Sfoglia per Autore  

Opzioni
Mostrati risultati da 61 a 80 di 97
Titolo Data di pubblicazione Autore(i) File
Phytoestrogen: food or drug? 2007 BACCIOTTINI L; FALCHETTI A; PAMPALONI B; BARTOLINI E; CAROSSINO A.M.; BRANDI M.L
The role of osteoprotegerin (OPG) and estrogen receptor (ER-α) gene polymorphisms in rheumatoid arthritis. 2007 L. Masi; S. Maddali Bongi; C. Angotti; F. Del Monte; S. Carbonell Sala; M. Bassetti; A. Amedei; A. Falchetti; M.L. Brandi
Is total parathyroidectomy the treatment of choice for hyperparathyroidism in multiple endocrine neoplasia type 1? 2007 F.Tonelli; T. Marcucci; G. Fratini; M. S. Tommasi; A. Falchetti; M.L. Brandi
Osteoporotic patient course after surgical treatment with hip prosthesis 2007 Roberto Monaco, Chiara Cepollaro, Gemma Marcucci, Rosario Imbriaco, Laura Masi, Alberto Falchetti, Gigliola Leoncini, Alessia Gozzini, Annalisa Tanini, Maria Luisa Brandi
FokI Polymorphisms of the Vitamin D Receptor Gene Correlates with Parameters of Bone Mass and Turnover in a Female Population of the Italian Island of Lampedusa. 2007 FALCHETTI A; SFERRAZZA C; CEPOLLARO C; GOZZINI A; DEL MONTE F; MASI L; NAPOLI N; DI FEDE G; CANNONE V; CUSUMANO G; PANDOLFO M.C; RINI G.B; TANINI A; M.L.BRANDI
Multiple endocrine neoplasms 2008 Falchetti A; Marini F; Luzi E; Tonelli F; Brandi ML.
A patient with MEN1-associated hyperparathyroidism, responsive to cinacalcet. 2008 A Falchetti; A Cilotti; L Vaggelli; L Masi; A Amedei; F Cioppi; F Tonelli; M L Brandi
Genetic Epidemiology of Paget's Disease of Bone in Italy: sequestosome1/p62 Gene Mutational Test and Haplotype Analysis at 5q35 in a Large Representative Series of Sporadic and Familial Italian Cases of Paget's Disease of Bone. 2008 A. Falchetti; M. Di Stefano; F. Marini; S. Ortolani; M. Ulivieri; S. Bergui; L. Masi; C. Cepollaro; M. Benucci; O. Di Munno; M. Rossini; S. Adami; A. Del Puente; G. Isaia; F. Torricelli; M. L. Brandi; On Behalf of
Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study. 2008 B. L. Langdahl; A. G. Uitterlinden; S. H. Ralston; T. A. Trikalinos; S. Balcells; M. L. Brandi; S. Scollen; P. Lips; R. Lorenc; B. Obermayer-Pietsch; D. M. Reid; J. B. Armas; P. P. Arp; A. Bassiti; M. Bustamante; L. B. Husted; A. H. Carey; R. P. Cano; H. Dobnig; A. M. Dunning; A. Fahrleitner-Pammer; A. Falchetti; E. Karczmarewicz; M. Kruk; J. P. T; L. Masi; J. B.; J. Mangion; F. E. A; L. Mellibovsky; L. Mosekilde; X. Nogués; H. A. P; J. Reeve; W. Renner; F. Rivadeneira; N. M. van; J. P. Joannidis; APOSS investigators; DOPS investigators; EPOS investigators; EPOLOS investigators; FAMOS investigators; LASA investigators; ERGO investigators; GENOMOS Study
Molecular genetic analysis in the diagnosis of humoral calcinosis 2008 Laura Masi, Alessia Gozzini, Antonietta Amedei, Alberto Falchetti, Gemma Marcucci, Annalisa Tanini, Maria Luisa Brandi
Modulatory effect of farnesyl pyrophosphate synthase (FDPS) rs2297480 polymorphism on the response to long-term amino-bisphosphonate treatment in postmenopausal osteoporosis 2008 F. Marini; A. Falchetti; S. Silvestri; Y. Bagger; E. Luzi; A. Tanini; C. Christiansen; M. L. Brandi
Characterisation of a Non-UBA Domain Missense Mutation of Sequestosome 1 (SQSTM1) in Paget's Disease of Bone. 2008 D. Najat; T. Garner; T. Hagen; B. Shaw; Paul W Sheppard; A. Falchetti; F. Marini; M. L. Brandi; J. E Long; J. R Cavey; Mark S Searle; R. Layfield
Biological effects of various regimes of 25-hydroxyvitamin D3 (calcidiol) administration on bone mineral metabolism in postmenopausal women 2009 Cavalli, Loredana; Cavalli, Tiziana; Marcucci, Gemma; Falchetti, Alberto; Masi, Laura; Brandi, Maria Luisa
Genotype-Phenotype Correlation Analyses in an Italian MEN1 Series. MEN1 Gene Mutational Performed at the Center for Hereditary Endocrine Tumors of Florence 2009 A. Falchetti;F. Giusti;F. Cioppi;L. Masi;A. Amedei;A. Cilotti;F. Marini;F. Tonelli;M. L. Brandi
Multiple endocrine neoplasia type I variants and phenocopies: more than a nosological issue? 2009 A. Falchetti; M. L. Brandi
A novel recessive mutation of fibroblast growth factor-23 in tumoral calcinosis 2009 L.Masi; A.Gozzini; A.Franchi; D.Campanacci; A.Amedei; A.Falchetti; F.Franceschelli; G.Marcucci; A.Tanini; R.Capanna; M.L.Brandi
Surgical approach in hereditary hyperparathyroidism. 2009 F. Tonelli;T. Marcucci;F. Giudici;A. Falchetti;M. L. Brandi
Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast-ovarian cancer syndromes: a case report. 2009 L.Papi; D.Palli; L.Masi; A.L.Putignano; C.Congregati; I.Zanna; F. Marini; F.Giusti; E.Luzi; F.Tonelli; M.Genuardi; M.L.Brandi; A.Falchetti
Multiple endocrine neoplasia type 1 (MEN1): not only inherited endocrine tumors. 2009 A. Falchetti;F. Marini;E. Luzi;F. Giusti;L. Cavalli;T. Cavalli;M. L. Brandi
DNA-based test: when and why to apply it to primary hyperparathyroidism clinical phenotypes 2009 A.Falchetti; F.Marini; F.Giusti; L.Cavalli; T.Cavalli; M.L.Brandi
Mostrati risultati da 61 a 80 di 97
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile