Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Tauro, Maria"'
Autor:
Di Leo, Milena, Bianco, Margherita, Zuppardo, Raffaella Alessia, Guslandi, Mario, Calabrese, Federica, Mannucci, Alessandro, Neri, Tauro Maria, Testoni, Pier Alberto, Leandro, Gioacchino, Cavestro, Giulia Martina
Publikováno v:
In Digestive and Liver Disease August 2017 49(8):847-853
Publikováno v:
Frontiers in Immunology, Vol 5 (2014)
ANCA-associated vasculitis (AAV) is a group of disorders that is caused by inflammation affecting small blood vessels. Both arteries and veins are affected. AAV includes microscopic polyangiitis (MPA), granulomatosis with polyangiitis (GPA) renamed f
Externí odkaz:
https://doaj.org/article/d3deba1e8b6c49a98e65a7ca73d36f41
Autor:
Pier Alberto Testoni, Alessandro Mannucci, Milena Di Leo, Margherita Bianco, Raffaella Alessia Zuppardo, G. Leandro, F Calabrese, Tauro Maria Neri, Giulia Martina Cavestro, Mario Guslandi
Publikováno v:
Digestive and Liver Disease. 49:847-853
Background SPINK1 p.N34S gene variation is one of the endogenous factors which seem to be associated with chronic pancreatitis (CP). However, in literature there is no clear agreement regarding its contribution in different ethnicity and CP etiologie
Autor:
Bertelli, Roberta, Ginevri, Fabrizio, Caridi, Gianluca, Dagnino, Monica, Sandrini, Silvio, Di Duca, Marco, Emma, Francesco, Sanna-Cherchi, Simone, Scolari, Francesco, Neri, Tauro Maria, Murer, Luisa, Massella, Laura, Basile, Giancarlo, Rizzoni, Gianfranco, Perfumo, Francesco, Ghiggeri, Gian Marco *
Publikováno v:
In American Journal of Kidney Diseases June 2003 41(6):1314-1321
Autor:
Lucchini, Diana, Giampaolo, Rebecca, Fogazzi, Gianluca, Tauro, Maria, Buffoli, Alberto, Girardi, Veronica, Ruzzenenti, Nella, Civilotti, Cristina
Publikováno v:
Psicologia Della Salute; 2020, Issue 3, p5-34, 30p
Autor:
Nadia Naldi, Tauro Maria Neri, A. Zerbini, Diletta Laccabue, Roberta Camisa, Fotios Loupakis, N. Chernyschova, Gabriele Missale, Beatrice Bortesi, Francesca Negri, Annamaria Ruzzo, Antonino Musolino, Andrea Ardizzoni, Giancarlo Bisagni
Publikováno v:
The Pharmacogenomics Journal. 14:14-19
Antibody-dependent cellular cytotoxicity (ADCC), which is activated by effector cells via immunoglobulin G (IgG) fragment C receptors (FcRs), was proposed as a mechanism of cetuximab efficacy. Peripheral blood mononuclear cells (PBMCs) from 23 health
Autor:
G. Rodorigo, M. L. Serino, L. Ippolito, S. Macchi, Lelia Valdrè, Chiara Biasoli, P. Pedrazzi, D. Vincenzi, Annarita Tagliaferri, Davide Martorana, M. Savi, M. Volta, M. D'Incà, C. Di Perna, Tauro Maria Neri, Gianna Franca Rivolta, Federica Riccardi, M. C. Arbasi
Publikováno v:
Haemophilia. 16:791-800
Summary. Haemophilia A (HA) is an X-linked recessive bleeding disorder caused by a lack or decrease of coagulation factor VIII activity. The molecular diagnosis of HA is challenging and a variety of different mutations have been identified throughout
Autor:
Annarita Tagliaferri, Roberta La Starza, Simonetta Rosato, Livia Garavelli, Tauro Maria Neri, Gianna Franca Rivolta, Federica Riccardi, Francesca Romana Grati, Gabriele Quintavalle, Caterina Di Perna, Davide Martorana, Gabriella Sammarelli, Livia Marcato, Vera Uliana
Publikováno v:
Cytogenetic and genome research. 147(1)
Variations of DNA sequences in the human genome range from large, microscopically visible chromosome anomalies to single nucleotide changes. Submicroscopic genomic copy number variations, i.e. chromosomal imbalances which are undetectable by conventi
Autor:
Benedetta, Pellegrino, Mariangela, Bella, Maria, Michiara, Paola, Zanelli, Nadia, Naldi, Rosa, Porzio, Beatrice, Bortesi, Daniela, Boggiani, Daniele, Zanoni, Roberta, Camisa, Tauro Maria, Neri, Carmine, Pinto, Antonino, Musolino
Publikováno v:
Acta bio-medica : Atenei Parmensis. 87(1)
BRCA1/2 mutation carriers diagnosed with breast cancer have a strong life-time risk of developing contralateral breast cancer (CBC). We performed a population-based study with the aim of estimating the proportion of CBC associated with BRCA1/BRCA2 mu
Autor:
Davide Martorana, Isabella Viani, Francesco Tassi, Lucia Ghizzoni, Tauro Maria Neri, Maria E. Street, Roberta Minari, Sergio Bernasconi, Alessandra Vottero
Publikováno v:
Scopus-Elsevier
OBJECTIVE: Congenital adrenal hypoplasia (CAH) is a rare disorder that can be inherited in an X-linked or autosomal recessive pattern. CAH is frequently associated with hypogonadotropic hypogonadism (HHG) with absent or arrested puberty and impaired
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24aa1aeb124bc22c17b0b4c47e2b1cbe
http://hdl.handle.net/2318/1659874
http://hdl.handle.net/2318/1659874