Zobrazeno 1 - 10
of 237
pro vyhledávání: '"Andrea, Zanichelli"'
Autor:
Antonio Gidaro, Leyla La Cava, Mattia Donadoni, Valentina Popescu Janu, Chiara Cogliati, Antonio Luca Brucato, Andrea Zanichelli, Mauro Cancian, Emanuele Bizzi
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionCardiovascular pathologies represent the first cause of death in uremic patients and are among the leading causes of mortality in patients with hereditary angioedema due to C1-inhibitor deficiency (HAE-C1INH). Before 2020, the most common
Externí odkaz:
https://doaj.org/article/e4294dd02fb542d38f1ada3f2ad89949
Autor:
Camilla Ronchei, Luciana Mantovani, Daniela Scorza, Andrea Zanichelli, Andrea Bernasconi, Giacomo Magnani, Daniele Pontiroli, Michele Sidoli, Sabrina Vantadori
Publikováno v:
Composites Part C: Open Access, Vol 14, Iss , Pp 100494- (2024)
The present paper is focused to understand the reinforcement mechanisms exerted by GO nanosheets to both strengthen and toughen cement-matrix composites since, despite intensive research, such mechanisms are still not completely clear. To such an aim
Externí odkaz:
https://doaj.org/article/a3431bfe98cd4ace9137c975691751a6
Autor:
Daniela Scorza, Andrea Carpinteri, Camilla Ronchei, Andrea Zanichelli, Sabrina Vantadori, Raimondo Luciano
Publikováno v:
Frattura ed Integrità Strutturale, Vol 18, Iss 67, Pp 280-291 (2024)
In the present paper, the mechanical behaviour of edge-cracked nanobeams under Mixed-Mode loading is analytically investigated by means of the Stress-Driven nonlocal model. Firstly, the proposed formulation is outlined, and then applied to the case o
Externí odkaz:
https://doaj.org/article/830745756c8e40419784ec4f8a32dd7b
Autor:
Danny M. Cohn, Emel Aygören‐Pürsün, Jonathan A. Bernstein, Henriette Farkas, William R. Lumry, Marcus Maurer, Andrea Zanichelli, Matthew Iverson, James Hao, Michael D. Smith, Christopher M. Yea, Paul K. Audhya, Marc A. Riedl
Publikováno v:
Clinical and Translational Allergy, Vol 13, Iss 9, Pp n/a-n/a (2023)
Abstract Background Hereditary angioedema (HAE) with C1‐inhibitor deficiency (HAE‐C1‐INH) is characterized by recurrent, debilitating episodes of swelling. Sebetralstat, an investigational oral plasma kallikrein inhibitor, demonstrated promisin
Externí odkaz:
https://doaj.org/article/fa5357d5066e444bb5ad301768e9507f
Publikováno v:
Journal of Materials Research and Technology, Vol 21, Iss , Pp 2532-2546 (2022)
During last few years, the Additive Manufacturing (AM) technology has increasingly attracted the interest of both industries and researchers. In such a context, the present paper deals with the analysis of specimens made of additively manufactured AI
Externí odkaz:
https://doaj.org/article/ce44fe3207d145298694ece9c9bd01e7
Autor:
Marcus Maurer, Markus Magerl, Emel Aygören-Pürsün, Konrad Bork, Henriette Farkas, Hilary Longhurst, Sorena Kiani‑Alikhan, Laurence Bouillet, Isabelle Boccon-Gibod, Mauro Cancian, Andrea Zanichelli, David Launay
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 18, Iss 1, Pp 1-12 (2022)
Abstract Background Hereditary angioedema (HAE) is characterized by potentially severe and life-threatening attacks of localized swelling. Prophylactic therapies are available, including attenuated androgens. Efficacy of attenuated androgens has not
Externí odkaz:
https://doaj.org/article/5c2ad1d8ea544b7b9d2fa3693dc729cb
Publikováno v:
Composites Part C: Open Access, Vol 9, Iss , Pp 100306- (2022)
The present paper aims to prove the size-effect independence of Hybrid Fiber-Reinforced RCC (HyFR-RCC) fracture toughness determined through the Modified Two-Parameter Model (MTPM). A micromechanical numerical model is applied to simulate the fractur
Externí odkaz:
https://doaj.org/article/77bcca44b91c4289995860870ca39c5c
Autor:
Irina Guryanova, Chiara Suffritti, Debora Parolin, Andrea Zanichelli, Nastassia Ishchanka, Ekaterina Polyakova, Mikhail Belevtsev, Francesca Perego, Marco Cicardi, Yulia Zharankova, Natalya Konoplya, Sonia Caccia, Antonio Gidaro
Publikováno v:
Clinical and Molecular Allergy, Vol 19, Iss 1, Pp 1-8 (2021)
Abstract Background Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare disease. Few states in developing countries have an adequate management of HAE, but none of them belongs to the former USSR area. This study analyses data
Externí odkaz:
https://doaj.org/article/2bdbd634c5f04df49a6a4ca22be184ec
Autor:
Roberta Parente, Silvio Sartorio, Luisa Brussino, Tiziana De Pasquale, Alessandra Zoli, Stefano Agolini, Ester Di Agosta, Paolina Quattrocchi, Paolo Borrelli, Donatella Bignardi, Angelica Petraroli, Riccardo Senter, Valentina Popescu Janu, Chiara Cogliati, Maria Domenica Guarino, Oliviero Rossi, Davide Firinu, Stefano Pucci, Giuseppe Spadaro, Massimo Triggiani, Mauro Cancian, Andrea Zanichelli
Publikováno v:
Vaccines, Vol 11, Iss 4, p 852 (2023)
Angioedema due to C1 inhibitor deficiency (AE-C1-INH) is a rare disease characterized by recurrent and unpredictable attacks of angioedema. Multiple trigger factors, including trauma, emotional stress, infectious diseases, and drugs, could elicit ang
Externí odkaz:
https://doaj.org/article/d1c637201d1c44279728738ede719329
Autor:
Livia Savarese, Maria Bova, Assunta Maiello, Angelica Petraroli, Ilaria Mormile, Mauro Cancian, Riccardo Senter, Andrea Zanichelli, Giuseppe Spadaro, Maria Francesca Freda
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)
Abstract Background Hereditary angioedema associated to C1 inhibitor deficiency (C1-INH-HAE) is a pathological condition characterized by episodes of subcutaneous swelling and it is frequently associated with discomfort and social impairment of the p
Externí odkaz:
https://doaj.org/article/e1619129abdb456388abe77d81dab097