Zobrazeno 1 - 10
of 199
pro vyhledávání: '"Francesca, Giusti"'
Autor:
Francesca Marini, Francesca Giusti, Gaia Palmini, Cinzia Aurilia, Simone Donati, Maria Luisa Brandi
Publikováno v:
Endocrines, Vol 4, Iss 1, Pp 205-235 (2023)
Parathyroid carcinoma (PC) is a very rare endocrine cancer with aggressive behavior, a high metastatic potential, and a poor prognosis. Surgical resection of affected gland(s) and other involved structures is the elective therapy. Pre-operative and i
Externí odkaz:
https://doaj.org/article/a5f57f072a1e412ca4c6488930a3af7d
Autor:
Francesca Giusti
Publikováno v:
ArcHistoR Architettura Storia Restauro: Architecture History Restoration, Vol 0, Iss 18, Pp 140-161 (2023)
The paper focuses on an original aspect of the work of Georges Rohault de Fleury (1835-1904), who, from 1853 onwards, stayed in Pisa several times and for a long time to analyse medieval architecture and art, to which he dedicated about twenty years
Externí odkaz:
https://doaj.org/article/d1175d472834430f97db873c475f1913
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:
Angela Montanaro, Francesca Giusti, Matteo Zanfrognini, Paola Di Pietro, Filippo Glerean, Giacomo Jarc, Enrico Maria Rigoni, Shahla Y. Mathengattil, Daniele Varsano, Massimo Rontani, Andrea Perucchi, Elisa Molinari, Daniele Fausti
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-7 (2022)
Here, the authors investigate the optical response of bulk black phosphorus to mid-infrared pulses, and find that while above-gap excitation leads to a broadband light-induced transparency, sub-gap pulses drive an anomalous response, peaked at the si
Externí odkaz:
https://doaj.org/article/4eadf106d724414fad15842455310f41
Autor:
Maria Luisa Brandi, Stefania Bandinelli, Teresa Iantomasi, Francesca Giusti, Eleonora Talluri, Giovanna Sini, Fabrizio Nannipieri, Santina Battaglia, Riccardo Giusti, Colin Gerard Egan, Luigi Ferrucci
Publikováno v:
Endocrine Connections, Vol 11, Iss 3, Pp 1-11 (2022)
Objective: This study aimed to evaluate the association between the endocrine-disrupting chemical, bisphenol A (BPA) on circulating levels of 25-hydroxy vitamin D (25(OD)D) and other vitamin D metabolites in an elderly population in Italy. Methods: T
Externí odkaz:
https://doaj.org/article/4394ec5c43e54cb48e874399b6fabff4
Autor:
Francesca Miglietta, Luca Iamartino, Gaia Palmini, Francesca Giusti, Francesca Marini, Teresa Iantomasi, Maria Luisa Brandi
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2023)
Hematopoietic stem cell transplantation (HSCT) is an established therapeutic strategy for the treatment of malignant (leukemia and lymphoma) and non-malignant (thalassemia, anemia, and immunodeficiency) hematopoietic diseases. Thanks to the improveme
Externí odkaz:
https://doaj.org/article/81adbd558d8d4cd4af1394002b98193b
Autor:
Simone Donati, Francesca Marini, Francesca Giusti, Gaia Palmini, Cinzia Aurilia, Irene Falsetti, Teresa Iantomasi, Maria Luisa Brandi
Publikováno v:
Pharmaceuticals, Vol 16, Iss 5, p 637 (2023)
Vitamin D deficiency is a constantly growing health problem worldwide. Adults affected with hypovitaminosis D could experience negative consequences on their musculoskeletal system and extra-skeletal health. In fact, an optimal vitamin D status is es
Externí odkaz:
https://doaj.org/article/3c32d9cbf35245bc99efe75997f2c8ac
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
Akademický článek
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Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Inherited endocrine tumors are neoplasms of endocrine cells, transmitted via autosomal dominant germinal mutations. They present in two different forms: non-syndromic (patient has a single affected endocrine organ during his/her lifetime) or
Externí odkaz:
https://doaj.org/article/112e8b53d6f341e28c28e030cc18a8d1