Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Kalliopi Marinou"'
Autor:
Francesca Trojsi, Mattia Siciliano, Cinzia Femiano, Gabriella Santangelo, Christian Lunetta, Andrea Calvo, Cristina Moglia, Kalliopi Marinou, Nicola Ticozzi, Christian Ferro, Carlo Scialò, Gianni Sorarù, Amelia Conte, Yuri M. Falzone, Rosanna Tortelli, Massimo Russo, Valeria Ada Sansone, Adriano Chiò, Gabriele Mora, Vincenzo Silani, Paolo Volanti, Claudia Caponnetto, Giorgia Querin, Mario Sabatelli, Nilo Riva, Giancarlo Logroscino, Sonia Messina, Antonio Fasano, Maria Rosaria Monsurrò, Gioacchino Tedeschi, Jessica Mandrioli
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
We investigated whether the C9orf72 repeat expansion is associated with specific clinical features, comorbidities, and prognosis in patients with amyotrophic lateral sclerosis (ALS). A cohort of 1417 ALS patients, diagnosed between January 1, 2009 an
Externí odkaz:
https://doaj.org/article/187eb7f439f54cc7a5f8a7fe0c6dd03f
Autor:
Giovanni Nardo, Silvia Pozzi, Mauro Pignataro, Eliana Lauranzano, Giorgia Spano, Silvia Garbelli, Stefania Mantovani, Kalliopi Marinou, Laura Papetti, Marta Monteforte, Valter Torri, Luca Paris, Gianfranco Bazzoni, Christian Lunetta, Massimo Corbo, Gabriele Mora, Caterina Bendotti, Valentina Bonetto
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e25545 (2011)
Amyotrophic lateral sclerosis (ALS) is a fatal progressive motor neuron disease, for which there are still no diagnostic/prognostic test and therapy. Specific molecular biomarkers are urgently needed to facilitate clinical studies and speed up the de
Externí odkaz:
https://doaj.org/article/367560ff1626484aba0223c0cd7247b0
Autor:
Edoardo Nicolò Aiello, Debora Pain, Alice Radici, Riccardo Sideri, Kalliopi Marinou Aktipi, Gabriele Mora, Claudio Luzzatti
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 23:630-633
Verb-naming tests were proposed for detecting cognitive impairment in ALS, although statistical evidence on their clinical usefulness is still lacking. A total of 29 ALS patients and 29 demographic-matched healthy controls (HCs) were administered the
Akademický článek
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Autor:
Edoardo Nicolò Aiello, Debora Pain, Alice Radici, Kalliopi Marinou Aktipi, Riccardo Sideri, Ildebrando Appollonio, Gabriele Mora
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 43(9)
Background Amyotrophic lateral sclerosis (ALS) is phenotypically heterogeneous in motor manifestations, and the extent of upper vs. lower motor neuron involvement is a widespread descriptor. This study aimed to examine cognition across different ALS
Autor:
Laura Adelaide Dalla Vecchia, Emanuele Vaini, Kalliopi Marinou, Vlasta Bari, Gabriele Mora, Riccardo Sideri, Alberto Porta, Beatrice Cairo, Beatrice De Maria
Publikováno v:
CinC
In the recent years we have witnessed an increasing interest in studying cardiac control in amyotrophic lateral sclerosis (ALS) patients. The variability of the overall duration of cardiac electrical activity comprising depolarization and repolarizat
Autor:
Gianni Sorarù, Mario Sabatelli, Yuri Matteo Falzone, Raffaella Fazio, Francesca Trojsi, Federica Agosta, Gioacchino Tedeschi, Cristina Moglia, Giancarlo Logroscino, Valeria Sansone, Claudia Caponnetto, Kalliopi Marinou, Paolo Volanti, Massimo Filippi, Nilo Riva, Jessica Mandrioli, Giulia Ceccardi, Christian Lunetta, Andrea Calvo, Paride Schito, Angelo Quattrini, Laura Pozzi, Paola Carrera, Amelia Conte, Nicola Ticozzi, Massimo Russo, Rosanna Tortelli, Teuta Domi, Elisabetta Zucchi, Adriano Chiò, Carlo Scialò, Gabriele Mora, Vincenzo Silani, Giorgia Querin, Sonia Messina
Motor neuron disease (MND) is a heterogeneous group of neurodegenerative disorders defined by a progressive upper motor neuron (UMN) and lower motor neuron (LMN) loss in a varying combination, encompassing a heterogeneous clinical spectrum depending
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30d15620b4a1aa5eac570c9281bfa1b6
http://hdl.handle.net/2318/1759921
http://hdl.handle.net/2318/1759921
Autor:
Raffaello Furlan, Laura Adelaide Dalla Vecchia, Beatrice De Maria, Franca Barbic, Karsten Heusser, Beatrice Cairo, Vlasta Bari, Alberto Porta, Emanuele Vaini, Jens Jordan, Jens Tank, Kalliopi Marinou
BACKGROUND: The sympathetic baroreflex (sBR) adjusts muscle sympathetic nerve activity (MSNA) in response to arterial pressure changes but the relevance of assessing sBR control complexity is unclear. OBJECTIVE: We propose a method for the evaluation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c820631e0458b85ba9d245766be907e9
https://doi.org/10.1088/1361-6579/ab0d4b
https://doi.org/10.1088/1361-6579/ab0d4b
Autor:
Francesca, Trojsi, Mattia, Siciliano, Cinzia, Femiano, Gabriella, Santangelo, Christian, Lunetta, Andrea, Calvo, Cristina, Moglia, Kalliopi, Marinou, Nicola, Ticozzi, Christian, Ferro, Carlo, Scialò, Gianni, Sorarù, Amelia, Conte, Yuri M, Falzone, Rosanna, Tortelli, Massimo, Russo, Valeria Ada, Sansone, Adriano, Chiò, Gabriele, Mora, Vincenzo, Silani, Paolo, Volanti, Claudia, Caponnetto, Giorgia, Querin, Mario, Sabatelli, Nilo, Riva, Giancarlo, Logroscino, Sonia, Messina, Antonio, Fasano, Maria Rosaria, Monsurrò, Gioacchino, Tedeschi, Jessica, Mandrioli
Publikováno v:
Frontiers in Neuroscience
We investigated whether the C9orf72 repeat expansion is associated with specific clinical features, comorbidities, and prognosis in patients with amyotrophic lateral sclerosis (ALS). A cohort of 1417 ALS patients, diagnosed between January 1, 2009 an
Autor:
Valeria A. Sansone, Filippo Martinelli-Boneschi, Kalliopi Marinou, Yuri Falzone, Andrea Calvo, Giancarlo Comi, Giorgia Querin, Letizia Leocani, Federica Cerri, Daniele Martinelli, Gianni Sorarù, Laura Pozzi, Angelo Quattrini, Christian Lunetta, Mauro Comola, Nilo Riva, Elisabetta Pieri, Ottavia Eleonora Ferraro, Eleonora Maestri, Paolo Rossi, Raffaella Fazio, Fabio Formaglio, Ignazio Diego Lopez, Adriano Chiò, Gabriele Mora, Yuri Matteo Falzone, Marta Clerici
Summary Background Spasticity is a major determinant of disability and decline in quality of life in patients with motor neuron disease. Cannabinoids have been approved for symptomatic treatment of spasticity in multiple sclerosis. We investigated wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2be519b95dd8d6b7db7051bcf34f0eb4
http://hdl.handle.net/2318/1720174
http://hdl.handle.net/2318/1720174