Zobrazeno 1 - 10
of 210
pro vyhledávání: '"Laura, Masi"'
Autor:
Icro Meattini, Giulio Francolini, Vanessa Di Cataldo, Luca Visani, Carlotta Becherini, Erika Scoccimarro, Viola Salvestrini, Chiara Bellini, Laura Masi, Raffaela Doro, Federica Di Naro, Mauro Loi, Giulia Salvatore, Gabriele Simontacchi, Daniela Greto, Marco Bernini, Jacopo Nori, Lorenzo Orzalesi, Simonetta Bianchi, Monica Mangoni, Lorenzo Livi
Publikováno v:
Clinical and Translational Radiation Oncology, Vol 37, Iss , Pp 94-100 (2022)
Background and purpose: Preoperative partial breast irradiation (PBI) has got the advantage of treating a well-defined target. We report the results of the phase II ROCK trial (NCT03520894), enrolling early breast cancer (BC) patients treated with pr
Externí odkaz:
https://doaj.org/article/8f1bd43896684de4ba97c8b20e6dd6fb
Autor:
Gemma Marcucci, Paola Altieri, Salvatore Benvenga, Marta Bondanelli, Valentina Camozzi, Filomena Cetani, Luisella Cianferotti, Mirko Duradoni, Caterina Fossi, Ettore degli Uberti, Fausto Famà, Giovanna Mantovani, Claudio Marcocci, Laura Masi, Uberto Pagotto, Andrea Palermo, Simone Parri, Rosaria Maddalena Ruggeri, Maria Chiara Zatelli, Maria Luisa Brandi, On behalf of “Hypoparathyroidism Working Group” affiliated to the Italian Society of Endocrinology (S.I.E.)
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Abstract Background Hypoparathyroidism (HypoPT) or pseudo-hypoparathyroidism (pseudo-HypoPT) during pregnancy may cause maternal and fetal/neonatal complications. In this regard, only a few case reports or case series of pregnant or lactating women h
Externí odkaz:
https://doaj.org/article/8e962859912f412abf830c3b95403a25
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:
Muhammad Kassim Javaid, Alison Boyce, Natasha Appelman-Dijkstra, Juling Ong, Patrizia Defabianis, Amaka Offiah, Paul Arundel, Nick Shaw, Valter Dal Pos, Ann Underhil, Deanna Portero, Lisa Heral, Anne-Marie Heegaard, Laura Masi, Fergal Monsell, Robert Stanton, Pieter Durk Sander Dijkstra, Maria Luisa Brandi, Roland Chapurlat, Neveen Agnes Therese Hamdy, Michael Terrence Collins
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-17 (2019)
Abstract Fibrous Dysplasia / McCune Albright syndrome (FD/MAS) represents a wide spectrum of diseases due to somatic gain-of-function mutations of the GNAS gene. The mutation leads to overactivity in the target tissues and to a wide phenotype of clin
Externí odkaz:
https://doaj.org/article/bbcbbee103a0444987b518c3f8cf2459
Autor:
Laura Masi, Pascale Abadie, Catherine Herba, Mutsuko Emond, Marie-Pier Gingras, Leila Ben Amor
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Video game addiction in young children is relevant, but it is especially important for children with ADHD. In order to obtain more data about the use of video games by Canadian children, and in particular by ADHD children, we explored the modalities
Externí odkaz:
https://doaj.org/article/c03586db391b4ce38843be25431cd9cf
Autor:
Stefania Clemente, Laura Masi, Christian Fiandra, Elisabetta Cagni, Elena Villaggi, Marco Esposito, Francesca Romana Giglioli, Carmelo Marino, Lidia Strigari, Cristina Garibaldi, Michele Stasi, Pietro Mancosu, Serenella Russo
Publikováno v:
Physics and Imaging in Radiation Oncology, Vol 5, Iss , Pp 93-96 (2018)
Large uncertainties in output factor (OF) small fields dosimetry motivated multicentric studies. The focus of the study was the determination of the OFs, for different linacs and radiosurgery units, using new-generation detectors. Intercomparison stu
Externí odkaz:
https://doaj.org/article/cdf4bffa1df04839ab758864bbfca1ce
Autor:
Umberto Tarantino, Giovanni Iolascon, Luisella Cianferotti, Laura Masi, Gemma Marcucci, Francesca Giusti, Francesca Marini, Simone Parri, Maurizio Feola, Cecilia Rao, Eleonora Piccirilli, Emanuela Basilici Zanetti, Noemi Cittadini, Rosaria Alvaro, Antimo Moretti, Dario Calafiore, Giuseppe Toro, Francesca Gimigliano, Giuseppina Resmini, Maria Luisa Brandi
Publikováno v:
Journal of Orthopaedics and Traumatology, Vol 18, Iss S1, Pp 3-36 (2017)
Abstract Background The Italian Society for Orthopaedics and Traumatology conceived this guidance—which is primarily addressed to Italian orthopedic surgeons, but should also prove useful to other bone specialists and to general practitioners—in
Externí odkaz:
https://doaj.org/article/6c7d3896bbb44178b31b412b5f1e3e89
Autor:
Gemma Marcucci, Guglielmo Beccuti, Giulia Carosi, Filomena Cetani, Luisella Cianferotti, Anna Maria Colao, Carolina Di Somma, Mirko Duradoni, Antonia Elefante, Lucia Ghizzoni, Massimo Giusti, Andrea Gerardo Lania, Elisabetta Lavezzi, Bruno Madeo, Giovanna Mantovani, Claudio Marcocci, Laura Masi, Simone Parri, Francesca Pigliaru, Assunta Santonati, Antonio Spada, Lara Vera, Maria Luisa Brandi
Publikováno v:
Journal of Endocrinological Investigation. 45:1653-1662
Purpose The main purpose of this study was to investigate the effects of 12 months of rhPTH (1–84) (Natpar®) treatment in a cohort of patients selected according to the indications of hypoparathyroidism guidelines. The use of recombinant human PTH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1411da89995d3dbb1fc0e46099ac6cdc
https://doi.org/10.1007/s40618-022-01800-y
https://doi.org/10.1007/s40618-022-01800-y
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:
Laura Masi
Publikováno v:
International Journal of Bone Fragility. 1:114-119
Purpose: Gaucher disease (GD; OMIM # 230800) is an autosomal recessively inherited lysosomal storage disease. GD is caused by a deficiency of the lysosomal enzyme, glucocerebrosidase (GBA, also called acid ß-glucosidase or GCase), which hydrolyzes g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8897bb9ee42a845436357ba131377f8
https://doi.org/10.57582/ijbf.210103.114
https://doi.org/10.57582/ijbf.210103.114