Výsledky vyhledávání - Francesco Fortunato
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1
Efficacy of rehabilitative techniques in reducing hemiplegic shoulder pain in stroke: Systematic review and meta-analysis Autor Alessandro de Sire, Lucrezia Moggio, Andrea Demeco, Francesco Fortunato, Riccardo Spanò, Vincenzo Aiello, Nicola Marotta, Antonio Ammendolia
Vydáno 2021Revisão -
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Pain Management and Rehabilitation for Central Sensitization in Temporomandibular Disorders: A Comprehensive Review Autor Martina Ferrillo, Amerigo Giudice, Nicola Marotta, Francesco Fortunato, Daniela Di Venere, Antonio Ammendolia, Pietro Fiore, Alessandro de Sire
Vydáno 2022Revisão -
4
Platelet mitochondrial dysfunction in critically ill patients: comparison between sepsis and cardiogenic shock Autor Alessandro Protti, Francesco Fortunato, Andrea Artoni, Anna Lecchi, Giovanna Motta, Giovanni Mistraletti, Cristina Novembrino, Giacomo P. Comi, Luciano Gattinoni
Vydáno 2015Artigo -
5
Exosomes from Human Periapical Cyst-MSCs: Theranostic Application in Parkinson's Disease Autor Marco Tatullo, Benedetta Marrelli, Maria Josephine Zullo, Bruna Codispoti, Francesco Paduano, Caterina Benincasa, Francesco Fortunato, Salvatore Scacco, Barbara Zavan, Tiziana Cocco
Vydáno 2020Revisão -
6
Efficacy of Virtual Reality and Exergaming in Improving Balance in Patients With Multiple Sclerosis: A Systematic Review and Meta-Analysis Autor Dario Calafiore, Marco Invernizzi, Antonio Ammendolia, Nicola Marotta, Francesco Fortunato, Teresa Paolucci, Francesco Ferraro, Claudio Curci, Agnieszka Ćwirlej-Sozańska, Alessandro de Sire
Vydáno 2021Revisão -
7
Circulating microRNAs as Potential Novel Diagnostic Biomarkers to Predict Drug Resistance in Temporal Lobe Epilepsy: A Pilot Study Autor Selene De Benedittis, Francesco Fortunato, Claudia Cava, Francesca Gallivanone, Enrico Iaccino, Maria Eugenia Caligiuri, Isabella Castiglioni, Gloria Bertoli, Ida Manna, Angelo Labate, Antonio Gambardella
Vydáno 2021Artigo -
8
A New Mitochondrial DNA Mutation in ND3 Gene Causing Severe Leigh Syndrome with Early Lethality Autor Marco Crimi, Alexandros Papadimitriou, Sara Galbiati, Phani Palamidou, Francesco Fortunato, Andreina Bordoni, Urania Papandreou, Dimitra Papadimitriou, George Hadjigeorgiou, Eurydiki Drogari, Nereo Bresolin, Giacomo P. Comi
Vydáno 2004Artigo -
9
Neural stem cells LewisX + CXCR4 + modify disease progression in an amyotrophic lateral sclerosis model Autor Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, Roberto Del Bo, Monica Nizzardo, Martina Nardini, Chiara Donadoni, Sabrina Salani, Francesco Fortunato, Sandra Strazzer, Nereo Bresolin, Giacomo P. Comi
Vydáno 2007Artigo -
10
Metformin overdose causes platelet mitochondrial dysfunction in humans Autor Alessandro Protti, Anna Lecchi, Francesco Fortunato, Andrea Artoni, N. Greppi, Sarah Vecchio, Gigliola Fagiolari, Maurizio Moggio, Giacomo P. Comi, Giovanni Mistraletti, Barbara Lanticina, Loredana Faraldi, Luciano Gattinoni
Vydáno 2012Artigo -
11
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1 Autor Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, Chiara Donadoni, Roberto Del Bo, Marco Crimi, Andreina Bordoni, Francesco Fortunato, Sandra Strazzer, Giorgia Menozzi, Sabrina Salani, Nereo Bresolin, Giacomo P. Comi
Vydáno 2005Artigo -
12
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neurons Autor Federica Rizzo, Dario Ronchi, Sabrina Salani, Monica Nizzardo, Francesco Fortunato, Andreina Bordoni, Giulia Stuppia, Roberto Del Bo, Daniela Piga, Romana Fato, Nereo Bresolin, Giacomo P. Comi, Stefania Corti
Vydáno 2016Artigo -
13
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanisms Autor Monica Nizzardo, Martina Nardini, Dario Ronchi, Sabrina Salani, Chiara Donadoni, Francesco Fortunato, Giorgia Colciago, Marianna Falcone, Chiara Simone, Giulietta Riboldi, Alessandra Govoni, Nereo Bresolin, Giacomo P. Comi, Stefania Corti
Vydáno 2011Artigo -
14
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies Autor Rachele Cagliani, Francesca Magri, Antonio Toscano, Luciano Merlini, Francesco Fortunato, C. Lamperti, Carmelo Rodolico, A. Prelle, Manuela Sironi, M. Aguennouz, Patrizia Ciscato, Antonino Uncini, Maurizio Moggio, Nereo Bresolin, Giacomo P. Comi
Vydáno 2005Artigo -
15
<scp><i>PAK3</i></scp> pathogenic variant associated with sleep‐related hypermotor epilepsy in a family with parental mosaicism Autor Antonio Gambardella, Y. C. Liu, Mark F. Bennett, Timothy E. Green, John A. Damiano, Francesco Fortunato, Matthew Coleman, Jacqueline Cherfils, Jean‐Vianney Barnier, Jozef Gécz, Melanie Bahlo, Samuel F. Berkovic, Michael S. Hildebrand
Vydáno 2025Artigo -
16
Exploring the Effectiveness of Adjunctive Cenobamate in Focal Epilepsy: A Time-Based Analysis Autor Roberta Roberti, Gianfranco Di Gennaro, Vittoria Cianci, Alfredo D’Aniello, Carlo Di Bonaventura, Giancarlo Di Gennaro, Francesco Fortunato, Edoardo Fronzoni, Alessandra Morano, Angelo Pascarella, Eleonora Rosati, Ilaria Sammarra, Emilio Russo, Simona Lattanzi
Vydáno 2025Artigo -
17
Mitochondrial Respiratory Chain Dysfunction in Muscle From Patients With Amyotrophic Lateral Sclerosis Autor V. Crugnola, C. Lamperti, Valeria Lucchini, Dario Ronchi, Lorenzo Peverelli, A. Prelle, Monica Sciacco, Andreina Bordoni, Elisa Fassone, Francesco Fortunato, Stefania Corti, Vincenzo Silani, Nereo Bresolin, Salvatore Di Mauro, Giacomo P. Comi, Maurizio Moggio
Vydáno 2010Artigo -
18
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy Autor Stefania Corti, Monica Nizzardo, Martina Nardini, Chiara Donadoni, Sabrina Salani, Dario Ronchi, Francesca Saladino, Andreina Bordoni, Francesco Fortunato, Roberto Del Bo, Dimitra Papadimitriou, Federica Locatelli, Giorgia Menozzi, Sandra Strazzer, Nereo Bresolin, Giacomo P. Comi
Vydáno 2008Artigo -
19
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients Autor Francesca Magri, Roberto Del Bo, Maria Grazia D’Angelo, Monica Sciacco, S. Gandossini, Alessandra Govoni, Laura Napoli, Patrizia Ciscato, Francesco Fortunato, Erika Brighina, Sara Bonato, Andreina Bordoni, Valeria Lucchini, Stefania Corti, Maurizio Moggio, Nereo Bresolin, Giacomo P. Comi
Vydáno 2012Artigo -
20
The Mitochondrial Disulfide Relay System Protein GFER Is Mutated in Autosomal-Recessive Myopathy with Cataract and Combined Respiratory-Chain Deficiency Autor Alessio Di Fonzo, Dario Ronchi, Tiziana Lodi, Elisa Fassone, Marco Tigano, C. Lamperti, Stefania Corti, Andreina Bordoni, Francesco Fortunato, Monica Nizzardo, Laura Napoli, Chiara Donadoni, Sabrina Salani, Francesca Saladino, Maurizio Moggio, Nereo Bresolin, Iliana Ferrero, Giacomo P. Comi
Vydáno 2009Artigo
Vyhledávací nástroje:
Související témata
Medicine
Biology
Internal medicine
Genetics
Pathology
Gene
Epilepsy
Neuroscience
Cell biology
Disease
Psychiatry
Endocrinology
Mitochondrion
Psychology
Mutation
Atrophy
Biochemistry
Bioinformatics
Mitochondrial DNA
Mitochondrial respiratory chain
Respiratory chain
Temporal lobe
Adjunctive treatment
Anatomy
Biopsy
Cohort
Combinatorics
Context (archaeology)
Cytochrome c oxidase
Dysferlin