Zobrazeno 1 - 10
of 190
pro vyhledávání: '"Ugo Ramenghi"'
Autor:
Giuseppe Palumbo, Piero Farruggia, Ugo Ramenghi, Giovanna Russo, Alessandra Borchiellini, Marco Spinelli, Carlo Dufour, Fiorina Giona, Saverio Ladogana, Marco Zecca, Silverio Perrotta, Andrea Pession, Paola Giordano
Publikováno v:
Hematology, Vol 28, Iss 1 (2023)
ABSTRACTBackground Immune thrombocytopenia (ITP) is the most common acquired bleeding disorder. In both children and adults, the primary goal of any therapeutic approach consists of cessation of bleeding and its prevention. Several options are curren
Externí odkaz:
https://doaj.org/article/86ebea6f16584e74b5c230cc3fda77be
Autor:
Silvia Garazzino, Marco Denina, Giulia Pruccoli, Elisa Funiciello, Ugo Ramenghi, Franca Fagioli
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-3 (2023)
Abstract Post-COVID condition is a new and highly debated entity that is still to be outlined in its complexity, especially in the pediatric population. In response to the article by Trapani and colleagues, we report the results of a long-term follow
Externí odkaz:
https://doaj.org/article/3aefe8b856b641349cc5935e5db868d6
Autor:
Elena Palmisani, Maurizio Miano, Alice Grossi, Marina Lanciotti, Michela Lupia, Paola Terranova, Isabella Ceccherini, Eugenia Montanari, Michaela Calvillo, Filomena Pierri, Concetta Micalizzi, Rosario Maggiore, Daniela Guardo, Sabrina Zanardi, Elena Facchini, Angela Maggio, Elena Mastrodicasa, Paola Corti, Giovanna Russo, Marta Pillon, Piero Farruggia, Simone Cesaro, Angelica Barone, Francesca Tosetti, Ugo Ramenghi, Nicoletta Crescenzio, Jack Bleesing, Carlo Dufour, Francesca Fioredda
Publikováno v:
HemaSphere, Vol 7, Iss 3, p e845 (2023)
Autoimmune lymphoproliferative syndrome (ALPS) is an inherited disorder of lymphocyte homeostasis classically due to mutation of FAS, FASL, and CASP10 genes (ALPS-FAS/CASP10). Despite recent progress, about one-third of ALPS patients does not carry c
Externí odkaz:
https://doaj.org/article/c43c1c5cbfe24a589e2d78a06dda00dd
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-4 (2021)
Abstract Background We report a pediatric patient presenting in good general condition despite a hemoglobin value of 1,9 g/dL, which is normally regarded as life-threatening. Case presentation An African 5 years-old girl presented to our Emergency De
Externí odkaz:
https://doaj.org/article/321ed2b00ffd4649a57cd969632e3571
Autor:
Carmelo Carmona-Rivera, Yu Zhang, Kerry Dobbs, Tovah E. Markowitz, Clifton L. Dalgard, Andrew J. Oler, Dillon R. Claybaugh, Deborah Draper, Meng Truong, Ottavia M. Delmonte, Francesco Licciardi, Ugo Ramenghi, Nicoletta Crescenzio, Luisa Imberti, Alessandra Sottini, Virginia Quaresima, Chiara Fiorini, Valentina Discepolo, Andrea Lo Vecchio, Alfredo Guarino, Luca Pierri, Andrea Catzola, Andrea Biondi, Paolo Bonfanti, Maria C. Poli Harlowe, Yasmin Espinosa, Camila Astudillo, Emma Rey-Jurado, Cecilia Vial, Javiera de la Cruz, Ricardo Gonzalez, Cecilia Pinera, Jacqueline W. Mays, Ashley Ng, Andrew Platt, NIH COVID Autopsy Consortium, COVID STORM Clinicians, Beth Drolet, John Moon, Edward W. Cowen, Heather Kenney, Sarah E. Weber, Riccardo Castagnoli, Mary Magliocco, Michael A. Stack, Gina Montealegre, Karyl Barron, Danielle L. Fink, Douglas B. Kuhns, Stephen M. Hewitt, Lisa M. Arkin, Daniel S. Chertow, Helen C. Su, Luigi D. Notarangelo, Mariana J. Kaplan
Publikováno v:
JCI Insight, Vol 7, Iss 16 (2022)
Dysregulation in neutrophil extracellular trap (NET) formation and degradation may play a role in the pathogenesis and severity of COVID-19; however, its role in the pediatric manifestations of this disease, including multisystem inflammatory syndrom
Externí odkaz:
https://doaj.org/article/9966f052157547d38c7511014127ae57
Autor:
Angela Guarina, Maddalena Marinoni, Giuseppe Lassandro, Paola Saracco, Silverio Perrotta, Elena Facchini, Lucia Dora Notarangelo, Giovanna Russo, Paola Giordano, Francesca Romano, Giuseppe Bertoni, Chiara Gorio, Gabriela Boscarol, Milena Motta, Marco Spinelli, Angelica Barone, Marco Zecca, Francesca Compagno, Saverio Ladogana, Angela Maggio, Maurizio Miano, Gianluca DellOrso, Elena Chiocca, Ilaria Fotzi, Angela Petrone, Assunta Tornesello, Irene D'Alba, Silvia Salvatore, Maddalena Casale, Giuseppe Puccio, Ugo Ramenghi, Piero Farruggia
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 3, Pp 175-180 (2021)
Objective: The association between celiac disease (CD) and immune thrombocytopenia (ITP) is still uncertain. The aim of this study was to characterize the coexistence of these two diseases in Italian children. Materials and Methods: This is a retrosp
Externí odkaz:
https://doaj.org/article/8f02b3e4ac11429384ebd27a97ba246a
Autor:
Giovanni Del Borrello, Maurizio Miano, Concetta Micalizzi, Michela Lupia, Isabella Ceccherini, Alice Grossi, Andrea Cavalli, Stefano Gustincich, Marta Rusmini, Maura Faraci, Gianluca Dell’Orso, Ugo Ramenghi, Alessio Mesini, Erica Ricci, Maurizio Schiavone, Natascia Di Iorgi, Carlo Dufour
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Cartilage-hair hypoplasia (CHH) is a syndromic immunodeficiency characterized by metaphyseal dysplasia, cancer predisposition, and varying degrees of anemia. It may present as severe combined immunodeficiency in infancy, or slowly progress until full
Externí odkaz:
https://doaj.org/article/8eef0c2569d74cd783e611f2be171661
Autor:
Peter D. Burbelo, Riccardo Castagnoli, Chisato Shimizu, Ottavia M. Delmonte, Kerry Dobbs, Valentina Discepolo, Andrea Lo Vecchio, Alfredo Guarino, Francesco Licciardi, Ugo Ramenghi, Emma Rey-Jurado, Cecilia Vial, Gian Luigi Marseglia, Amelia Licari, Daniela Montagna, Camillo Rossi, Gina A. Montealegre Sanchez, Karyl Barron, Blake M. Warner, John A. Chiorini, Yazmin Espinosa, Loreani Noguera, Lesia Dropulic, Meng Truong, Dana Gerstbacher, Sayonara Mató, John Kanegaye, Adriana H. Tremoulet, Pediatric Emergency Medicine Kawasaki Group, Eli M. Eisenstein, Helen C. Su, Luisa Imberti, Maria Cecilia Poli, Jane C. Burns, Luigi D. Notarangelo, Jeffrey I. Cohen, Naomi Abe, Amy Bryl, J. Joelle Donofrio-Odmann, Atim Ekpenyong,, Michael Gardiner,, David J. Gutglass, Margaret B. Nguyen, Stacey Ulrich
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The antibody profile against autoantigens previously associated with autoimmune diseases and other human proteins in patients with COVID-19 or multisystem inflammatory syndrome in children (MIS-C) remains poorly defined. Here we show that 30% of adul
Externí odkaz:
https://doaj.org/article/b3511accec79439ab5ec278ade02c5be
Autor:
Annalisa Lonetti, Valentina Indio, Irma Dianzani, Ugo Ramenghi, Lydie Da Costa, Dagmar Pospíšilová, Anna Rita Migliaccio
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
NR3C1, the gene encoding the glucocorticoid receptor, is polymorphic presenting numerous single nucleotide polymorphisms (SNPs) some of which are emerging as leading cause in the variability of manifestation and/or response to glucocorticoids in huma
Externí odkaz:
https://doaj.org/article/1462818fb870486fb96eee9b1dedf86e
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Externí odkaz:
https://doaj.org/article/970df23f3eca480fa60ebbf73e50f068