Zobrazeno 1 - 10
of 238
pro vyhledávání: '"Michele D'Alto"'
Autor:
Michele D'Alto, Emanuele Romeo, Paola Argiento, Andrea Vergara, Eleonora Caiazza, Antonio Orlando, Rosa Franzese, Giancarlo Scognamiglio, Berardo Sarubbi, Konstantinos Dimopoulos
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 17, Iss , Pp 100526- (2024)
Pulmonary arterial hypertension (PAH) is defined as increase in mean pulmonary arterial pressure and pulmonary vascular resistance (PVR). It can be associated with congenital heart disease (CHD) with the following subtypes: 1) uncorrected left-to-rig
Externí odkaz:
https://doaj.org/article/a44ca906487e48079ab64e307aa9ca44
Autor:
Ioannis T. Farmakis, Amalia Baroutidou, Vasiliki Patsiou, Alexandra Arvanitaki, Ioannis Doundoulakis, Lukas Hobohm, Stefanos Zafeiropoulos, Stavros V. Konstantinides, Michele D'Alto, Roberto Badagliacca, George Giannakoulas
Publikováno v:
ERJ Open Research, Vol 10, Iss 1 (2024)
Background Pulmonary arterial hypertension (PAH)-targeted therapies exert significant haemodynamic changes; however, systematic synthesis is currently lacking. Methods We searched PubMed, CENTRAL and Web of Science for studies evaluating mean pulmona
Externí odkaz:
https://doaj.org/article/93a2b0e294a44df4af8a85255ef746b9
Autor:
Michele Correale, Francesco Chirivì, Ester Maria Lucia Bevere, Lucia Tricarico, Michele D’Alto, Roberto Badagliacca, Natale D. Brunetti, Carmine Dario Vizza, Stefano Ghio
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 8, p 2444 (2024)
Pulmonary arterial hypertension is a complex pathology whose etiology is still not completely well clarified. The pathogenesis of pulmonary arterial hypertension involves different molecular mechanisms, with endothelial dysfunction playing a central
Externí odkaz:
https://doaj.org/article/5bad76525a3e4e02b30eb0142c81d5fb
Autor:
Gaetano Rea, Marialuisa Bocchino, Roberta Lieto, Roberta Eufrasia Ledda, Michele D’Alto, Marco Sperandeo, Raffaella Lucci, Patrizio Pasquinelli, Stefano Sanduzzi Zamparelli, Giorgio Bocchini, Tullio Valente, Giacomo Sica
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 3, p 797 (2024)
Hypersensitivity pneumonitis (HP) is a diffuse parenchymal lung disease (DLPD) characterized by complex interstitial lung damage with polymorphic and protean inflammatory aspects affecting lung tissue targets including small airways, the interstitium
Externí odkaz:
https://doaj.org/article/5dcc0fc3a2584c96b9d7eb98a0f0dff1
Autor:
Paul Forfia, Raymond Benza, Michele D'Alto, Teresa De Marco, Jean M. Elwing, Robert Frantz, Francois Haddad, Ronald Oudiz, Ioana R. Preston, Stephan Rosenkranz, John Ryan, Robert Schilz, Oksana A. Shlobin, Jean‐Luc Vachiery, Carmine Dario Vizza, Anton Vonk Noordegraaf, Margaret R. Sketch, Meredith Broderick, Vallerie McLaughlin
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 2, Pp n/a-n/a (2023)
Abstract Right heart (RH) structure and function are major determinants of symptoms and prognosis in pulmonary arterial hypertension (PAH). RH imaging provides detailed information, but evidence and guidelines on the use of RH imaging in treatment de
Externí odkaz:
https://doaj.org/article/ce8abfb9f6ab4b669e83e51505d50fe2
Autor:
Pier Paolo Bassareo, Michele D’Alto
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 17, p 13227 (2023)
Pulmonary hypertension (PH) is a multifaceted illness causing clinical manifestations like dyspnea, fatigue, and cyanosis. If left untreated, it often evolves into irreversible pulmonary arterial hypertension (PAH), leading to death. Metabolomics is
Externí odkaz:
https://doaj.org/article/919dce1693ef4d17ab2397395bb3fbde
Autor:
Gaetano Rea, Nicola Sverzellati, Marialuisa Bocchino, Roberta Lieto, Gianluca Milanese, Michele D’Alto, Giorgio Bocchini, Mauro Maniscalco, Tullio Valente, Giacomo Sica
Publikováno v:
Diagnostics, Vol 13, Iss 14, p 2333 (2023)
Diffuse lung disorders (DLDs) and interstitial lung diseases (ILDs) are pathological conditions affecting the lung parenchyma and interstitial network. There are approximately 200 different entities within this category. Radiologists play an increasi
Externí odkaz:
https://doaj.org/article/29a3b73693ea46a0874bfc3875113284
Autor:
Roberto Badagliacca, Michele D'Alto, Stefano Ghio, Paola Argiento, Natale Daniele Brunetti, Gavino Casu, Nadia Cedrone, Marco Confalonieri, Marco Corda, Michele Correale, Carlo D'Agostino, Lucrezia De Michele, Serena Di Marino, Domenico Filomena, Giuseppe Galgano, Alessandra Greco, Carlo Lombardi, Giovanna Manzi, Valentina Mercurio, Massimiliano Mulè, Giuseppe Paciocco, Silvia Papa, Emanuele Romeo, Laura Scelsi, Davide Stolfo, Patrizio Vitulo, Carmine Dario Vizza
Publikováno v:
ERJ Open Research, Vol 8, Iss 4 (2022)
Rationale Demographic characteristics of pulmonary arterial hypertension (PAH) patients have changed over time, but the effects of cardiovascular risk factors on risk status and pulmonary vascular resistance (PVR) reduction with initial oral combinat
Externí odkaz:
https://doaj.org/article/ca54f9de6663460694a59bdbd46c1325
Autor:
Pier Paolo Bassareo, Paola Argiento, Colin Joseph McMahon, Esme Dunne, Kevin Patrick Walsh, Maria Giovanna Russo, Michele D’Alto
Publikováno v:
Children, Vol 10, Iss 3, p 518 (2023)
Introduction: Paediatric pulmonary hypertension (PH) represents a heterogeneous illness that is responsible for high morbidity and mortality if left without treatment. Idiopathic pulmonary arterial hypertension (IPAH) is a subtype of PAH rarely seen
Externí odkaz:
https://doaj.org/article/15699de147574935be48bde796824133
Autor:
Laurent Godinas, Keerthana Iyer, Gergely Meszaros, Rozenn Quarck, Pilar Escribano-Subias, Anton Vonk Noordegraaf, Pavel Jansa, Michele D’Alto, Milan Luknar, Senka Milutinov Ilic, Catharina Belge, Olivier Sitbon, Abílio Reis, Stephan Rosenkranz, Joanna Pepke-Zaba, Marc Humbert, Marion Delcroix
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background During the COVID-19 pandemic, most of the health care systems suspended their non-urgent activities. This included the cancellation of consultations for patients with rare diseases, such as severe pulmonary hypertension (PH), resu
Externí odkaz:
https://doaj.org/article/e7151f016f564639a30ce8eab06920d0