Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Simona Donadei"'
Autor:
Sofia Giorgetti, Marta Marchesi, Giulia Chiesa, Vittorio Bellotti, Gina Gregorini, Sara Raimondi, Simona Donadei, Caterina Valetti, Monica Stoppini, Cinzia Parolini, Palma Mangione, Laura Obici, Giampaolo Merlini
Publikováno v:
Biochimica et Biophysica Acta-Molecular Basis of Disease
Biochimica et Biophysica Acta-Molecular Basis of Disease, Elsevier, 2010, 1812 (1), pp.87. ⟨10.1016/j.bbadis.2010.07.002⟩
Biochimica et Biophysica Acta-Molecular Basis of Disease, Elsevier, 2010, 1812 (1), pp.87. ⟨10.1016/j.bbadis.2010.07.002⟩
International audience; Hereditary systemic amyloidosis caused by apolipoprotein A-I variants is a dominantly inherited disease characterised by fibrillar deposits mainly localized in the kidneys, liver, testis and heart. We have previously shown tha
Autor:
Monica Stoppini, Massimo Stefani, Vittorio Rosti, Silvia Garagna, Vittorio Bellotti, Tui Neri, Carlo Alberto Redi, Giampaolo Merlini, Annalisa Relini, Maurizio Zuccotti, Sara Raimondi, Simona Donadei, Monica Bucciantini, Margherita Massa
Publikováno v:
Amyloid. 17:137-145
Regenerative medicine deals with the possible use of stem cells to repair tissues damaged by aging and related diseases, including amyloidoses. In the latter case, the toxicity of the amyloid deposits can, in principle, question the possibility to gr
Autor:
Tiziano Scalvini, Mariano Capistrano, Gina Gregorini, Laura Obici, Simona Donadei, Battista Fabio Viola, Claudia Izzi, Regina Tardanico, Francesco Scolari, Giampaolo Merlini, Christoph Röcken, L. Biasi
Publikováno v:
Journal of the American Society of Nephrology. 16:3680-3686
Apolipoprotein A-I amyloidosis is a rare, late-onset, autosomal dominant condition characterized by systemic deposition of amyloid in tissues, the major clinical problems being related to renal, hepatic, and cardiac involvement. Described is the clin
Autor:
Laura Obici, Giulia de Rosa, Marta Diegoli, Giovanni Palladini, Sabrina Marciano, A Demarchi, Simona Donadei, S. Coverlizza, Egidio Genovese, Giancarlo Ferrari, Eloisa Arbustini, Giampaolo Merlini, Vittorio Bellotti
Publikováno v:
Annals of Neurology. 58:639-644
Mutations in AβPP cause deposition of Aβ amyloid fibrils in brain parenchyma and cerebral vessels, resulting in Alzheimer's disease (AD) and/or cerebral amyloid angiopathy (CAA). We report a novel mutation (L705V) within the Aβ sequence of AβPP i
Autor:
Maddalena Marini, Tiziana Bosoni, Laura Verga, Simona Donadei, Gabriella Righetti, Remigio Moratti, Gabriele Sarais, Mario Nuvolone, Giampaolo Merlini, Riccardo Albertini, Simona Casarini, Maria Stella Graziani, Francesca Lavatelli, Gian Vico Melzi d’Eril, Laura Obici, Giovanni Palladini, Paola Russo
Publikováno v:
Clinical chemistry. 55(3)
Background: The diagnosis of systemic immunoglobulin light-chain (AL) amyloidosis requires demonstration of amyloid deposits in a tissue biopsy and amyloidogenic monoclonal light chains. The optimal strategy to identify the amyloidogenic clone has no
Autor:
Mario Mosconi, Carla Uggetti, Guido Moro, Laura Obici, Giovanni Montagna, Gennaro Esposito, Luigi Congi, Vittorio Bellotti, Giampaolo Merlini, Sara Raimondi, Simona Donadei, Monica Stoppini, Umberto Magrini, Giuseppe Villa, Sofia Giorgetti, Siro Segagni, Giovanni Galli, Annalisa Relini
Deposition of amyloid in the buttock is a rare complication of dialysis related amyloidosis (DRA), but this localization is even rarer in other types of amyloidoses. We report here the clinical, radiological, and biochemical features of a patient who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b71a391ab08a291313796ea2eb8b3feb
http://hdl.handle.net/11567/219802
http://hdl.handle.net/11567/219802
Autor:
Simonetta Falzoni, Simona Donadei, Marcello Govoni, Andrea Lo Monaco, Cinzia Pizzirani, Francesco Trotta, Francesco Di Virgilio, Renato La Corte
Publikováno v:
Scopus-Elsevier
OBJECTIVE IL-1beta plays a key role in the pathogenesis of Schnitzler's syndrome (SS). We have investigated inflammasome activity in peripheral blood mononuclear cells (PBMCs) from a patient affected by a variant type of SS. METHODS PBMCs were purifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::024209bbac5bf266b9b4cc38d21246bb
http://hdl.handle.net/11392/1378259
http://hdl.handle.net/11392/1378259
Autor:
T. Scalvini, G Merlini, L Obici, Laura Calabresi, Francesco Scolari, Simona Donadei, G Gregorini
Publikováno v:
XIth International Symposium on Amyloidosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e96c24b3eff7edd81de063fcba9c46d9
https://doi.org/10.1201/9781420043358.ch58
https://doi.org/10.1201/9781420043358.ch58
Autor:
G Merlini, L Obici, G Palladini, L Praderio, Sabrina Marciano, M Tresoldi, A Satta, Simona Donadei, A Cigni, F Lavatelli
Publikováno v:
Amyloid and Amyloidosis
Scopus-Elsevier
Amyloid and Amyloidosis ISBN: 9780429125249
Scopus-Elsevier
Amyloid and Amyloidosis ISBN: 9780429125249
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a4f004c0703c523cd509d428cb2ad6b
https://doi.org/10.1201/9781420037494.ch61
https://doi.org/10.1201/9781420037494.ch61
Autor:
Vittorio Perfetti, Giampaolo Merlini, C Bergonzi, Laura Verga, Giovanni Palladini, Sofia Giorgetti, Eloisa Arbustini, Laura Calabresi, Francesco Scolari, Simona Donadei, Gina Gregorini, Sabrina Marciano, Laura Obici, Vittorio Bellotti
Background & Aims: Hereditary systemic amyloidoses are autosomal dominant, late-onset disorders caused by mutations in the genes for a group of plasma proteins including transthyretin, lysozyme, fibrinogen Aα chain, gelsolin, apolipoprotein A-I, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e86cbcf91649cdd2bc90e254cf9f95d4
http://hdl.handle.net/11379/71050
http://hdl.handle.net/11379/71050