Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gennaro Mariano Lenato"'
Autor:
Emanuela Resta, Eustachio Cuscianna, Paola Pierucci, Carlo Custodero, Vincenzo Solfrizzi, Carlo Sabbà, Chiara Maria Palmisano, Federica Barratta, Maria Luisa De Candia, Maria Grazia Tummolo, Elena Capozza, Sonia Lomuscio, Lucrezia De Michele, Silvio Tafuri, Onofrio Resta, Gennaro Mariano Lenato
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
BackgroundExertional dyspnoea in post-COVID syndrome is a debilitating manifestation, requiring appropriate comprehensive management. However, limited-resources healthcare systems might be unable to expand their healthcare-providing capacity and are
Externí odkaz:
https://doaj.org/article/6b98a95bde9e477aab27554f80041d27
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:
Valentina Scarano, Daniele De Santis, Patrizia Suppressa, Patrizia Lastella, Gennaro Mariano Lenato, Vincenzo Triggiani, Carlo Sabbà
Publikováno v:
Case Reports in Endocrinology, Vol 2013 (2013)
Externí odkaz:
https://doaj.org/article/fb6947a2be8a498bab70377012c581ad
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff8a827ac63cfa8ffc4d4aad430c9158
https://doi.org/10.1007/s11739-023-03287-8
https://doi.org/10.1007/s11739-023-03287-8
Publikováno v:
Intertexts. 26:128-139
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::991a57f4411293d10c9e3cb857fd7e35
https://doi.org/10.1353/itx.2022.0007
https://doi.org/10.1353/itx.2022.0007
Autor:
Maria Luisa Cavallo, Anna Castrovilli, Alessia D’Introno, Antonio Perrone, Alberto Polito, Gennaro Mariano Lenato, Carlo Sabbà
Publikováno v:
Journal of Medical Cases. 8:265-268
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2da3f74ca5dd7928350ddbfdeca00100
https://doi.org/10.14740/jmc2865w
https://doi.org/10.14740/jmc2865w
Autor:
Valentina, Scarano, Scarano, Valentina, Daniele, De Santis, De Santis, Daniele, Patrizia, Suppressa, Suppressa, Patrizia, Patrizia, Lastella, Lastella, Patrizia, Gennaro Mariano, Lenato, Lenato Gennaro, Mariano, Vincenzo, Triggiani, Triggiani, Vincenzo, Carlo, Sabbà, Sabbà, Carlo
Publikováno v:
Case Reports in Endocrinology
Case Reports in Endocrinology, Vol 2013 (2013)
Case Reports in Endocrinology, Vol 2013 (2013)
A 65-year-old man was referred to our clinic for the rehabilitation of right hemiparesis caused by ischaemic stroke. Hypertension, postphlebitic syndrome of lower limbs, frequent nose bleeding, and anemia were present in his history; in his adolescen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::098724fec61b43c2f1aa87272c2ad22c
http://europepmc.org/articles/PMC3638540
http://europepmc.org/articles/PMC3638540
Autor:
Paola Sala, Emanuela Lucci Cordisco, Vittoria Stigliano, Lucio Bertario, Angelo Andriulli, Alessandro Stella, Ada Piepoli, Patrizia Lastella, Cristina Host, Maria Grazia Tibiletti, Daria Carmela Loconte, Cristina Bozzao, Daniela Pierannunzio, Maurizio Ponz de Leon, Emanuele Damiano Luca Urso, Nicoletta Resta, Francesco Susca, Rosanna Bagnulo, Gennaro M. Lenato, Daniela Turchetti, Carmela Di Gregorio, Laura Giunti, Alessandra Viel, Liliana Varesco, Mara Fornasarig, Luigi Memo, Riccardo Capocaccia, Maurizio Genuardi, Paola Grammatico, Carlo Sabbà
BACKGROUND: Germline mutations in the STK11/LKB1 gene cause Peutz-Jeghers syndrome, an autosomal-dominantly inherited condition characterized by mucocutaneous pigmentation, hamartomatous gastrointestinal polyposis, and an increased risk for various m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f47598fd65d4214874439972885f755
https://hdl.handle.net/11380/1060916
https://hdl.handle.net/11380/1060916
