Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Giuliana Longo"'
Autor:
Zollino, Silvia D’Ippolito, Giuliana Longo, Daniela Orteschi, Andrea Busnelli, Nicoletta Di Simone, Eleonora Pulcinelli, Giorgia Schettini, Giovanni Scambia, Marcella
Publikováno v:
Journal of Clinical Medicine; Volume 12; Issue 12; Pages: 3898
(1) Background: The aim of our study is to evaluate whether cell-free DNA testing can overlap the genetic testing of miscarriage tissue in women with early pregnancy loss (EPL) and length of recurrent pregnancy loss (RPL); (2) Methods: We conducted a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::91f0df513cd87332bc35cd598bf600a1
Autor:
Maria Giovanna Scioli, Michela Murdocca, Paola Spitalieri, Giuseppe Novelli, Federica Sangiuolo, Giuliana Longo, Augusto Orlandi, Mario Marini
Publikováno v:
Cellular and Molecular Bioengineering
Background Mechanical unloading in microgravity is thought to induce tissue degeneration by various mechanisms, including the inhibition of regenerative stem cell differentiation. In this work, we investigate the effects of microgravity simulation on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5b6139a5f9c702e28d15eba217ab96e
http://hdl.handle.net/2108/285072
http://hdl.handle.net/2108/285072
Autor:
Valentina Ferradini, Giovanni Ruvolo, Laura Gigante, Federica Sangiuolo, Serena Luciano, Liliana Mannucci, Chiara Conte, Nunzia Piumelli, Francesco Brancati, Giuseppe Novelli, Leila B. Salehi, Giuliana Longo
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 501
Background Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder caused by mutations in the FBN1 gene, coding for fibrillin-1. All organ systems may be affected, but particularly the cardiovascular system
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfd8907d43fd7659c38d179ed4cabc21
https://pubmed.ncbi.nlm.nih.gov/31730815
https://pubmed.ncbi.nlm.nih.gov/31730815
Autor:
Paola Borgiani, Giuseppe Novelli, Raffaella Cascella, Emiliano Giardina, Mara Maccarone, Claudia Strafella, Giuliana Longo, Federica Sangiuolo
Publikováno v:
Pharmacogenomics. 17:943-951
This review will outline the current pharmacogenomics knowledge about psoriatic arthritis with a special attention to the perspectives and the challenges for its implementation in the clinical practice. To date, different drugs have been developed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55177265d5c73084259c00d5cf780da3
https://doi.org/10.2217/pgs.16.20
https://doi.org/10.2217/pgs.16.20
Autor:
Stefano Gambardella, Claudia Strafella, Giuseppe Novelli, Emiliano Giardina, Federica Sangiuolo, Paola Borgiani, Raffaella Cascella, Giuliana Longo
Publikováno v:
ELECTROPHORESIS. 37:860-864
The hypoacusia can be classified in two clinical forms: Syndromic (SHL) and Nonsyndromic (NSHL). In particular, the NSHL describes the 70-80% of hypoacusia cases and it is mainly due to genetic factors, which are causative of the deafness at the birt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d56b44e78991bec9b5e7658bbc421a0b
https://doi.org/10.1002/elps.201500346
https://doi.org/10.1002/elps.201500346
Autor:
Silvestro Mauriello, Francesco Viola, Federica Sangiuolo, Laura Manzo, Giuliana Longo, Valeria Errichiello, Valerio Caputo, Giovanni Staurenghi, Claudia Strafella, Federico Ricci, Emiliano Giardina, Paola Borgiani, Luigi Tonino Marsella, Chiara M. Eandi, Raffaella Cascella, Andrea Cusumano, Michele Ragazzo, Giuseppe Novelli, Cinzia Ciccacci, Cecilia De Felici
Publikováno v:
Oncotarget
Age-related Macular Degeneration (AMD) represents one of the most sight-threatening diseases in developed countries that substantially impacts the patients' lifestyle by compromising everyday activities, such as reading and driving. In this context,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa922f8761a1e4bf8f0ca711102f7fb
http://hdl.handle.net/2318/1753366
http://hdl.handle.net/2318/1753366
Publikováno v:
Clinical Genetics. 89:93-98
X-linked myotubular myopathy (XLMTM) is a congenital neuromuscular disorder defined by severe hypotonia, respiratory failure and histopathologic changes in muscle biopsy. The objective of this report is to inform about our experience of genetic analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10b92c72d2eb84900ca7d622664aff3f
https://doi.org/10.1111/cge.12674
https://doi.org/10.1111/cge.12674
Autor:
Paolo Gennaro, Ikenna Valentine Aboh, Cristiano Ialongo, Valentino Valentini, Valeria Mitro, Giuliana Longo
Publikováno v:
Journal of Craniofacial Surgery. 20:1052-1055
INTRODUCTION: Starting from the 1980s, with the advent of microsurgery, microvascular flaps are used for the reconstruction of wide and complex bone defects of the maxillomandibular district. Compared with conventional and implant-supported prosthese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4ffe23cb861bec2a007bb3aa6c7f197
https://doi.org/10.1097/scs.0b013e3181abb21d
https://doi.org/10.1097/scs.0b013e3181abb21d
Autor:
Ikenna Valentine Aboh, Valentino Valentini, Giorgio Iannetti, Giuliana Longo, Andrea Torroni, Paolo Gennaro
Publikováno v:
Journal of Craniofacial Surgery. 18:1359-1369
This work focuses on the use of revascularized free flaps for the reconstruction of the major defects of the mandible after the removal of advanced-stage tumors in irradiated patients. It uses three representative cases to study the problems of compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5f8b20f12366604918d725587779ac7
https://doi.org/10.1097/scs.0b013e318068fed4
https://doi.org/10.1097/scs.0b013e318068fed4
Autor:
Federica Sangiuolo, Francesca Mariani, Ermanno Puxeddu, Alessia Comandini, Giovanni Simonetti, Marco Pallante, Monica Losi, Cesare Saltini, Gabriella Pezzuto, Francesco Cavalli, Gianluigi Sergiacomi, Augusto Orlandi, Donato Di Pierro, Massimo Amicosante, A. Bisetti, Andrea Magrini, Giuliana Longo, Maurizio Zompatori, Daniela Fraboni
In idiopathic pulmonary fibrosis (IPF), lung accumulation of excessive extracellular iron and macrophage haemosiderin may suggest disordered iron homeostasis leading to recurring microscopic injury and fibrosing damage.The current study population co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c857f7dc5f9699de2573cde9d4bdd29
http://hdl.handle.net/11585/423366
http://hdl.handle.net/11585/423366