Zobrazeno 1 - 10
of 152
pro vyhledávání: '"Patrizia, Noris"'
Autor:
Caterina Marconi, Alessandro Pecci, Flavia Palombo, Federica Melazzini, Roberta Bottega, Elena Nardi, Valeria Bozzi, Michela Faleschini, Serena Barozzi, Tania Giangregorio, Pamela Magini, Carlo L. Balduini, Anna Savoia, Marco Seri, Patrizia Noris, Tommaso Pippucci
Publikováno v:
Haematologica, Vol 108, Iss 7 (2022)
Inherited thrombocytopenias (IT) are genetic diseases characterized by low platelet count, sometimes associated with congenital defects or a predisposition to develop additional conditions. Next-generation sequencing has substantially improved our kn
Externí odkaz:
https://doaj.org/article/1cc5ece1395d48538027f20c78325163
Autor:
Michela Faleschini, Daniele Ammeti, Nicole Papa, Caterina Alfano, Roberta Bottega, Giorgia Fontana, Valeria Capaci, Melania E. Zanchetta, Federico Pozzani, Francesca Montanari, Valeria Petroni, Paola Giordano, Patrizia Noris, Fiorina Giona, Anna Savoia
Publikováno v:
Haematologica, Vol 107, Iss 9 (2022)
Externí odkaz:
https://doaj.org/article/1cf27688dcd34699a268e120c058176e
Autor:
Roberta Bottega, Antonio Marzollo, Maddalena Marinoni, Emmanouil Athanasakis, Ilaria Persico, Anna Monica Bianco, Michela Faleschini, Erica Valencic, Daniela Simoncini, Linda Rossini, Fabio Corsolini, Martina La Bianca, Giuseppe Robustelli, Maria Gabelli, Massimo Agosti, Alessandra Biffi, Paolo Grotto, Valeria Bozzi, Patrizia Noris, Alberto B. Burlina, Adamo Pio d'Adamo, Alberto Tommasini, Flavio Faletra, Annalisa Pastore, Anna Savoia
Publikováno v:
Haematologica, Vol 107, Iss 3 (2021)
Externí odkaz:
https://doaj.org/article/35cd2665a3f64ab1a47cd248150afba4
Autor:
Michela Faleschini, Nicole Papa, Marie-Christine Morel-Kopp, Caterina Marconi, Tania Giangregorio, Federica Melazzini, Valeria Bozzi, Marco Seri, Patrizia Noris, Alessandro Pecci, Anna Savoia, Roberta Bottega
Publikováno v:
Haematologica, Vol 107, Iss 1 (2021)
GFI1B is a transcription factor essential for the regulation of erythropoiesis and megakaryopoiesis, and pathogenic variants have been associated with thrombocytopenia and bleeding. Analysing thrombocytopenic families by whole exome sequencing, we id
Externí odkaz:
https://doaj.org/article/e909f17b60f74b0da29f7c331178c087
Autor:
Francesco Paciullo, Loredana Bury, Patrizia Noris, Emanuela Falcinelli, Federica Melazzini, Sara Orsini, Carlo Zaninetti, Rezan Abdul-Kadir, Deborah Obeng-Tuudah, Paula G. Heller, Ana C. Glembotsky, Fabrizio Fabris, Jose Rivera, Maria Luisa Lozano, Nora Butta, Remi Favier, Ana Rosa Cid, Marc Fouassier, Gian Marco Podda, Cristina Santoro, Elvira Grandone, Yvonne Henskens, Paquita Nurden, Barbara Zieger, Adam Cuker, Katrien Devreese, Alberto Tosetto, Erica De Candia, Arnaud Dupuis, Koji Miyazaki, Maha Othman, Paolo Gresele
Publikováno v:
Haematologica, Vol 105, Iss 7 (2020)
Major surgery is associated with an increased risk of venous thromboembolism (VTE), thus the application of mechanical or pharmacologic prophylaxis is recommended. The incidence of VTE in patients with inherited platelet disorders (IPD) undergoing su
Externí odkaz:
https://doaj.org/article/9e9c39b698a445ad886270f6592469e4
Autor:
Carlo Zaninetti, Paolo Gresele, Antonella Bertomoro, Catherine Klersy, Erica De Candia, Dino Veneri, Serena Barozzi, Tiziana Fierro, Maria Adele Alberelli, Valeria Musella, Patrizia Noris, Fabrizio Fabris, Carlo L. Balduini, Alessandro Pecci
Publikováno v:
Haematologica, Vol 105, Iss 3 (2020)
Patients with inherited thrombocytopenias often require platelet transfusions to raise their platelet count before surgery or other invasive procedures; moreover, subjects with clinically significant spontaneous bleeding may benefit from an enduring
Externí odkaz:
https://doaj.org/article/1641fa1000414fd994ea17768ea3d004
Autor:
Francesco Rodeghiero, Ingrid Pabinger, Margaret Ragni, Rezan Abdul-Kadir, Erik Berntorp, Victor Blanchette, Imre Bodó, Alessandro Casini, Paolo Gresele, Riitta Lassila, Frank Leebeek, David Lillicrap, Diego Mezzano, Patrizia Noris, Alok Srivastava, Alberto Tosetto, Jerzy Windyga, Barbara Zieger, Mike Makris, Nigel Key
Publikováno v:
HemaSphere, Vol 3, Iss 5 (2019)
Abstract. Healthy subjects frequently report minor bleedings that are frequently ‘background noise’ of normality rather than a true disorder. Nevertheless, unexpected or unusual bleeding may be alarming. Thus, the distinction between normal and p
Externí odkaz:
https://doaj.org/article/8fd763f3e5f446ada9c3cb5453e8b445
Autor:
Fabio Corsolini, Maria Gabelli, Daniela Simoncini, Giuseppe Robustelli, Flavio Faletra, Patrizia Noris, Martina La Bianca, Ilaria Persico, Anna Savoia, Paolo Grotto, Michela Faleschini, Alberto Tommasini, Maddalena Marinoni, Emmanouil Athanasakis, Adamo Pio D'Adamo, Annalisa Pastore, Anna Monica Bianco, Alberto Burlina, Linda Rossini, Antonio Marzollo, Roberta Bottega, Alessandra Biffi, Erica Valencic, Massimo Agosti, Valeria Bozzi
Publikováno v:
Haematologica. 107:750-754
Not abstract available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88e49530b20da59b248fd7a7f542d9ce
https://doi.org/10.3324/haematol.2021.279689
https://doi.org/10.3324/haematol.2021.279689
Autor:
Sara Orsini, Patrizia Noris, Loredana Bury, Paula G. Heller, Cristina Santoro, Rezan A. Kadir, Nora C. Butta, Emanuela Falcinelli, Ana Rosa Cid, Fabrizio Fabris, Marc Fouassier, Koji Miyazaki, Maria Luisa Lozano, Pamela Zúñiga, Claire Flaujac, Gian Marco Podda, Nuria Bermejo, Remi Favier, Yvonne Henskens, Emmanuel De Maistre, Erica De Candia, Andrew D. Mumford, Gul Nihal Ozdemir, Ibrahim Eker, Paquita Nurden, Sophie Bayart, Michele P. Lambert, James Bussel, Barbara Zieger, Alberto Tosetto, Federica Melazzini, Ana C. Glembotsky, Alessandro Pecci, Marco Cattaneo, Nicole Schlegel, Paolo Gresele
Publikováno v:
Haematologica, Vol 102, Iss 7 (2017)
Excessive bleeding at surgery is a feared complication in patients with inherited platelet disorders. However, very few studies have evaluated the frequency of surgical bleeding in these hemorrhagic disorders. We performed a worldwide, multicentric,
Externí odkaz:
https://doaj.org/article/9f23998bcc1147a48f907c78d874f179
Autor:
Diego Mezzano, Paul Harrison, Andrew L. Frelinger, Andrew D. Mumford, Patrizia Noris, Marie Lordkipanidzé, Paolo Gresele
Publikováno v:
Mezzano, D, Harrison, P, Frelinger, A L, Mumford, A D, Noris, P, Lordkipanidzé, M & Gresele, P 2022, ' Expert opinion on the use of platelet secretion assay for the diagnosis of inherited platelet function disorders : Communication from the ISTH SSC Subcommittee on Platelet Physiology ', Journal of Thrombosis and Haemostasis, vol. 20, no. 9, pp. 2127-2135 . https://doi.org/10.1111/jth.15781
Assessment of platelet secretion is crucial for diagnosing suspected inherited platelet function disorders (IPFD). A previous survey of the SSC on Platelet Physiology of the ISTH and a comprehensive review highlighted that most of the platelet secret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7378cf47556ca880f5a83036f784f033
https://research-information.bris.ac.uk/en/publications/c3791d75-652f-4886-adc2-0fc6d1feb8ec
https://research-information.bris.ac.uk/en/publications/c3791d75-652f-4886-adc2-0fc6d1feb8ec
