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Alberto Falchetti

Showing results (91-100 of 102) with videos related to

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Endocrine|January 29, 2020
Prediction of hypertension, diabetes and fractures in eucortisolemic women by measuring parameters of cortisol milieuValentina Morelli, Carmen Aresta, Agostino Gaudio, et al.
Aging Clinical and Experimental Research|December 1, 2010
LRP5 gene polymorphism and cortical boneFulvio Lauretani, Chiara Cepollaro, Stefania Bandinelli, et al.
Calcified Tissue International|December 11, 2008
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 boneAlberto Falchetti, Marco Di Stefano, Francesca Marini, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 1, 2021
Management of bone fragility in type 2 diabetes: Perspective from an interdisciplinary expert panelIacopo Chiodini, Agostino Gaudio, Andrea Palermo, et al.
Endocrine|February 11, 2025
Phosphate metabolism in primary hyperparathyroidism: a real-life long-term studyCarla Columbu, Domenico Rendina, Luigi Gennari, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 6, 2004
Two novel mutations at exon 8 of the Sequestosome 1 (SQSTM1) gene in an Italian series of patients affected by Paget's disease of bone (PDB)Alberto Falchetti, Marco Di Stefano, Francesca Marini, et al.
European Journal of Endocrinology|June 3, 2010
Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypesCristina Romei, Stefano Mariotti, Laura Fugazzola, et al.
Nature Genetics|May 31, 2011
Genome-wide association identifies three new susceptibility loci for Paget's disease of boneOmar M E Albagha, Sachin E Wani, Micaela R Visconti, et al.
Plos Medicine|February 16, 2006
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS studyStuart H Ralston, André G Uitterlinden, Maria Luisa Brandi, et al.
Global & Regional Health Technology Assessment|July 28, 2025
Micro-costing analysis from Italian Guidelines for the management of sporadic primary hyperparathyroidismValentini Ilaria, Michele Basile, Fabio Vescini, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Endocrine|January 29, 2020
Prediction of hypertension, diabetes and fractures in eucortisolemic women by measuring parameters of cortisol milieuValentina Morelli, Carmen Aresta, Agostino Gaudio, et al.
Aging Clinical and Experimental Research|December 1, 2010
LRP5 gene polymorphism and cortical boneFulvio Lauretani, Chiara Cepollaro, Stefania Bandinelli, et al.
Calcified Tissue International|December 11, 2008
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 boneAlberto Falchetti, Marco Di Stefano, Francesca Marini, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 1, 2021
Management of bone fragility in type 2 diabetes: Perspective from an interdisciplinary expert panelIacopo Chiodini, Agostino Gaudio, Andrea Palermo, et al.
Endocrine|February 11, 2025
Phosphate metabolism in primary hyperparathyroidism: a real-life long-term studyCarla Columbu, Domenico Rendina, Luigi Gennari, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 6, 2004
Two novel mutations at exon 8 of the Sequestosome 1 (SQSTM1) gene in an Italian series of patients affected by Paget's disease of bone (PDB)Alberto Falchetti, Marco Di Stefano, Francesca Marini, et al.
European Journal of Endocrinology|June 3, 2010
Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypesCristina Romei, Stefano Mariotti, Laura Fugazzola, et al.
Nature Genetics|May 31, 2011
Genome-wide association identifies three new susceptibility loci for Paget's disease of boneOmar M E Albagha, Sachin E Wani, Micaela R Visconti, et al.
Plos Medicine|February 16, 2006
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS studyStuart H Ralston, André G Uitterlinden, Maria Luisa Brandi, et al.
Global & Regional Health Technology Assessment|July 28, 2025
Micro-costing analysis from Italian Guidelines for the management of sporadic primary hyperparathyroidismValentini Ilaria, Michele Basile, Fabio Vescini, et al.
Pageof 11