Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Francesco Arcoleo"'
Autor:
Mauro Cancian, Paola Triggianese, Stella Modica, Francesco Arcoleo, Donatella Bignardi, Luisa Brussino, Caterina Colangelo, Ester Di Agosta, Davide Firinu, Maria Domenica Guarino, Francesco Giardino, Marica Giliberti, Vincenzo Montinaro, Riccardo Senter
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionHereditary angioedema due to C1-inhibitor deficiency is influenced by hormonal factors, with a more severe course of disease in women. Our study aims to deepen the impact of puberty on onset, frequency, location and severity of attacks.Me
Externí odkaz:
https://doaj.org/article/952f860c14a44f08896c73d9c2d706ce
Autor:
Stefano ALIBERTI, Francesco AMATI, Anna ANNUNZIATA, Francesco ARCOLEO, Paolo BADERNA, Francesco BINI, Chiara F. CARRARO, Leonardo IANNACCI, Salvatore LO CICERO, Giovanni PASSALACQUA, Davide PILONI, Giulia SCIOSCIA, Christine SEEBACHER, Elisabetta SORTINO, Antonella SPACONE, Andrea VIANELLO
Publikováno v:
Minerva Respiratory Medicine. 61
Publikováno v:
Archives of Asthma, Allergy and Immunology. 4:009-011
Autor:
Marco Cicardi, Chiara Frigerio, Riccardo Senter, Maria Domenica Guarino, Itaca, Antonio Gidaro, Maria Bova, Francesco Arcoleo, Andrea Zanichelli, Tiziana De Pasquale, Mauro Cancian, Mariangela Lo Pizzo, Piergiorgio Duca, Francesca Perego
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice. 8:1772-1774
Autor:
Mauro Cancian, Stefania Loffredo, Giovanni Pellacani, Giovanni Rolla, Amato de Paulis, Filomena Maio, Luigi Giovanni Cremonte, Massimo Triggiani, Gianfranco Vitiello, Roberta Parente, Paola Parronchi, Riccardo Senter, Giuseppe Spadaro, Davide Firinu, Eustachio Nettis, Laura Bonzano, Maria Bova, Donatella Lamacchia, Elisa Boni, Francesco Arcoleo, Angelica Petraroli, Stefano Del Giacco, Luisa Brussino, Aikaterini Detoraki, Maria Rosaria Galdiero
Publikováno v:
AllergyREFERENCES. 76(7)
Background Orofacial granulomatosis (OFG) is characterized by granulomatous inflammation of the soft tissues of maxillofacial region. We explored OFG patients from 10 different Italian centers and summarized the most recent literature data. Methods A
The complex alteration in the network of IL-17-type cytokines in patients with hereditary angioedema
Autor:
Gabriella Misiano, Mariangela Lo Pizzo, Francesco Arcoleo, Giuseppina Colonna Romano, Salvatore Milano, Enrico Cillari, Vito M. R. Muggeo
Publikováno v:
Clinical and Experimental Medicine. 18:355-361
Hereditary angioedema (HAE) is a rare autosomic-dominant disorder characterized by a deficiency of C1 esterase inhibitor which causes episodic swellings of subcutaneous tissues, bowel walls and upper airways that are disabling and potentially life-th
Autor:
Hilary Longhurst, Francesco Arcoleo, D. Launay, T. Lobera, Shmuel Kivity, Pierre-Yves Jeandel, Marco Cicardi, Janne Björkander, Matthew Helbert, H. Maillard, C. Hernando de Larramendi, Avner Reshef, Efimia Papadopoulou-Alataki, Y. Graif, R. Lleonart, Olivier Fain, Andrea Bauer, T. Caballero, L. Bouillet, B. Sáenz de San Pedro, Alain Sobel, Gianni Marone, Teresa Caballero, W. Aberer, Elias Toubi, Brigitte Coppere, Murat Bas, Vincent Fabien, Andrea Zanichelli, Y. Ollivier, Maria L. Baeza, Anete Sevciovic Grumach, A. Masseau, Irmgard Andresen, Konrad Bork, Anette Bygum, Vincenzo Montinaro, Marcus Maurer, Fotis Psarros, Gisèle Kanny, Ludovic Martin, Rosario Cabañas, B. Goichot, Sophie Guez, I. Martinez, Werner Aberer, P. Manconi, Mar Guilarte, Anne Gompel, J. Arnolds, C. Blanchard Delaunay, Laurence Bouillet, Emel Aygören-Pürsün, D. Hernandez de Rojas
Publikováno v:
Zanichelli, A, Longhurst, H J, Maurer, M, Bouillet, L, Aberer, W, Fabien, V, Andresen, I, Caballero, T, IOS Study Group & Bygum, A 2016, ' Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting ', Annals of Allergy, Asthma, & Immunology, vol. 117, no. 4, pp. 394-398 . https://doi.org/10.1016/j.anai.2016.08.014
BACKGROUND: Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and upper airways and pain in the abdomen because of mucosal swelling. C1-INH-HAE is frequently misdiagnosed, leading to delays in diagnosis, in
Autor:
Giuseppina Colonna-Romano, Vito M. R. Muggeo, Francesco Arcoleo, Marilisa Salemi, V. Mandalà, Salvatore Milano, Gabriella Misiano, Enrico Cillari
Hereditary angioedema (HAE) is a rare autosomal dominant disorder, due to C1-inhibitor deficiency, which causes episodic swellings of subcutaneous tissues, bowel walls and upper airways which are disabling and potentially life-threatening. We evaluat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53619fe625a3f725c8cbe6650be3cf84
http://hdl.handle.net/10447/224470
http://hdl.handle.net/10447/224470
Publikováno v:
La Rivista Italiana della Medicina di Laboratorio - Italian Journal of Laboratory Medicine. 8:131-137
L’angioedema ereditario e causato da una carenza genetica di C1-inibitore, fattore che regola una serie di pathways infiammatori. I pazienti affetti da HAE hanno crisi intermittenti caratterizzate da edemi cutanei o mucosali legati a un malfunziona
PREVALENCE OF ANTIBODIES ANTI-BARTONELLA HENSELAEIN WESTERN SICILY: CHILDREN, BLOOD DONORS, AND CATS
Autor:
Salvatore Di Rosa, Francesco Arcoleo, Maria Francesca Di Gregorio, Anna Micalizzi, Giustina Vitale, Ilenia Pepe, Floriana Bonura, Letizia Palillo, Enrico Cillari, Giovam Battista Rini, Affronti M, Pasquale Mansueto, Aurelio Seidita
Publikováno v:
Journal of Immunoassay and Immunochemistry. 33:18-25
To evaluate seroprevalence of B. henselae infection both in Sicilian children and healthy blood donors. Furthermore, circulation of Bartonella in the natural reservoir was also studied. Two hundred forty-three children, living in Sicily (Palermo), af