Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Iolanda Santimone"'
Autor:
Giovannina Rotundo, Eris Bidollari, Daniela Ferrari, Iolanda Spasari, Laura Bernardini, Federica Consoli, Alessandro De Luca, Iolanda Santimone, Giuseppe Lamorte, Simone Migliore, Ferdinando Squitieri, Angelo Luigi Vescovi, Jessica Rosati
Publikováno v:
Stem Cell Research, Vol 29, Iss , Pp 174-178 (2018)
Juvenile Onset Huntington's Disease (JOHD) is a rare variant of HD withage of onset ≤20 years, accounting for 3–10% of all HD patients. The rarity occurrence of JOHD cases, who severely progress towards mental and physical disability with atypica
Externí odkaz:
https://doaj.org/article/a3491d5ed87a4716be8fd9e6a66aa077
Autor:
Eris Bidollari, Giovannina Rotundo, Daniela Ferrari, Ornella Candido, Laura Bernardini, Federica Consoli, Alessandro De Luca, Iolanda Santimone, Giuseppe Lamorte, Andrea Ilari, Ferdinando Squitieri, Angelo Luigi Vescovi, Jessica Rosati
Publikováno v:
Stem Cell Research, Vol 28, Iss , Pp 145-148 (2018)
Huntington's disease (HD) is an incurable, autosomal dominant, hereditary neurodegenerative disorder that typically manifests itself in midlife. This pathology is linked to the deregulation of multiple, as yet unknown, cellular processes starting bef
Externí odkaz:
https://doaj.org/article/15d6bf6e86204858b1698c45729a5078
Autor:
Jessica Rosati, Eris Bidollari, Giovannina Rotundo, Daniela Ferrari, Barbara Torres, Laura Bernardini, Federica Consoli, Alessandro De Luca, Iolanda Santimone, Giuseppe Lamorte, Ferdinando Squitieri, Angelo Luigi Vescovi
Publikováno v:
Stem Cell Research, Vol 27, Iss , Pp 86-89 (2018)
Huntington Disease (HD) is an autosomal dominant disorder characterized by motor, cognitive and behavioral features caused by a CAG expansion in the HTT gene beyond 35 repeats. The juvenile form (JHD) may begin before the age of 20 years and is assoc
Externí odkaz:
https://doaj.org/article/5cc7146cdf624a4f96733c81021a34e8
Autor:
Manuel Daldin, Valentina Fodale, Cristina Cariulo, Lucia Azzollini, Margherita Verani, Paola Martufi, Maria Carolina Spiezia, Sean M. Deguire, Marta Cherubini, Douglas Macdonald, Andreas Weiss, Alberto Bresciani, Jean-Paul Gerard Vonsattel, Lara Petricca, J. Lawrence Marsh, Silvia Gines, Iolanda Santimone, Massimo Marano, Hilal A. Lashuel, Ferdinando Squitieri, Andrea Caricasole
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-15 (2017)
Abstract Conformational changes in disease-associated or mutant proteins represent a key pathological aspect of Huntington’s disease (HD) and other protein misfolding diseases. Using immunoassays and biophysical approaches, we and others have recen
Externí odkaz:
https://doaj.org/article/28a4ca589dda4cb5b33f36313fe3c9c6
Autor:
Ginevra Biino, Iolanda Santimone, Cosetta Minelli, Rossella Sorice, Bruno Frongia, Michela Traglia, Sheila Ulivi, Augusto Di Castelnuovo, Martin Gögele, Teresa Nutile, Marcella Francavilla, Cinzia Sala, Nicola Pirastu, Chiara Cerletti, Licia Iacoviello, Paolo Gasparini, Daniela Toniolo, Marina Ciullo, Peter Pramstaller, Mario Pirastu, Giovanni de Gaetano, Carlo L Balduini
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e54289 (2013)
Background and objectivesAlthough several studies demonstrated that platelet count is higher in women, decreases with age, and is influenced by genetic background, most clinical laboratories still use the reference interval 150-400×10(9) platelets/L
Externí odkaz:
https://doaj.org/article/7cfa15a8a75b41869bdad94b70cf2119
Autor:
Iolanda Santimone, Augusto Di Castelnuovo, Amalia De Curtis, Maria Spinelli, Daniela Cugino, Francesco Gianfagna, Francesco Zito, Maria Benedetta Donati, Chiara Cerletti, Giovanni de Gaetano, Licia Iacoviello
Publikováno v:
Haematologica, Vol 96, Iss 8 (2011)
Background The understanding of non-genetic regulation of platelet indices - platelet count, plateletcrit, mean platelet volume, and platelet distribution width - is limited. The association of these platelet indices with a number of biochemical, env
Externí odkaz:
https://doaj.org/article/2b35d575ebc1405fa97ebd2290b8be44
Autor:
Augusto Di Castelnuovo, Simona Costanzo, Marialaura Bonaccio, Livia Rago, Amalia De Curtis, Mariarosaria Persichillo, Francesca Bracone, Marco Olivieri, Chiara Cerletti, Maria Benedetta Donati, Giovanni de Gaetano, Licia Iacoviello, Jos Vermylen, Ignacio De Paula Carrasco, Simona Giampaoli, Antonio Spagnuolo, Deodato Assanelli, Vincenzo Centritto, Pasquale Spagnuolo, Dante Staniscia, Francesco Zito, Americo Bonanni, Roberto Lorenzet, Antonio Mascioli, Domenico Rotilio, Francesco Gianfagna, Maurizio Giacci, Antonella Padulo, Dario Petraroia, Federico Marracino, Maria Spinelli, Christian Silvestri, Francesca De Lucia, Branislav Vohnout, Franco Zito, Angelita Verna, Maura Di Lillo, Irene Di Stefano, Agostino Pannichella, Antonio Rinaldo Vizzarri, Agnieszka Pampuch, Antonella Arcari, Daniela Barbato, Carmine Di Giorgio, Sara Magnacca, Simona Panebianco, Antonello Chiovitti, Sergio Caccamo, Vanesa Caruso, Daniela Cugino, Alessandra Ferri, Concetta Castaldi, Marcella Mignogna, Tomasz Guszcz, Romina di Giuseppe, Paola Barisciano, Lorena Buonaccorsi, Floriana Centritto, Antonella Cutrone, Francesca Fanelli, Iolanda Santimone, Anna Sciarretta, Isabella Sorella, Emanuela Plescia, Alessandra Molinaro, Christiana Cavone, Giovanna Galuppo, Dolores D'Angelo, Rosanna Ramacciato, Amalia de Curtis
Publikováno v:
JACC: Heart Failure. 5:837-844
Objectives The aim of this study was to assess the hypothesis that alcohol consumption is associated with onset of atrial fibrillation (AF) and/or heart failure (HF). Background The connection between ethanol intake and AF or HF remains controversial
Autor:
Loris Belcastro, Sabrina Maffi, Simone Migliore, Maria Gabriele, Maria Giovanna Dema, Iolanda Santimone, Ferdinando Squitieri, Cristiana Borrelli, Barbara D’Alessio, Caterina Fusilli
Publikováno v:
Clinical studies.
Background LIRH Foundation started to collect data from HD subjects and families since 2001. The collection includes data from LIRH archives, REGISTRY (since 2004) and ENROLL-HD (since 2014) data. Aims To develop a large HD database starting from ENR
Autor:
George Pounis, Simona Costanzo, Marialaura Bonaccio, Augusto Di Castelnuovo, Amalia de Curtis, Emilia Ruggiero, Mariarosaria Persichillo, Chiara Cerletti, Maria Benedetta Donati, Giovanni de Gaetano, Licia Iacoviello, Jos Vermylen, Ignacio De Paula Carrasco, Simona Giampaoli, Antonio Spagnuolo, Deodato Assanelli, Vincenzo Centritto, Pasquale Spagnuolo, Dante Staniscia, Americo Bonanni, Amalia De Curtis, Roberto Lorenzet, Antonio Mascioli, Marco Olivieri, Domenico Rotilio, Francesco Gianfagna, Maurizio Giacci, Antonella Padulo, Dario Petraroia, Sara Magnacca, Federico Marracino, Maria Spinelli, Christian Silvestri, Giuseppe dell'Elba, Claudio Grippi, Francesca De Lucia, Branislav Vohnout, Angelita Verna, Maura Di Lillo, Irene Di Stefano, Agnieszka Pampuch, Agostino Pannichella, Antonio Rinaldo Vizzarri, Daniela Barbato, Francesca Bracone, Carmine Di Giorgio, Simona Panebianco, Antonello Chiovitti, Sergio Caccamo, Vanesa Caruso, Daniela Cugino, Francesco Zito, Alessandra Ferri, Concetta Castaldi, Marcella Mignogna, Tomasz Guszcz, Paola Barisciano, Lorena Buonaccorsi, Floriana Centritto, Antonella Cutrone, Francesca Fanelli, Iolanda Santimone, Anna Sciarretta, Isabella Sorella, Emanuela Plescia, Alessandra Molinaro, Christiana Cavone, Giovanna Galuppo, Dolores D'Angelo, Rosanna Ramacciato
The effect of the polyphenol content of the human diet on mortality risk is not yet fully understood. The aim of this study was to evaluate the association of a polyphenol-rich diet with mortality rate and a possible mediation effect by inflammation,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc7e7dd37c7e21cfcadfafd7fbf4f7c7
http://hdl.handle.net/11383/2078028
http://hdl.handle.net/11383/2078028
Autor:
Daniela Ferrari, Angelo L. Vescovi, Giuseppe Lamorte, Federica Consoli, Ferdinando Squitieri, Giovannina Rotundo, Simone Migliore, Laura Bernardini, Jessica Rosati, Iolanda Spasari, Iolanda Santimone, Eris Bidollari, Alessandro De Luca
Publikováno v:
Stem Cell Research, Vol 29, Iss, Pp 174-178 (2018)
Juvenile Onset Huntington's Disease (JOHD) is a rare variant of HD withage of onset ≤20 years, accounting for 3–10% of all HD patients. The rarity occurrence of JOHD cases, who severely progress towards mental and physical disability with atypica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a84c06dcf8a9a0d7ed3f629bf35c01c0
http://hdl.handle.net/11573/1340260
http://hdl.handle.net/11573/1340260