Zobrazeno 1 - 10
of 620
pro vyhledávání: '"Cancellieri, A."'
Autor:
Angelo Ianielli, Mattia Zaghi, Chiara Di Resta, Federica Banfi, Edoardo Bellini, Mirko Luoni, Luca Massimino, Rocco Piazza, Alicia Rubio, Alessandro Sessa, Anna Bagliani, Vania Broccoli, Giulia Fagnocchi, Cinzia Cancellieri, Maurizio Ferrari, Luca Mologni, Camilla Maffezzini
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-21 (2021)
Nature Communications
Nature Communications
The investigation of genetic forms of juvenile neurodegeneration could shed light on the causative mechanisms of neuronal loss. Schinzel-Giedion syndrome (SGS) is a fatal developmental syndrome caused by mutations in the SETBP1 gene, inducing the acc
Publikováno v:
Cytopathology. 33:305-311
Cytology of serous effusions is an important diagnostic tool for the diagnosis of cancer, staging, and prognosis of the patient. Herein, we retrospectively applied the International System for Reporting Serous Fluid Cytopathology (TIS) and provided t
Autor:
Malena Daich Varela, James Bellingham, Fabiana Motta, Neringa Jurkute, Jamie M Ellingford, Mathieu Quinodoz, Kathryn Oprych, Michael Niblock, Lucas Janeschitz-Kriegl, Karolina Kaminska, Francesca Cancellieri, Hendrik P N Scholl, Eva Lenassi, Elena Schiff, Hannah Knight, Graeme Black, Carlo Rivolta, Michael E Cheetham, Michel Michaelides, Omar A Mahroo, Anthony T Moore, Andrew R Webster, Gavin Arno
Publikováno v:
Human molecular genetics, vol 32, iss 4
The purpose of this paper is to identify likely pathogenic non-coding variants in inherited retinal dystrophy (IRD) genes, using genome sequencing (GS). Patients with IRD were recruited to the study and underwent comprehensive ophthalmological evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eecf9b5f20e38556985a642ed4fc37b
https://escholarship.org/uc/item/4z14k3r2
https://escholarship.org/uc/item/4z14k3r2
Autor:
Ali Ghanbari Asad, Alireza Pasdar, Andrea Superti-Furga, Neda Sepahi, Zeinab Ravesh, Francesca Cancellieri, Saman Ghalamkari, Mathieu Quinodoz, Mehrdad Piran, Virginie G. Peter, Arash Salmaninejad, Mehran Piran, Nicola Bedoni, Carlo Rivolta, Atta Ur Rehman, Majid Mojarrad
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientific Reports
Scientific Reports
Inherited retinal dystrophies (IRDs) constitute one of the most heterogeneous groups of Mendelian human disorders. Using autozygome-guided next-generation sequencing methods in 17 consanguineous pedigrees of Iranian descent with isolated or syndromic
Publikováno v:
European review for medical and pharmacological sciences. 26(19)
On March 11, 2020, the World Health Organization (WHO) has declared the novel coronavirus (COVID-19) outbreak as a global pandemic. COVID-19 pandemic has impacted health services, including immunization programs, with a consequent reduction in vaccin
Autor:
Francesca Ambrosi, Francesca Giunchi, Elisa Capizzi, Alessandra Cancellieri, Rocco Trisolini, Andrea Ardizzoni, Michelangelo Fiorentino, Costantino Ricci
Background: The PD-L1 assessment is mandatory for the selection of patients affected by advanced non-small-cell lung cancer (NSCLC) who can benefit from the PD-1/PD-L1 checkpoint inhibitors therapy. Previous studies tested PD-L1 on cytological smears
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41a70e5b8505464bdd4632561e5816be
http://hdl.handle.net/11585/886056
http://hdl.handle.net/11585/886056
Autor:
Paolo Boscolo‐Rizzo, Claire Hopkins, Anna Menini, Michele Dibattista, Emilia Cancellieri, Nicoletta Gardenal, Margherita Tofanelli, Romina Valentinotti, Jerome R. Lechien, Luigi Angelo Vaira, Giancarlo Tirelli
Olfactory dysfunction (OD) is one of the most common symptoms of acute and long-COVID-19. QualitativeOD frequently accompanies or follows quantitative olfactory loss . Limited studies to date have combinedboth qualitative and quantitative evaluation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9044c26413139f3701c2b698bc01c92b
https://hdl.handle.net/11368/3024835
https://hdl.handle.net/11368/3024835
Autor:
Marco Chiappetta, Alessandra Cancellieri, Fabrizio Cocciolillo, Carolina Sassorossi, Lucio Calandriello, Filippo Lococo
Publikováno v:
Revista Española de Medicina Nuclear e Imagen Molecular (English Edition). 41:S12-S14
Autor:
Alicia Rubio, Serena Giannelli, Vania Broccoli, Maurizio Ferrari, Chiara Fiorillo, Daniel Orellana, Ermanna Rovida, Giulia Di Lullo, Paolo Santambrogio, Anna Cozzi, Cinzia Cancellieri, Stefano Taverna, Gian Luca Forni, Maddalena Ripamonti, Sonia Levi
Publikováno v:
Stem Cell Reports, Vol 13, Iss 5, Pp 832-846 (2019)
Stem Cell Reports
Stem Cell Reports
Summary Neuroferritinopathy (NF) is a movement disorder caused by alterations in the L-ferritin gene that generate cytosolic free iron. NF is a unique pathophysiological model for determining the direct consequences of cell iron dysregulation. We est
Autor:
Giovanni Tallini, Alessandra Cancellieri, Filippo Natali, Andrea Ardizzoni, Elisa Capizzi, Rocco Trisolini, Dario de Biase, Michelangelo Fiorentino, Marco Ferrari, Daniela Paioli, Vanina Livi
Publikováno v:
The Clinical Respiratory Journal. 13:590-597
INTRODUCTION AND OBJECTIVES: Endosonography is increasingly used for the diagnosis of centrally located, bronchoscopically invisible intrapulmonary lesions, but data regarding its utility for molecular profiling are lacking. We aimed to assess the su