Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Antonietta Amedei"'
1
A patient with MEN1-associated hyperparathyroidism, responsive to cinacalcet
Autor: Alberto, Falchetti, Antonio, Cilotti, Luca, Vaggelli, Luca, Vagelli, Laura, Masi, Antonietta, Amedei, Federica, Cioppi, Francesco, Tonelli, Maria Luisa, Brandi
Publikováno v: Nature Clinical Practice Endocrinology & Metabolism. 4:351-357
The patient described in this article had a history of hereditary primary hyperparathyroidism, which is usually treated surgically. When the patient developed a recurrent parathyroid adenoma she refused surgery and in this Case Study the authors desc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b561c2d4e3c2f769872816b1e63ff066
https://doi.org/10.1038/ncpendmet0816
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2
Polymorphism of the Aromatase Gene in Postmenopausal Italian Women: Distribution and Correlation with Bone Mass and Fracture Risk1
Autor: Emanuela Colli, Alberto Falchetti, Antonietta Amedei, Maria Luisa Brandi, Maria Farci, Sandra Silvestri, L. Becherini, Luigi Gennari, Stefano Gonnelli, Laura Masi
Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 86:2263-2269
Conversion of C19 steroids to estrogens is catalyzed by the aromatase enzyme. Inactivating mutations of the aromatase gene are associated with decreased bone mineral density in both men and women. Genetic studies suggest that several genes contribute
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::17f8d4fb106faa0aceaef7442e25b0e9
https://doi.org/10.1210/jcem.86.5.7450
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3
The role of osteoprotegerin (OPG) and estrogen receptor (ER-α) gene polymorphisms in rheumatoid arthritis
Autor: Laura, Masi, Susanna, Maddali Bongi, Chiara, Angotti, Francesca, Del Monte, Silvia, Carbonell Sala, Massimo, Basetti, Antonietta, Amedei, Alberto, Falchetti, Maria Luisa, Brandi
Publikováno v: Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases. 4(2)
Objective. Osteoclast activation at the cartilage pannus junction is an essential step in the destruction of bone matrix in patients affected by rheumatoid arthritis (RA). Receptor activator of NFkappaB ligand (RANK-L) is responsible for osteoclast d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::aa73b9aba25ac5bdfdd15347f1909d02
https://pubmed.ncbi.nlm.nih.gov/22461216
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4
Fracture unit: a (possible) model of implementation in Italy
Autor: Alberto, Falchetti, Antonietta, Amedei, Laura, Masi, Francesca, Giusti, Loredana, Cavalli, Cristiana, Casentini, Maria Luisa, Brandi
Publikováno v: Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases. 8(1)
The "Fracture Unit" is one of the possible answers to the advanced health needs of the growing number of elderly in our Country, aimed at achieving effective and efficient management of fracture events due to osteoporosis or fragility fractures. Here
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7dd1e5f53312addd050d9d4dbc625b53
https://pubmed.ncbi.nlm.nih.gov/22461796
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5
The bone care nurse project
Autor: Cristiana, Casentini, Giuseppe, Chiaramonti, Antonietta, Amedei, Federica, Cioppi, Alberto, Falchetti, Laura, Masi, Maria Luisa, Brandi
Publikováno v: Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases. 8(1)
In today's society, citizens are called to play an increasingly active role in decision planning related to the various aspects of work, social and political life. This trend has been also confirmed in the health’s field. In fact, the citizen is al
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5f363403309963a9a5e9322dcf33aba0
https://pubmed.ncbi.nlm.nih.gov/22461806
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6
Genetic aspects of the Paget's disease of bone: concerns on the introduction of DNA-based tests in the clinical practice. Advantages and disadvantages of its application
Autor: Alberto, Falchetti, Falchetti, Alberto, Francesca, Marini, Marini, Francesca, Laura, Masi, Masi, Laura, Antonietta, Amedei, Amedei, Antonietta, Maria Luisa, Brandi, Brandi Maria, Luisa
Publikováno v: European journal of clinical investigation. 40(7)
A large amount of genetic studies have clearly demonstrated the existence of a genetic susceptibility to Paget's disease of bone (PDB). Although the disease is genetically heterogeneous, the SQSTM1/p62 gene, encoding a protein with a pathophysiologic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fdaf3eb2cccebbb21a3c197f774bea94
https://pubmed.ncbi.nlm.nih.gov/20658751
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7
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)
Autor: Susanna Maddali Bongi, Federica Cioppi, Laura Masi, Maria Laura De Feo, Carmelo Mavilia, G.C. Isaia, Giuseppina Di Fede, Antonietta Amedei, Debora Strigoli, Marco Matucci-Cerinic, Valentina Ghinoi, Alberto Falchetti, Giovan Battista Rini, Daniela Melchiorre, Maria Luisa Brandi, C. Sferrazza, Francesca Del Monte, Francesca Marini, Marco Di Stefano
Publikováno v: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 19(6)
PDB is genetically heterogeneous. Mutations of the sequestosome1 gene have been reported in sporadic and familial forms of Paget's in patients of French Canadian and British descent. Mutational analyses in different ethnic groups are needed to accura
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f94f760a0375f8057b88dfa9828a2171
https://pubmed.ncbi.nlm.nih.gov/15125799
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9
[Untitled]
Autor: Alberto Falchetti, Antonietta Amedei, Giancarlo Isaia, Alessia Gozzini, Annamaria Carossino, Francesca Del Monte, Maria Luisa Brandi, Francesca Marini, Annalisa Tanini, Laura Masi, Marco Di Stefano
Publikováno v: Arthritis Research & Therapy. 7:R1289
Mutations of the p62/Sequestosome 1 gene (p62/SQSTM1) account for both sporadic and familial forms of Paget's disease of bone (PDB). We originally described a methionine→valine substitution at codon 404 (M404V) of exon 8, in the ubiquitin protein-b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fd4e45d808bc4b719b3dc4c692643d66
https://doi.org/10.1186/ar1828
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10
Akademický článek
Genetic aspects of the Paget's disease of bone: concerns on the introduction of DNA-based tests in the clinical practice. Advantages and disadvantages of its application.
Autor: Falchetti A; Regional Center for Hereditary Endocrine Tumors, Unit of Metabolic Bone Diseases, AOUC, Department of Internal Medicine, University of Florence, Florence, Italy., Marini F, Masi L, Amedei A, Brandi ML
Publikováno v: European journal of clinical investigation [Eur J Clin Invest] 2010 Jul; Vol. 40 (7), pp. 655-67.
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