Zobrazeno 1 - 10
of 533
pro vyhledávání: '"Cancrini C."'
Akademický článek
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Autor:
Rivalta, B., Attardi, E., Cifaldi, C., Rosti, V., Pacillo, L., Hajrullaj, H., Di Cesare, S., Amodio, D., Algeri, M., Luciani, M., Barzaghi, F., Finocchi, A., Di Matteo, G., Aiuti, A., Locatelli, F., Voso, M. T., Palumbo, G., Cancrini, C.
Publikováno v:
British Journal of Haematology; Jan2024, Vol. 204 Issue 1, pe6-e10, 5p
Autor:
T Blaine Crowley 1, Donna McDonald McGinn, 1, E Sullivan 2, K, 2 COVID group report Collaborators, Iq, Cancrini, C, Andrew, G, Dinakantha, K, Donna McDonald McGinn, Solveig, O, Alex, R, Kathleen, Es, Elfi, V
Publikováno v:
Journal of Clinical Immunology. 42:746-748
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c47a2429e2cf9be37c36678516586f7e
https://doi.org/10.1007/s10875-022-01246-0
https://doi.org/10.1007/s10875-022-01246-0
Akademický článek
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Autor:
Pacillo, L, Giardino, G, Amodio, D, Giancotta, C, Rivalta, B, Rotulo, Ga, Manno, Ec, Cifaldi, C, Palumbo, G, Pignata, C, Palma, P, Rossi, P, Finocchi, A, Cancrini, C
Publikováno v:
Frontiers in Immunology. 13
Primary Immunodeficiencies (PID) are a group of rare congenital disorders of the immune system. Autoimmune cytopenia (AIC) represents the most common autoimmune manifestation in PID patients. Treatment of AIC in PID patients can be really challenging
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c4b59914b94394526ba212b06d1a99d
https://doi.org/10.3389/fimmu.2022.911385
https://doi.org/10.3389/fimmu.2022.911385
Autor:
Leonardi, L, La Torre, F, Soresina, A, Federici, S, Cancrini, C, Castagnoli, R, Cinicola, B, Corrente, S, Giardino, G, Lougaris, V, Volpi, S, Marseglia, G, Cardinale, F, Immunology Task Force of the Italian Society of Pediatric Allergy and Immunology (SIAIP)
The complement system plays an essential role in both innate and adaptive immune responses. Any dysregulation in this system can disturb normal host defense and alter inflammatory response leading to both infections and autoimmune diseases. The compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da8c23a370cc55efb2953aa2a7b90af2
http://hdl.handle.net/11573/1639142
http://hdl.handle.net/11573/1639142
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
La Torre, F, Leonardi, L, Giardino, G, Volpi, S, Federici, S, Soresina, A, Cancrini, C, Lougaris, V, Castagnoli, R, Corrente, S, Cardinale, F, Immunology Commission of the Italian Society of Pediatric Allergy, I
Publikováno v:
Pediatric Allergy and Immunology
COVID‐19 is a complex new viral disease, in which a strict balance between anti‐viral immune response and the ensuing organ inflammation has a critical role in determining the clinical course. In adults, compelling evidence exists indicating that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e256e201d40d66fa5cc3ce0f0030827d
http://hdl.handle.net/11567/1034765
http://hdl.handle.net/11567/1034765
Autor:
Cinicola, B, Corrente, S, Castagnoli, R, Lougaris, V, Giardino, G, Leonardi, L, Volpi, S, La Torre, F, Federici, S, Soresina, A, Cancrini, C, Marseglia, G, Cardinale, F, Immunology Task Force of the Italian Society of Pediatric Allergy, I
Publikováno v:
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology. 33
Primary atopic disorders (PADs) are monogenic diseases characterized by allergy or atopy-related symptoms as fundamental features. In patients with PADs, primary immune deficiency and immune dysregulation symptoms are usually coexist. Chronic skin di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16e9dc409c134e9043ed41bbef28d94e
https://pubmed.ncbi.nlm.nih.gov/35080318
https://pubmed.ncbi.nlm.nih.gov/35080318
Autor:
Lega, S, Pin, A, Arrigo, S, Cifaldi, C, Girardelli, M, Bianco, A, Malamisura, M, Angelino, G, Faraci, S, Romeo, E F, Papadatou, B, Miano, M, Aloi, M, Magazzù, G, Romano, C, Calvo, P, Barabino, A, Martelossi, S, Tommasini, A, Di Matteo, G, Cancrini, C, De Angelis, P, Finocchi, A, Bramuzzo, M
Background and aims Multiple monogenic disorders present as very early onset inflammatory bowel disease (VEO-IBD) or as IBD with severe and atypical features. Establishing a genetic diagnosis may change patients’ management and prognosis. In this s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8df1e3e15e75e10fe6887f0fb0834cab
https://hdl.handle.net/11368/2957797
https://hdl.handle.net/11368/2957797