colombini, Mi; Pozzi, C; Vigone, Mc; Passoni, A; Cortinovis, F; Rabbiosi, S; Maina, L; Weber, Giovanna; Chiumello, G.
Autosomal dominant hypocalcemia in monozygotic twins caused by a de novo germline mutation near the amino-terminus of the human calcium receptor 1-gen-2004 Hu, J; Mora, S; Weber, Giovanna; Zamproni, I; Proverbio, Mc; Spiegel, Am
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome 1-gen-2006 Vezzoli, G; Arcidiacono, T; Terranegra, A; Biasion, R; Weber, G; Mora, S; Syren, Ml; Coviello, D; Cusi, D; Bianchi, G; Soldati, L; Paloschi, V; Soldati, L.
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism 1-gen-2008 Zamproni, I; Grasberger, H; Cortinovis, F; Vigone, Mc; Chiumello, G; Mora, S; Onigata, K; Fugazzola, L; Refetoff, S; Persani, L; Weber, Giovanna