Zobrazeno 1 - 10
of 132
pro vyhledávání: '"Lucia, Dora Notarangelo"'
Autor:
Elena Sophia Fratini, Maddalena Migliavacca, Federica Barzaghi, Claudia Fossati, Stefania Giannelli, Ilaria Monti, Miriam Casiraghi, Francesca Ferrua, Salvatore Recupero, Giulia Consiglieri, Valeria Calbi, Francesca Tucci, Vera Gallo, Maria Ester Bernardo, Sabina Cenciarelli, Monica Palmoni, Margherita Moni, Luca Galimberti, Marzia Duse, Lucia Leonardi, Elena Sieni, Elena Soncini, Fulvio Porta, Lucia Dora Notarangelo, Raffaella De Santis, Saverio Ladogana, Alessandro Aiuti, Maria Pia Cicalese
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Hemophagocytic inflammatory syndrome (HIS) is a rare form of secondary hemophagocytic lymphohistiocytosis caused by an impaired equilibrium between natural killer and cytotoxic T-cell activity, evolving in hypercytokinemia and multiorgan failure. In
Externí odkaz:
https://doaj.org/article/7c36f84d68d64741ac3146f248b26d26
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:
Jessica Galli, Lorenzo Pinelli, Serena Micheletti, Giovanni Palumbo, Lucia Dora Notarangelo, Vassilios Lougaris, Laura Dotta, Elisa Fazzi, Raffaele Badolato
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Background Warts Hypogammaglobulinemia Immunodeficiency Myelokathexis (WHIM) syndrome is a primary immunodeficiency characterized by recurrent bacterial infections, severe chronic neutropenia, with lymphopenia, monocytopenia and myelokathexi
Externí odkaz:
https://doaj.org/article/7240e706dfe24179aaf0127aea415ee2
Autor:
Maddalena Casale, Gian Luca Forni, Elena Cassinerio, Daniela Pasquali, Raffaella Origa, Marilena Serra, Saveria Campisi, Angelo Peluso, Roberta Renni, Alessandro Cattoni, Elisa De Michele, Massimo Allò, Maurizio Poggi, Francesca Ferrara, Rosanna Di Concilio, Filomena Sportelli, Antonella Quarta, Maria Caterina Putti, Lucia Dora Notarangelo, Antonella Sau, Saverio Ladogana, Immacolata Tartaglione, Stefania Picariello, Alessia Marcon, Patrizia Sturiale, Domenico Roberti, Antonio Ivan Lazzarino, Silverio Perrotta
Publikováno v:
Haematologica, Vol 107, Iss 2 (2021)
Transfusion-dependent patients typically develop iron-induced cardiomyopathy, liver disease, and endocrine complications. We aimed to estimate the incidence of endocrine disorders in transfusiondependent thalassemia (TDT) patients during long-term ir
Externí odkaz:
https://doaj.org/article/4f1b5fff7e4d48f6bf1a9742f7e60cc3
Autor:
Paola Giordano, Giuseppe Lassandro, Angelica Barone, Simone Cesaro, Ilaria Fotzi, Fiorina Giona, Saverio Ladogana, Maurizio Miano, Antonio Marzollo, Margherita Nardi, Lucia Dora Notarangelo, Andrea Pession, Antonio Ruggiero, Giovanna Russo, Paola Saracco, Marco Spinelli, Alessandra Tolva, Assunta Tornesello, Valentina Palladino, Giovanni Carlo Del Vecchio
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Background: The thrombopoietin receptor agonist eltrombopag has been shown to be safe and effective for children with chronic immune thrombocytopenia (ITP). The aim of the present study was to characterize eltrombopag use in current clinical practice
Externí odkaz:
https://doaj.org/article/c74766bb01034e7ba185c04a4b7a3c49
Autor:
Giorgio Piccinelli, Francesca Caccuri, Elena De Peri, Andrea Tironi, Silvia Odolini, Lucia Dora Notarangelo, Franco Gargiulo, Francesco Castelli, Nicola Latronico, Fabio Facchetti, Arnaldo Caruso
Publikováno v:
International Journal of Infectious Diseases, Vol 72, Iss , Pp 3-5 (2018)
Capnocytophaga canimorsus infection was recently recognized as a zoonosis. We report the first case of fulminant septic shock in Italy caused by this pathogen. The patient, with a history of splenectomy, died at the main hospital in Brescia with a pr
Externí odkaz:
https://doaj.org/article/850ea6693d30432690be72147e882f3a
Autor:
Marianna Maffeis, Lucia Dora Notarangelo, Richard Fabian Schumacher, Elena Soncini, Annarosa Soresina, Arnalda Lanfranchi, Fulvio Porta
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Background and aims: Primary immunodeficiencies (PID) are characterized by recurrent infections and increased risk of malignancies because of the reduced immunological surveillance against cancer cells and oncogenic viruses.Methods: We report the inc
Externí odkaz:
https://doaj.org/article/9a0653b27dfa49be9959b9eb7b760c57
Autor:
Laura Cristina Gironi, Francesca Zottarelli, Gianfranco Savoldi, Lucia Dora Notarangelo, Maria Eleonora Basso, Ivana Ferrero, Fabio Timeus, Franca Fagioli, Luigi Maiuri, Enrico Colombo, Paola Savoia
Publikováno v:
Medicina, Vol 55, Iss 3, p 78 (2019)
The term congenital hypopigmentary disorders refers to a wide group of heterogeneous hereditary diseases, clinically characterized by inborn pigmentary defects of the iris, hair, and/or skin. They include Gray Hair Syndromes (GHSs), a rare group of a
Externí odkaz:
https://doaj.org/article/40f658ecd3794c27bf4f696041dc2c16
Autor:
Ezio, Zanon, Samantha, Pasca, Gianluca, Sottilotta, Angelo C, Molinari, Antonietta, Ferretti, Patrizia, Di Gregorio, Berardino, Pollio, Michele, Pizzuti, Lucia Dora, Notarangelo, Chiara, Biasoli, Piergiorgio, Cojutti, Federico, Pea, Paolo, Simioni, Flora, Peyvandi
Publikováno v:
Blood transfusion = Trasfusione del sangue.
Congenital factor XIII (FXIII) deficiency is a rare coagulation disorder characterized by muscular or mucocutaneous bleeding with life-threatening intracranial hemorrhages (ICHs), especially in cases with severe disease. The best treatment is the use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b9eb70b133a7e438c4d4b981785ca415
https://pubmed.ncbi.nlm.nih.gov/36580025
https://pubmed.ncbi.nlm.nih.gov/36580025
Autor:
Désirée Caselli, Laura Sainati, Ilaria Capolsini, Annalisa Condorelli, Lucia Dora Notarangelo, Paola Corti, Giovanna Russo, Francesca Romano, Gianluca Boscarol, Elisa Bertoni, Paola Giordano, Silvia Fasoli, Fiorina Giona, Matteo Maruzzi, Piera Samperi, Vincenzo Guardabasso, Raffaella Colombatti, Fabio Tucci, Ugo Ramenghi, Maddalena Marinoni, Maria Luisa Casciana, Elena Facchini, Cristina Pizzato
Publikováno v:
Annals of Hematology. 99:413-420
Oral ferrous salts are standard treatment for children with iron deficiency anemia (IDA). The objective of our study was to monitor oral iron therapy in children, aged 3 months-12 years, with IDA. We prospectively collected clinical and hematological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a26cc2879ab2e112028c3ee035afe2b8
https://doi.org/10.1007/s00277-020-03906-w
https://doi.org/10.1007/s00277-020-03906-w