Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Giuseppe, Spinozzi"'
Autor:
Patrizia Suppressa, Fabio Pagella, Gennaro Mariano Lenato, Eleonora Gaetani, Ilaria Serio, Maristella Salvatora Masala, Giuseppe Spinozzi, Roberta Lizzio, Elina Matti, Annalisa De Silvestri, Giulio Cesare Passali, Maria Aguglia, Claudia Crocione, Carlo Sabbà
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Abstract Background Coronavirus Disease 2019 (COVID-19) continues to have a devastating impact across the world. A number of pre-existing common clinical conditions were reported to represent risk factors for more severe COVID-19 outcomes. Hereditary
Externí odkaz:
https://doaj.org/article/aab6260aea9f41cfbd28ca2908a2e558
Autor:
Anna Sbalchiero, Yasmin Abu Hweij, Tommaso Mazza, Elisabetta Buscarini, Claudia Scotti, Fabio Pagella, Guido Manfredi, Elina Matti, Giuseppe Spinozzi, Carla Olivieri
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Background Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular disorder, affecting 1:5000 individuals worldwide. All the genes associated to the disease (ENG, ACVRL1, SMAD4, GDF2) belong to the TGF‐β/BMPs signali
Externí odkaz:
https://doaj.org/article/b2cd898aa1024bfa88a5643da360d082
Autor:
Silvia Grignaschi, Anna Sbalchiero, Giuseppe Spinozzi, Bianca Lucia Palermo, Claudia Cantarini, Chantal Nardiello, Lorenzo Cavagna, Carla Olivieri
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
BackgroundSystemic Sclerosis (SSc) is a rare autoimmune disease whose pathogenesis is still poorly understood. The Transforming Growth Factor β superfamily is considered pivotal and a crucial role has been suggested for the type III receptor, Endogl
Externí odkaz:
https://doaj.org/article/ad2c6a68f6604cb0a210cbc3fd67a722
Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
Autor:
Fabio Pagella, Alessandro Pusateri, Eugenia Maiorano, Giuseppe Spinozzi, Sara Ugolini, Roberta Lizzio, Rosolino Mirabella, Carmine Tinelli, Carla Olivieri, Elina Matti
Publikováno v:
Acta Otorhinolaryngologica Italica, Vol 41, Iss 1, Pp 59-68 (2021)
Externí odkaz:
https://doaj.org/article/a3a031b7d3ad462e88877fdaa8b0be26
Autor:
Elina Matti, Eugenia Maiorano, Bogdan Nacu, Andrea Luceri, Fabio Sovardi, Vera Siragusa, Anna Ferrauto, Giuseppe Spinozzi, Carla Olivieri, Marco Benazzo, Fabio Pagella
Publikováno v:
Acta Otorhinolaryngologica Italica. 43:S28-S33
Autor:
Fabio Pagella, Roberta Lizzio, Sara Ugolini, Giuseppe Spinozzi, Eugenia Maiorano, Patrizia Suppressa, Carlo Sabbà, Elina Matti
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-3 (2020)
Abstract On March 11, 2020, WHO has defined the novel coronavirus disease SARS-CoV-2 (COVID-19) outbreak as a pandemic that still today continues to affect much of the world. Among the reasons for the rapid spread of SARS-CoV-2 infection, there is th
Externí odkaz:
https://doaj.org/article/3e9338c84de04155b6c1fb160b5a753b
Autor:
Patrizia Suppressa, Eugenia Maiorano, Eleonora Gaetani, Elina Matti, Gennaro Mariano Lenato, Ilaria Serio, Maristella Salvatora Masala, Giulio Cesare Passali, Maria Aguglia, Claudia Crocione, Pietro Luigi Lopalco, Francesca Caneschi, Valeria Musella, Annalisa De Silvestri, Giulia Gambini, Giuseppe Spinozzi, Carlo Sabbà, Fabio Pagella
Publikováno v:
Internal and Emergency Medicine.
Rare Disease patients manifested high concern regarding the possible increased risk of severe outcomes and worsening of disease-specific clinical manifestation due to the impact of COVID-19. Our aim was to assess the prevalence, outcomes, and impact
Autor:
Alessandra Greco, Sara Plumitallo, Laura Scelsi, Giannantonio Maggi, Matteo Sobrero, Annalisa Turco, Claudia Raineri, Natalia Arseni, Donata Cappelletti, Luigi Oltrona Visconti, Fabio Pagella, Giuseppe Spinozzi, Stefano Ghio, Carla Olivieri, Cesare Danesino
Publikováno v:
Pulmonary Circulation, Vol 8 (2018)
Hereditary hemorrhagic telangiectasia (HTT) is an autosomal dominant disease, most frequently caused by a mutation in either ENG or ACVRL1 , which can be associated with pulmonary arterial hypertension (PAH). In this report, we describe a new unpubli
Externí odkaz:
https://doaj.org/article/99d79f11771c4ea094da01286722e0f6
Autor:
Elina Matti, Gennaro M. Lenato, Fabio Pagella, Ilaria Serio, Claudia Crocione, Giuseppe Spinozzi, Eleonora Gaetani, Annalisa De Silvestri, Maristella Salvatora Masala, Maria Aguglia, Giulio Cesare Passali, Patrizia Suppressa, Carlo Sabbà, Roberta Lizzio
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Coronavirus Disease 2019 (COVID-19) continues to have a devastating impact across the world. A number of pre-existing common clinical conditions were reported to represent risk factors for more severe COVID-19 outcomes. Hereditary Hemorrha
Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
Autor:
Elina Matti, Rosolino Mirabella, Giuseppe Spinozzi, Alessandro Pusateri, Sara Ugolini, Carmine Tinelli, Carla Olivieri, Fabio Pagella, Roberta Lizzio, Eugenia Maiorano
Publikováno v:
Acta Otorhinolaryngologica Italica
Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease characterised by epistaxis. Surgical procedures for epistaxis vary from diathermocoagulation to nasal closure. The aim of this paper is to report our experience in endo