Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Federica, Cioppi"'
Publikováno v:
Endocrine Connections, Vol 11, Iss 5, Pp 1-12 (2022)
Multiple endocrine neoplasia type 1 (MEN1) is a rare, inherited cancer syndrome characterized by the development of multiple endocrine and non-endocrine tumors. MEN1 patients show a reduction of bone mass and a higher prevalence of early onset osteop
Externí odkaz:
https://doaj.org/article/0c777d5447254a5f972a5366edc01390
Autor:
Francesca Giusti, Federica Cioppi, Caterina Fossi, Francesca Marini, Laura Masi, Francesco Tonelli, Maria Luisa Brandi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Abstract Background MEN1 is a complex, rare, syndrome inherited in an autosomal dominant tract and characterized by the development of multiple neuroendocrine tumors, requiring lifelong surveillance and multiple medical and surgical therapies through
Externí odkaz:
https://doaj.org/article/56fd11c71a6d4e5fb557bcf613968d65
Autor:
Francesca Marini, Francesca Giusti, Federica Cioppi, Davide Maraghelli, Tiziana Cavalli, Francesco Tonelli, Maria Luisa Brandi
Publikováno v:
Cells, Vol 10, Iss 8, p 1895 (2021)
Primary hyperparathyroidism (PHPT) is the most common endocrinopathy in multiple endocrine neoplasia type 1 (MEN1). Persistent levels of increased parathyroid hormone (PTH) result in a higher incidence of osteopenia and osteoporosis compared to the g
Externí odkaz:
https://doaj.org/article/3f71393f5b0848a1a4862b8015d3bffe
Autor:
Francesca Giusti, Federica Cioppi, Caterina Fossi, Francesca Marini, Laura Masi, Francesco Tonelli, Maria Luisa Brandi
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 107:e2110-e2123
Context Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited endocrine cancer syndrome. Multiple gastro-entero-pancreatic neuroendocrine tumors (GEP-NETs) affect 30% to 80% of MEN1 patients, with the most common functioning GEP-NET being ga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::603643645f21614b8867e3b3ab0ed40f
https://doi.org/10.1210/clinem/dgab903
https://doi.org/10.1210/clinem/dgab903
Autor:
Francesca Giusti, Federica Cioppi, Caterina Fossi, Francesca Marini, Laura Masi, Francesco Tonelli, Maria Luisa Brandi
Publikováno v:
International Journal of Bone Fragility. 1:87-91
Purpose: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant cancer syndrome characterized by the development of multiple neuroendocrine tumors. The condition requires lifelong surveillance and multiple medical and surgical therap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f44a850c85e2090e181b6fd9257c2c61
https://doi.org/10.57582/ijbf.210102.087
https://doi.org/10.57582/ijbf.210102.087
Autor:
Marini, Francesca, Laura, Masi, Giusti, Francesca, Cianferotti, Luisella, Federica, Cioppi, Marcucci, Gemma, Simone, Ciuffi, Emmanuel, Biver, Giuseppe, Toro, Giovanni, Iolascon, Iantomasi, Teresa, and Maria Luisa Brandi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______310::24c95480c9df8f1f96bb2de15cc9956d
http://hdl.handle.net/2158/1257146
http://hdl.handle.net/2158/1257146
Autor:
Francesca Marini, Laura Masi, Francesca Giusti, Luisella Cianferotti, Federica Cioppi, Gemma Marcucci, Simone Ciuffi, Emmanuel Biver, Giuseppe Toro, Giovanni Iolascon, Teresa Iantomasi, Maria Luisa Brandi
Context Hypophosphatasia (HPP) is a rare metabolic disorder caused by deficiency of alkaline phosphatase (ALP) enzyme activity, leading to defective mineralization, due to pathogenic variants of the ALPL gene, encoding the tissue nonspecific alkaline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53e1099e24b5d88d2316a8da1d08606b
http://hdl.handle.net/11591/459124
http://hdl.handle.net/11591/459124
Autor:
Gemma Marcucci, M. L. Brandi, Federica Cioppi, Francesca Giusti, Luisella Cianferotti, Gigliola Leoncini, Francesca Marini, Francesco Franceschelli, Laura Masi, Giorgio Gronchi
Publikováno v:
Osteoporosis International
Summary We analyzed polymorphism of the ALPL gene in patients with low serum levels of tissue-nonspecific alkaline phosphatase (TNAP). The presence of three or more of the less frequent alleles of ALPL polymorphisms was associated with significantly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0adc2b566eb01aca0f98b602f5648ff9
https://pubmed.ncbi.nlm.nih.gov/34097127
https://pubmed.ncbi.nlm.nih.gov/34097127
Autor:
Stefania Zovato, Annamaria Colao, Caterina Fossi, Luisella Cianferotti, Federica Cioppi, Paola Loli, Giuseppe Opocher, Paolo Beck-Peccoz, Antongiulio Faggiano, Filomena Cetani, Anna Spada, Luca Persani, Fabiana Guizzardi, Francesca Boaretto, Francesco Tonelli, Diego Ferone, Alfredo Scillitani, Laura Masi, Claudio Marcocci, Paola Tomassetti, Francesca Giusti, Maria Luisa Brandi, Piero Ferolla, Francesca Marini, Maria Vittoria Davì, Giuseppe Fanciulli, Franco Mantero
Publikováno v:
Endocrine. 62(1)
The original version of this article unfortunately contained a mistake in Table 2. The table 2 was truncated in the original publication. The full table 2 is given below.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b9abe66687c2d669ac356aa6ec9f4a7
https://pubmed.ncbi.nlm.nih.gov/29497973
https://pubmed.ncbi.nlm.nih.gov/29497973
Publikováno v:
Familial Cancer. 15:133-138
Primary hyperparathyroidism (HPT) is the most common endocrinopathy in Multiple Endocrine Neoplasia type 1 (MEN1) syndrome. Supernumerary and/or ectopic parathyroid glands, potentially causes of persistent or recurrent HPT after surgery, have been pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46645595ac1e22c4cc1b64d726474786
https://doi.org/10.1007/s10689-015-9840-x
https://doi.org/10.1007/s10689-015-9840-x