FRANCESCHELLI, FRANCESCO

FRANCESCHELLI, FRANCESCO  

Scienze Biomediche, Sperimentali e Cliniche 'Mario Serio'  

Mostra records
Risultati 1 - 20 di 38 (tempo di esecuzione: 0.018 secondi).
Titolo Data di pubblicazione Autore(i) File
A New Fgf23 Gene Polymorphism: Possible Role In the Pathogenesis of the Development of Extraskeletal Calcifications? 2013 G. Marcucci;L. Masi;F. Giusti;L. Cavalli;F. Franceschelli;G. Leoncini;C. Fossi;M. L. Brandi
A novel germline inactivating mutation in the CASR gene in an Italian kindred affected by familial hypocalciuric hypercalcemia. 2012 A. Falchetti; A. Gozzini; A. Terranegra; L. Soldati; G. Vezzoli; G. Leoncini; F. Giusti; F. Franceschelli; L. Masi; A. Tanini; L. Cavalli; 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
A NOVEL TISSUE-NONSPECIFIC ISOENZYME OF ALKALINE PHOSPHATASE (TNSALP) MUTATION IN ADULT PATIENT WITH LOW BONE MASS AND MUSCULOSKELETAL SYMPTOMS 2018 Masi, L; Franceschelli, F; Leoncini, G; Cioppi, F; Ottanelli, S; Marcucci, G; Giusti, F; Brandi, ML
Aromatase expression and activity in the human leukaemic cell line FLG 29.1. 1998 G. Fiorelli; U. Frediani; V. Martineti; A. Franchi; F. Gori; F. Franceschelli; A. Tanini; M. Serio; M. L. Brandi
CALCIFICATIONS IN DERMATOMYOSITIS: A CLINICAL CASE WITH AN ALTERATION OF PHOSPHATE HOMEOSTASIS, CARRIER OF A NEW FGF23 GENE MUTATION 2017 Masi, L; Marcucci, G; Giusti, F; Fossi, C; Franceschelli, F; Leoncini, G; Cioppi, F; Cianferotti, L; Brandi, L
Calcium bioavailability from a calcium-rich mineral water, with some observations on method. 2004 L. BACCIOTTINI; A. TANINI; A. FALCHETTI; L. MASI; F. FRANCESCHELLI; B. PAMPALONI; G. GIORGI; M.L. BRANDI
Can fibroblast growth factor (FGF)-23 circulating levels suggest coronary artery abnormalities in children with Kawasaki disease? 2013 L. Masi; F. Franceschelli; G. Leoncini; A. Gozzini; D. Rigante; F.L. Torre; M. Matucci Cerinic; M.L. Brandi; F. Falcini
Characterization, regulation, and function of specific cell membrane receptors for insulin-like growth factor I on bone endothelial cells. 1994 G. Fiorelli; C. Orlando; S. Benvenuti; F. Franceschelli; S. Bianchi; P. Pioli; A. Tanini; M. Serio; F. Bartucci; M. L. Brandi
Comparison of immuno- and HPLC-assays for the measurement of urinary collagen cross-links. 1994 CALABRESI E; L. LASAGNI; FRANCESCHELLI F; DE LEONARDIS V; BECORPI A; SERIO M; BRANDI ML
Correction of vitamin D status by calcidiol: pharmacokinetic profile, safety, and biochemical effects on bone and mineral metabolism of daily and weekly dosage regimens 2017 Minisola, S; Cianferotti, Luisella; Biondi, P; Cipriani, C; Fossi, Caterina; Franceschelli, Francesco; Giusti, Francesca; Leoncini, Gigliola; Pepe, J; Bischoff Ferrari, Ha; Brandi, MARIA LUISA
Effects of endothelin-1 on bovine parathyroid cells. 1993 A. Tanini; P. Failli; M. Maggi; F. Franceschelli; U. Frediani; L. Becherini; A. Giotti; C. Ruocco; M. L. Brandi
Effects of strontium on in vitro proliferation of human adipose tissue-derived mesenchymal stem cells. 2010 R.Zonefrati; G.Galli; C. Mavilia; F. Franceschelli; A.M. Carossino; V. Nardone; S. Fabbri; S. Ciuffi; A. Tanini; M.L. Brandi
Endothelin-1 increases intracellular calcium content in bovine parathyroid endothelial cells. 1992 P. Failli; C. Ruocco; A. Tanini; M. L. Brandi; S. Benvenuti; F. Franceschelli; A. Giotti
Fibroblast growth factor 23 (FGF23) gene polymorphism in children with Kawasaki syndrome (KS) and susceptibility to cardiac abnormalities. 2013 F. Falcini; D. Rigante; L. Masi; M. Covino; F. Franceschelli; G. Leoncini; G. Tarantino; M.M. Cerinic; M.L. Brandi
Genetic polymorphisms in uremic secondary hyperparathyroidism. 2002 L. GENNARI; L. BECHERINI; A. FALCHETTI; M. SALVADORI; A. TANINI; A. GOZZINI; F. FRANCESCHELLI; M. BRANDI; S. BANDINI; S. CARABELLESE; P. BORGATTI; T. LUSENTI; M. SURIAN; B. DOZIO; D. BRANCACCIO; P. CARPANI; F. VALLINO; E. CORGHI
Genetic polymorphisms in uremic secondary hyperparathyroidism. A multicentric Italian study 2001 GENNARI L; BECHERINI L; FALCHETTI A; BANDINI S; SALVATORI M; CARABELLESE S; BORGATTI P; LUCENTI T; SURIAN M; DOZIO B; BRANCACCIO D; CARPANI P; VALLINO F; CORGHI E; TANINI A; GOZZINI A; FRANCESCHELLI F; BRANDI M.L;
Genetic polymorphisms of vitamin D receptor and calcium sensing receptor gene in uremic secondary hyperparathyroidism: a multicentric italian study 2005 GENNARI L; FALCHETTI A; BANDINI S; CARABELLESE S; BORGATTI P; LUSENTI T; SURIAN M; DOZIO B; BRANCACCIO D; CARPANI P; VALLINO F; CORGHI E; A. TANINI; GOZZINI A; FRANCESCHELLI F; BRANDI M.L.
Genetics and pharmacogenetics of osteoporosis 2005 S. CARBONELL SALA; L. MASI; F. MARINI; F. DEL MONTE; A. FALCHETTI; F. FRANCESCHELLI; M.L. BRANDI
Human Preosteoblastic Cell Culture from a Patient with Severe Tumoral Calcinosis-Hyperphosphatemia Due to a New GALNT3 Gene Mutation: Study of In Vitro Mineralization. 2015 Masi, L; Beltrami, G; Ottanelli, S; Franceschelli, F; Gozzini, A; Zonefrati, R; Galli, G; Ciuffi, S; Mavilia, C; Giusti, F; Marcucci, G; Cioppi, F; Colli, E; Fossi, C; Franchi, A; Casentini, C; Capanna, R; Brandi, Ml