Zobrazeno 1 - 10
of 1 559
pro vyhledávání: '"Mordenti A."'
Autor:
L. Sangiorgi, M. Boarini, M. Mordenti, V. Wang, I. Westerheim, R. T. Skarberg, M. Cavaller-Bellaubi, James Clancy, R. Pinedo-Villanueva, E. J. V. Lente, M. Marchetti
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-17 (2024)
Abstract Background SATURN (Systematic Accumulation of Treatment practices and Utilisation, Real world evidence, and Natural history data) for the rare condition osteogenesis imperfecta (OI) has the objective to create a common core dataset by utilis
Externí odkaz:
https://doaj.org/article/9e0eb5f131234f7287179751990c9c7c
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-6 (2024)
Abstract Regulatory marketing authorisation is not enough to ensure patient access to new medicinal products. Health Technology Assessment bodies may require data on effectiveness, relative effectiveness, and cost-effectiveness. Healthcare systems ma
Externí odkaz:
https://doaj.org/article/9139e8b73f18409880a07a62d7fd0b25
Plasma p-tau181 and amyloid markers in Alzheimer’s disease: A comparison between Lumipulse and SIMOA
Autor:
Quaresima, Virginia, Pilotto, Andrea, Trasciatti, Chiara, Tolassi, Chiara, Parigi, Marta, Bertoli, Diego, Mordenti, Cristina, Galli, Alice, Rizzardi, Andrea, Caratozzolo, Salvatore, Benussi, Alberto, Ashton, Nicholas J., Blennow, Kaj, Zetterberg, Henrik, Giliani, Silvia, Brugnoni, Duilio, Padovani, Alessandro
Publikováno v:
In Neurobiology of Aging November 2024 143:30-40
Autor:
Maria Gnoli, Marco Gambarotti, Alberto Righi, Eric Lodewijk Staals, Andrea Evangelista, Morena Tremosini, Evelise Brizola, Marina Mordenti, Manila Boarini, Manuela Locatelli, Elena Pedrini, Luca Sangiorgi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Multiple osteochondromas is genetic disorder characterized by the formation of multiple benign cartilage-capped bone tumors, named osteochondromas, during skeletal development. The most feared complication is the secondary periphe
Externí odkaz:
https://doaj.org/article/39630631ea254982b0c1ea691e0ae7c2
Autor:
Marina Mordenti, Morena Tremosini, Manuela Locatelli, Maria Gnoli, Cristiana Forni, Elena Pedrini, Manila Boarini, Luca Sangiorgi
Publikováno v:
BMC Health Services Research, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Background Only a few studies explore the role of nurses in genetic counselling and genetic health care, and none of them is related to orphan diseases. In addition, few studies address the issue of finding variables that might affect the ec
Externí odkaz:
https://doaj.org/article/757a96f5360d46319f5d5a824e1c932e
Publikováno v:
In Estuarine, Coastal and Shelf Science April 2024 299
Autor:
Marina Mordenti, Manila Boarini, Federico Banchelli, Diego Antonioli, Serena Corsini, Maria Gnoli, Manuela Locatelli, Elena Pedrini, Eric Staals, Giovanni Trisolino, Marcella Lanza, Luca Sangiorgi
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2024)
IntroductionThe present study aims to describe a large cohort of Italian patients affected by osteogenesis imperfecta, providing a picture of the clinical bony and non-bony features and the molecular background to improve knowledge of the disease to
Externí odkaz:
https://doaj.org/article/b2a40acbb65c4dc8a66e41fd68594fc1
Autor:
Priego Zurita, Ana Luisa, Grasemann, Corinna, Boarini, Manila, Chapurlat, Roland, Mordenti, Marina, Javaid, Muhammad Kassim, Appelman-Dijkstra, Natasha M.
Publikováno v:
In European Journal of Medical Genetics December 2023 66(12)
Autor:
Elmi, Alberto, Casalini, Antonio, Bertocchi, Martina, Emmanuele, Pietro, Aniballi, Camilla, Parmeggiani, Albamaria, Govoni, Nadia, Ventrella, Domenico, Mordenti, Oliviero, Bacci, Maria Laura
Publikováno v:
In Research in Veterinary Science November 2023 164
Autor:
D'Andrea, G., Pascale, R., Vatamanu, O., Giacomini, M.E., Caroccia, N., Giannella, M., Carloni, A.L., Cesa, F., Mordenti, O., Muratori, R., Tarricone, I., Viale, P.
Publikováno v:
In Journal of Psychosomatic Research April 2023 167