Sfoglia per Autore
Two novel nonsense mutations in GALNT3 gene are responsible for familial tumoral calcinosis
2007 A.M. Barbieri, M. Filopanti, G. Bua, P. Beck-Peccoz
Patients with macroprolactinaemia : clinical and radiological features
2007 F. Donadio, A. Barbieri, R. Angioni, G. Mantovani, P. Beck-Peccoz, A. Spada, A.G. Lania
The role of midnight salivary cortisol levels in the diagnosis of subclinical hypercortisolism (SH) in patients with adrenal incidentaloma
2008 B. Masserini, S. Bergamaschi, A.M. Barbieri, A. Salcuni, V. Morelli, A. Scillitani, P. Beck-Peccoz, I. Chiodini
Eukaryotic initiation factor 6 is rate-limiting in translation, growth and transformation
2008 V. Gandin, A. Miluzio, A.M. Barbieri, A. Beugnet, H. Kiyokawa, P.C. Marchisio, S. Biffo
Dopamine D2 receptor gene polymorphisms and response to cabergoline therapy in patients with prolactin-secreting pituitary adenomas
2008 M. Filopanti, A.M. Barbieri, A.R. Angioni, A. Colao, V. Gasco, S. Grottoli, A. Peri, S. Baglioni, M.F. Fustini, F. Pigliaru, P.D. Monte, G. Borretta, B. Ambrosi, M.L. Jaffrain Rea, M. Gasperi, S. Brogioni, S. Cannavò, G. Mantovani, P. Beck Peccoz, A. Lania, A. Spada
Peripheral insulin-like factor 3 concentrations are reduced in men with type 2 diabetes mellitus : effect of glycemic control and visceral adiposity on Leydig cell function
2009 F. Ermetici, F. Donadio, L. Iorio, A.E. Malavazos, A. Dolci, E. Peverelli, A.M. Barbieri, L. Morricone, I. Chiodini, M. Arosio, A. Lania, P. Beck Peccoz, B. Ambrosi, S. Corbetta
The limited role of midnight salivary cortisol levels in the diagnosis of subclinical hypercortisolism in patients with adrenal incidentaloma
2009 B. Masserini, V. Morelli, S. Bergamaschi, F. Ermetici, C. Eller-Vainicher, A.M. Barbieri, M.A. Maffini, A. Scillitani, B. Ambrosi, P. Beck Peccoz, I. Chiodini
The effect of calcimimetic R-568 on the functional role of the calcium-sensing receptor R990G polymorphism
2010 A. Terranegra, A. Ferraretto, E. Dogliotti, S.L. Corbetta, M. Scarpellini, A.M. Barbieri, A. Spada, T. Arcidiacono, F. Rainone, A. Aloia, D.M. Cusi, G. Vezzoli, L. Soldati
Pseudohypoparathyroidism and GNAS epigenetic defects : clinical evaluation of Albright hereditary osteodystrophy and molecular analysis in 40 patients
2010 G. Mantovani, L. de Sanctis, A.M. Barbieri, F.M. Elli, V. Bollati, V. Vaira, P. Labarile, S. Bondioni, E.M. Peverelli, A.G.A. Lania, P.L.M. Beck Peccoz, A. Spada
Calcimimetic R-568 effects on activity of R990G polymorphism of calcium-sensing receptor
2010 A. Terranegra, A. Ferraretto, E. Dogliotti, M. Scarpellini, S.L. Corbetta, A.M. Barbieri, A. Spada, T. Arcidiacono, F. Rainone, A. Aloia, D.M. Cusi, G. Vezzoli, L. Soldati
Pharmacology of the calcium sensing receptor
2013 M. Filopanti, S. Corbetta, A.M. Barbieri, A. Spada
Pseudohypoparathyroidism Type Ia and Pseudo-Pseudohypoparathyroidism : The Growing Spectrum of GNAS Inactivating Mutations
2013 F.M. Elli, L. Desanctis, B. Ceoloni, A.M. Barbieri, P. Bordogna, P. Beck Peccoz, A. Spada, G. Mantovani
Pseudohypoparathyroidism type Ia : a novel GNAS mutation in a Brazilian boy presenting with an early primary hypothyroidism
2013 C. Alves, S. Sampaio, A.M. Barbieri, G. Mantovani
Screening for GNAS genetic and epigenetic alterations in progressive osseous heteroplasia : first Italian series
2013 F.M. Elli, A. Barbieri, P. Bordogna, P. Ferrari, R. Bufo, E. Ferrante, E. Giardino, P. Beck Peccoz, A. Spada, G. Mantovani
Role of UGT1A1 and ADH gene polymorphisms in pegvisomant-induced liver toxicity in acromegalic patients
2014 M. Filopanti, A.M. Barbieri, G. Mantovani, S. Corbetta, V. Gasco, M. Ragonese, C. Martini, F. Bogazzi, A. Colao, D. Ferone, A. Peri, F. Pigliaru, G. Angeletti, M. Arosio, P. Beck-Peccoz, A.G. Lania, A. Spada
Impact of IGF(CA)19 gene polymorphism on the metabolic response to GH therapy in adult GH-deficient patients
2014 C. Giavoli, E. Profka, E. Sala, M. Filopanti, A.M. Barbieri, S. Bergamaschi, E. Ferrante, M. Arosio, B. Ambrosi, A.G. Lania, A. Spada, P. Beck-Peccoz
Quantitative analysis of methylation defects and correlation with clinical characteristics in patients with pseudohypoparathyroidism type I and GNAS epigenetic alterations
2014 F.M. Elli, L. De Sanctis, V. Bollati, L. Tarantini, M. Filopanti, A.M. Barbieri, E. Peverelli, P. Beck-Peccoz, A. Spada, G. Mantovani
Role of IGF1-(CA)19 promoter microsatellite in the clinical presentation of acromegaly
2014 E. Sala, M. Filopanti, E. Ferrante, A.M. Barbieri, E. Malchiodi, E. Verrua, C. Giavoli, A.G. Lania, M. Arosio, P. Beck-Peccoz, A. Spada, G. Mantovani
In postmenopausal female subjects with type 2 diabetes mellitus, vertebral fractures are independently associated with cortisol secretion and sensitivity
2015 V.V. Zhukouskaya, C. Eller-Vainicher, A. Gaudio, E. Cairoli, F.M. Ulivieri, S. Palmieri, V. Morelli, E. Orsi, B. Masserini, A.M. Barbieri, E. Polledri, S. Fustinoni, A. Spada, C.E. Fiore, I. Chiodini
Bone involvement and mineral metabolism in Williams’ syndrome
2018 S. Palmieri, M.F. Bedeschi, E. Cairoli, V. Morelli, M.E. Lunati, A. Scillitani, V. Carnevale, F. Lalatta, A.M. Barbieri, E. Orsi, A. Spada, I. Chiodini, C. Eller-Vainicher
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