Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Matteo Marini"'
Autor:
Emauele Rubilotta, Matteo Marini, Greta Pettenuzzo, Marilena Gubbiotti, Alessandro Antonelli, Matteo Balzarro
Publikováno v:
Continence, Vol 6, Iss , Pp 100662- (2023)
Externí odkaz:
https://doaj.org/article/1d961b98bc844ca381f986c428053922
Autor:
Francesca Vedovo, Jacopo Leonardo Martini, Carmelo Morreale, Matteo Balzarro, Emanuele Rubilotta, Matteo Marini, Paolo Capogrosso, Lisa Di Blas, Carlo Trombetta
Publikováno v:
Continence, Vol 6, Iss , Pp 100680- (2023)
Externí odkaz:
https://doaj.org/article/39fe1d6095c748eeb14285c5fdb8e917
Publikováno v:
IEEE Transactions on Dependable and Secure Computing. 20:392-406
Tracing the sequence of library and system calls that a program makes is very helpful in the characterization of its interactions with the surrounding environment and ultimately of its semantics. Due to entanglements of real-world software stacks, ac
Autor:
Francesco Dondi, Roberto Gatta, Luca Camoni, Domenico Albano, Matteo Marini, Raffaele Giubbini, Francesco Bertagna, Carlo Rodella
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 21
Journal of Clinical Medicine, Vol 10, Iss 5064, p 5064 (2021)
Volume 10
Issue 21
Journal of Clinical Medicine, Vol 10, Iss 5064, p 5064 (2021)
The aim of this retrospective study was to investigate the ability of 18 fluorine-fluorodeoxyglucose positron emission tomography/CT (18F-FDG-PET/CT) metrics and radiomics features (RFs) in predicting the final diagnosis of solitary pulmonary nodules
Autor:
Carlo Cantile, Claudia Salvadori, Giuliano Tomelleri, Matteo Marini, Valeria Guglielmi, Gaetano Vattemi
Publikováno v:
Topics in companion animal medicine. 42
Muscular dystrophies in dogs and cats represent a heterogeneous group of inherited, sometimes congenital, but infrequently diagnosed, progressive neuromuscular disorders. A correct identification and characterization of canine and feline muscular dys
Publikováno v:
Annals of Behavioral Neuroscience. 1:07-13
Mitochondrial diseases (MDs) are a group of heterogeneous disorders due to impaired oxidative phosphorylation causing defective ATP production. The histopathological hallmark is the presence ofragged-red fibers (RRFs), muscle fibers with excessive mi
Autor:
Ubaldo Armato, Cristiano Chiamulera, Ilaria Pierpaola Dal Prà, Marzia Di Chio, Gaetano Vattemi, Roberto Chignola, Giuliano Tomelleri, Anna Maria Chiarini, Matteo Marini, Valeria Guglielmi
Publikováno v:
Clinical Science. 130:167-181
Mitochondrial disorders are heterogeneous multisystemic disorders due to impaired oxidative phosphorylation causing defective mitochondrial energy production. Common histological hallmarks of mitochondrial disorders are RRFs (ragged red fibres), musc
Autor:
Matteo Marini, Valeria Guglielmi, Giuliano Tomelleri, Gaetano Vattemi, Daniela Cecconi, Giulio Fracasso
Publikováno v:
Journal of neuropathology and experimental neurology. 77(11)
M-line is the narrow transverse band located in the center of the sarcomeric A-band that is mainly responsible for the stabilization of myosin thick filaments. A 27-year-old male patient with a positive medical history for ankylosing spondylitis pres
Autor:
Benoit Coulombe, Giuliano Tomelleri, Émilie Fiola Masson, Gaetano Vattemi, Manuela Malatesta, Diane Forget, Matteo Marini, Valeria Guglielmi
Publikováno v:
Histopathology. 67:859-865
Aims Myofibrillar myopathies (MFMs) are a group of inherited or sporadic neuromuscular disorders characterized morphologically by foci of myofibril dissolution, disintegration of the Z-disk and insoluble protein aggregates within the muscle fibres. T
Autor:
Paolo Manganotti, Dominika Nowis, V. Meneghini, Radoslaw Sadowski, Martina Tinelli, Giuliano Tomelleri, Manuela Malatesta, Laura Paoli, Gaetano Vattemi, Matteo Marini, Grzegorz M. Wilczynski, Valeria Guglielmi
Publikováno v:
Journal of Neuropathology & Experimental Neurology
Multiple myeloma (MM) accounts for ∼13% of all hematologic malignancies. Bortezomib treatment is effective in MM, but can be complicated with neurological side effects. We describe a patient with symptomatic MM who had a reversible metabolic myopat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::238654a1d11aaa44b16194a94f3ae8c9
http://hdl.handle.net/11368/2979339
http://hdl.handle.net/11368/2979339