オープン アクセスを義務付けられた論文 - Alessandro Plebani詳細
一般には非公開: 10 件
B cell–helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen
I Puga, M Cols, CM Barra, B He, L Cassis, M Gentile, L Comerma, ...
Nature immunology 13 (2), 170-180, 2012
委任: US National Institutes of Health, Government of Spain
Mutational analysis of human BLyS in patients with common variable immunodeficiency
CG Losi, U Salzer, R Gatta, V Lougaris, G Cattaneo, A Meini, A Soresina, ...
Journal of clinical immunology 26, 396-399, 2006
委任: German Research Foundation
Paediatric MAS/HLH caused by a novel monoallelic activating mutation in p110δ
V Lougaris, M Baronio, A Castagna, G Tessarin, S Rossi, L Gazzurelli, ...
Clinical Immunology 219, 108543, 2020
委任: Government of Italy
Monoallelic BAFFR P21R/H159Y mutations and familiar primary antibody deficiencies
V Lougaris, M Baronio, D Moratto, F Cardinale, A Plebani
Journal of clinical immunology 36 (1), 1-3, 2016
委任: Government of Italy
Autosomal recessive agammaglobulinemia: the third case of Igβ deficiency due to a novel non-sense mutation
V Lougaris, M Vitali, M Baronio, D Moratto, G Tampella, A Biasini, ...
Journal of clinical immunology 34, 425-427, 2014
委任: Government of Italy
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients
V Lougaris, M Baronio, S Masneri, T Lorenzini, K Cattivelli, G Tampella, ...
Clinical Immunology 163, 10-13, 2016
委任: Government of Italy
Lymphocyte alterations in patients with common variable immunodeficiency (CVID) and autoimmune manifestations
S Rossi, M Baronio, L Gazzurelli, G Tessarin, G Baresi, M Chiarini, ...
Clinical Immunology 241, 109077, 2022
委任: Government of Italy
Lack of DOCK8 impairs the primary biologic functions of human NK cells and abrogates CCR7 surface expression in a WASP-independent manner
O Patrizi, M Baronio, L Gazzurelli, S Rossi, S Rezzola, E Marcenaro, ...
Clinical Immunology 237, 108974, 2022
委任: Government of Italy
Immunological evaluation of patients affected with Jacobsen syndrome reveals profound not age-related lymphocyte alterations
M Baronio, F Saettini, L Gazzurelli, S Rossi, A Marzollo, S Ricci, D Zama, ...
Journal of Clinical Immunology, 1-10, 2022
委任: Government of Italy
μ Heavy Chain Deficiency
V Lougaris, A Plebani
Encyclopedia of Medical Immunology: Immunodeficiency Diseases, 490-492, 2020
委任: US National Institutes of Health
一般公開: 78 件
The EUROclass trial: defining subgroups in common variable immunodeficiency
C Wehr, T Kivioja, C Schmitt, B Ferry, T Witte, E Eren, M Vlkova, ...
Blood, The Journal of the American Society of Hematology 111 (1), 77-85, 2008
委任: German Research Foundation
A Homozygous CARD9 Mutation in a Family with Susceptibility to Fungal Infections
EO Glocker, A Hennigs, M Nabavi, AA Schäffer, C Woellner, U Salzer, ...
New England Journal of Medicine 361 (18), 1727-1735, 2009
委任: US National Institutes of Health, German Research Foundation
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity
G Lopez-Herrera, G Tampella, Q Pan-Hammarström, P Herholz, ...
The American Journal of Human Genetics 90 (6), 986-1001, 2012
委任: US National Institutes of Health, Swedish Research Council
Immunoglobulin D enhances immune surveillance by activating antimicrobial, proinflammatory and B cell–stimulating programs in basophils
K Chen, W Xu, M Wilson, B He, NW Miller, E Bengten, ES Edholm, ...
Nature immunology 10 (8), 889-898, 2009
委任: US National Institutes of Health
ICOS deficiency is associated with a severe reduction of CXCR5+ CD4 germinal center Th cells
L Bossaller, J Burger, R Draeger, B Grimbacher, R Knoth, A Plebani, ...
The Journal of Immunology 177 (7), 4927-4932, 2006
委任: German Research Foundation
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects
C Schwab, A Gabrysch, P Olbrich, V Patiño, K Warnatz, D Wolff, ...
Journal of Allergy and Clinical Immunology 142 (6), 1932-1946, 2018
委任: US National Institutes of Health, German Research Foundation, UK …
The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88
B He, R Santamaria, W Xu, M Cols, K Chen, I Puga, M Shan, H Xiong, ...
Nature immunology 11 (9), 836-845, 2010
委任: US National Institutes of Health
Coronavirus disease 2019 in patients with inborn errors of immunity: an international study
I Meyts, G Bucciol, I Quinti, B Neven, A Fischer, E Seoane, ...
Journal of Allergy and Clinical Immunology 147 (2), 520-531, 2021
委任: US National Institutes of Health, National Health and Medical Research …
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome
C Woellner, EM Gertz, AA Schäffer, M Lagos, M Perro, EO Glocker, ...
Journal of Allergy and Clinical Immunology 125 (2), 424-432. e8, 2010
委任: US National Institutes of Health, Hungarian Scientific Research Fund
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody …
U Salzer, C Bacchelli, S Buckridge, Q Pan-Hammarström, S Jennings, ...
Blood, The Journal of the American Society of Hematology 113 (9), 1967-1976, 2009
委任: Swiss National Science Foundation, US National Institutes of Health, German …
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