Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Alessandro, Raso"'
Autor:
Manlio Mencoboni, Vincenzo Fontana, Azzurra Damiani, Antonino Spitaleri, Alessandro Raso, Luigi Carlo Bottaro, Giovanni Rossi, Luciano Canobbio, Antonella La Camera, Rosa Angela Filiberti, Paola Taveggia, Alessia Cavo
Publikováno v:
Current Oncology, Vol 29, Iss 5, Pp 3364-3374 (2022)
Background: Information on immune responses in cancer patients following mRNA COVID-19 vaccines is still insufficient, but generally, patients had impaired serological responses, especially those with hematological malignancies. We evaluated serologi
Externí odkaz:
https://doaj.org/article/828bcbf00b184cf1b83c4ebf6b9b8e72
Autor:
Morgane Morabito, Magalie Larcher, Florence MG Cavalli, Chloé Foray, Antoine Forget, Liliana Mirabal‐Ortega, Mamy Andrianteranagna, Sabine Druillennec, Alexandra Garancher, Julien Masliah‐Planchon, Sophie Leboucher, Abel Debalkew, Alessandro Raso, Olivier Delattre, Stéphanie Puget, François Doz, Michael D Taylor, Olivier Ayrault, Franck Bourdeaut, Alain Eychène, Celio Pouponnot
Publikováno v:
EMBO Molecular Medicine, Vol 11, Iss 8, Pp 1-17 (2019)
Abstract Medulloblastoma (MB) is a pediatric tumor of the cerebellum divided into four groups. Group 3 is of bad prognosis and remains poorly characterized. While the current treatment involving surgery, radiotherapy, and chemotherapy often fails, no
Externí odkaz:
https://doaj.org/article/953a146597434510bae487e93455a269
Autor:
Corrado Occella, Dario Bleidl, Paolo Nozza, Samantha Mascelli, Alessandro Raso, Giorgio Gimelli, Stefania Gimelli, Elisa Tassano
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e61311 (2013)
Porokeratosis is a rare disease of epidermal keratinization characterized by the histopathological feature of the cornoid lamella, a column of tightly fitted parakeratocytic cells, whose etiology is still unclear. Porokeratosis of Mibelli is a subtyp
Externí odkaz:
https://doaj.org/article/c49bcd6045094c9fa5bc2553c1e078ef
Autor:
Armando Cama, Elisabetta Ugolotti, Samantha Mascelli, Valeria Capra, Eddi Di Marco, Alessandro Raso, Marco Pavanello, Elisa Merello, Patrizia De Marco, Roberto Biassoni, Paolo Nozza
Publikováno v:
Journal of Neurosurgical Sciences. 64
Background Moyamoya disease (MMD) is a chronic, occlusive cerebrovascular disease characterized by bilateral steno-occlusive changes at the terminal portion of the internal carotid arteries and an abnormal vascular network at the base of the brain de
Autor:
Simona Lionti, Valeria Barresi, Felice Esposito, Filippo Flavio Angileri, Salvatore Cannavò, Alessandro Raso
Publikováno v:
Neuropathology. 38:260-267
Atypical teratoid rhabdoid tumor (ATRT) is an aggressive tumor of the CNS and characteristically occurs in the pediatric age. In adulthood, ATRT is rare and it is mainly localized in the cerebral hemispheres. Only 16 cases of ATRT have been described
Autor:
Domenico Tortora, Claudia Milanaccio, Claudia da Costa Leite, Maria Luisa Garrè, Andrea Rossi, Giovanni Morana, César Augusto Pinheiro Ferreira Alves, Gabriella D'Apolito, Mariasavina Severino, Alessandro Raso, Paolo Nozza, Armando Cama, Marcello Ravegnani
Publikováno v:
Oncotarget
// Giovanni Morana 1, * , Cesar Augusto Alves 1, 2, * , Domenico Tortora 1 , Mariasavina Severino 1 , Paolo Nozza 3 , Armando Cama 4 , Marcello Ravegnani 4 , Gabriella D’Apolito 5 , Alessandro Raso 4 , Claudia Milanaccio 6 , Claudia da Costa Leite
Autor:
Alessandro, Raso, Roberto, Biassoni
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2065
Quantitative polymerase chain reaction (PCR) is the basis of a variety of scientific applications and publications in a broad range of interests. It also plays a fundamental role in nucleic acid sequencing applications, including Next Generation Sequ
Autor:
Alessandro Raso, Roberto Biassoni
Publikováno v:
Methods in Molecular Biology ISBN: 9781493998326
Quantitative polymerase chain reaction (PCR) is the basis of a variety of scientific applications and publications in a broad range of interests. It also plays a fundamental role in nucleic acid sequencing applications, including Next Generation Sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e205a7a0a714bdc6fd5c3ec282320ede
https://doi.org/10.1007/978-1-4939-9833-3_1
https://doi.org/10.1007/978-1-4939-9833-3_1
Autor:
Alessandro Raso, Alain Eychène, Antoine Forget, Michael D. Taylor, Morgane Morabito, Magalie Larcher, Franck Bourdeaut, Florence M.G. Cavalli, Liliana Mirabal-Ortega, Olivier Delattre, Chloe Foray, Abel Debalkew, François Doz, Julien Masliah-Planchon, Sophie Leboucher, Celio Pouponnot, Alexandra Garancher, Mamy Andrianteranagna, Stéphanie Puget, Sabine Druillennec, Olivier Ayrault
Publikováno v:
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 11, Iss 8, Pp n/a-n/a (2019)
EMBO Molecular Medicine, Wiley Open Access, 2019, 6, pp.e9830. ⟨10.15252/emmm.201809830⟩
EMBO Molecular Medicine, Vol 11, Iss 8, Pp n/a-n/a (2019)
EMBO Molecular Medicine, Wiley Open Access, 2019, 6, pp.e9830. ⟨10.15252/emmm.201809830⟩
International audience; Medulloblastoma (MB) is a pediatric tumor of the cerebellum divided into four groups. Group 3 is of bad prognosis and remains poorly characterized. While the current treatment involving surgery, radiotherapy, and chemotherapy
Autor:
Chiara Pantaleoni, Davide Rossi Sebastiano, Gloria Bedini, Maurizio Paciaroni, Marco Pavanello, Veronica Saletti, Andrea Zini, Giuseppe Faragò, Elisa Ciceri, Daria Riva, Stefania Bianchi Marzoli, Sara Nava, Massimiliano Toscano, Peter Vajkoczy, Elisabeth Tournier Lasserve, Emilio Ciusani, Kinga G. Blecharz, Luigi Caputi, Nardo Nardocci, Maria Vittoria Calloni, Giorgio Bono, Maria Luisa De Lodovici, Vittorio Di Piero, Marina Grisoli, Cristina Sarti, Fioravanti Capone, Alessandro Pezzini, Maria Luisa Dell’ Acqua, Federica Zibordi, Eugenio Parati, Anna Bersano, Silvia Lanfranconi, Silvia Esposito, Marco Cenzato, Simona Binelli, Antonio Carolei, Danilo Toni, Paolo Prontera, Filippo Farina, Alfredo Romani, Patrizia Perrone, Alessandro Raso, Sandro Sanguigni, Maria Grazia Bruzzone, Leonardo Pantoni, Silvana Franceschetti, Vincenzo Di Lazzaro, Andrea Gioppo, Simona Sacco, Claudio Baracchini, Alessia Fratianni, Marialuisa Zedde, Paolo Ferroli, Filomena Caria, Francesco Acerbi, Valeria Capra, Valeria Caso
GENetics of mOyaMoyA (GEN-O-MA) project is a multicenter observational study implemented in Italy aimed at creating a network of centers involved in moyamoya angiopathy (MA) care and research and at collecting a large series and bio-repository of MA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f67fe53b148cb8006dd71acb3396284f
http://hdl.handle.net/11573/1225558
http://hdl.handle.net/11573/1225558