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Update on α1-antitrypsin deficiency.
Ferrarotti I, Ottaviani S, De Silvestri A, Corsico AG. Ferrarotti I, et al. Among authors: de silvestri a. Breathe (Sheff). 2018 Jun;14(2):e17-e24. doi: 10.1183/20734735.015018. Breathe (Sheff). 2018. PMID: 30131830 Free PMC article. Review.
Complement receptor 1 gene polymorphisms are associated with idiopathic pulmonary fibrosis.
Zorzetto M, Ferrarotti I, Trisolini R, Lazzari Agli L, Scabini R, Novo M, De Silvestri A, Patelli M, Martinetti M, Cuccia M, Poletti V, Pozzi E, Luisetti M. Zorzetto M, et al. Among authors: de silvestri a. Am J Respir Crit Care Med. 2003 Aug 1;168(3):330-4. doi: 10.1164/rccm.200302-221OC. Epub 2003 May 28. Am J Respir Crit Care Med. 2003. PMID: 12773320
Case-finding for alpha1-antitrypsin deficiency in Kazakh patients with COPD.
Zhumagaliyeva A, Ottaviani S, Greulich T, Gorrini M, Vogelmeier C, Karazhanova L, Nurgazina G, DeSilvestri A, Kotke V, Barzon V, Zorzetto M, Corsico A, Ferrarotti I. Zhumagaliyeva A, et al. Multidiscip Respir Med. 2017 Oct 25;12:23. doi: 10.1186/s40248-017-0104-5. eCollection 2017. Multidiscip Respir Med. 2017. PMID: 29090095 Free PMC article.
Inhaled recombinant GM-CSF reduces the need for whole lung lavage and improves gas exchange in autoimmune pulmonary alveolar proteinosis patients.
Campo I, Carey BC, Paracchini E, Kadija Z, De Silvestri A, Rodi G, De Amici M, Torre C, Zorzetto M, Griese M, Meloni F, Corsico AG, Trapnell BC, Mariani F. Campo I, et al. Among authors: de silvestri a, de amici m. Eur Respir J. 2024 Jan 4;63(1):2301233. doi: 10.1183/13993003.01233-2023. Print 2024 Jan. Eur Respir J. 2024. PMID: 37973175 Free PMC article. Clinical Trial.
Gender Differences at the Onset of Autoimmune Thyroid Diseases in Children and Adolescents.
Calcaterra V, Nappi RE, Regalbuto C, De Silvestri A, Incardona A, Amariti R, Bassanese F, Clemente AM, Vinci F, Albertini R, Larizza D. Calcaterra V, et al. Among authors: de silvestri a. Front Endocrinol (Lausanne). 2020 Apr 17;11:229. doi: 10.3389/fendo.2020.00229. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32362875 Free PMC article.
Phenotypic spectrum of short-chain enoyl-Coa hydratase-1 (ECHS1) deficiency.
Masnada S, Parazzini C, Bini P, Barbarini M, Alberti L, Valente M, Chiapparini L, De Silvestri A, Doneda C, Iascone M, Saielli LA, Cereda C, Veggiotti P, Corbetta C, Tonduti D. Masnada S, et al. Among authors: de silvestri a. Eur J Paediatr Neurol. 2020 Sep;28:151-158. doi: 10.1016/j.ejpn.2020.07.007. Epub 2020 Jul 29. Eur J Paediatr Neurol. 2020. PMID: 32800686
A case report on filamin A gene mutation and progressive pulmonary disease in an infant: A lung tissued derived mesenchymal stem cell study.
Calcaterra V, Avanzini MA, Mantelli M, Agolini E, Croce S, De Silvestri A, Re G, Collura M, Maltese A, Novelli A, Pelizzo G. Calcaterra V, et al. Among authors: de silvestri a. Medicine (Baltimore). 2018 Dec;97(50):e13033. doi: 10.1097/MD.0000000000013033. Medicine (Baltimore). 2018. PMID: 30557962 Free PMC article.
334 results