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Raffaele Badolato

Showing results (41-50 of 183) with videos related to

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British Journal of Haematology|January 18, 2021
More than an 'atypical' phenotype: dual molecular diagnosis of autoimmune lymphoproliferative syndrome and Becker muscular dystrophyFrancesco Saettini, Vincenzo L'Imperio, Grazia Fazio, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|March 15, 2008
Decreased type I interferon receptor-soluble isoform in antiretroviral-treated HIV-positive childrenAlessandra Sottini, Claudia Ghidini, Federico Serana, et al.
The Journal of Allergy and Clinical Immunology|March 12, 2014
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activationVassilios Lougaris, Manuela Baronio, Massimiliano Vitali, et al.
Italian Journal of Pediatrics|February 4, 2022
Incidence of acute respiratory infections in preschool children in an outpatient setting before and during Covid-19 pandemic in Lombardy Region, ItalyChiara Mameli, Marina Picca, Roberto Buzzetti, et al.
Orphanet Journal of Rare Diseases|March 2, 2019
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: neuroimaging and clinical findingsJessica Galli, Lorenzo Pinelli, Serena Micheletti, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|June 1, 2019
The hidden hypothesis: A disseminated tuberculosis caseSergio Foresti, Maria Rita Perego, Manuela Carugati, et al.
Clinical Case Reports|August 3, 2023
Treatment response to Janus kinase inhibitor in a child affected by Aicardi-Goutières syndromeJessica Galli, Marco Cattalini, Erika Loi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 25, 2009
Uncovering an IL-10-dependent NF-kappaB recruitment to the IL-1ra promoter that is impaired in STAT3 functionally defective patientsNicola Tamassia, Monica Castellucci, Marzia Rossato, et al.
Clinical Immunology (Orlando, Fla.)|July 17, 2022
Lymphocyte alterations in patients with Common Variable Immunodeficiency (CVID) and autoimmune manifestationsStefano Rossi, Manuela Baronio, Luisa Gazzurelli, et al.
European Journal of Immunology|July 28, 2011
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 functionMauro Giacomelli, Nicola Tamassia, Daniele Moratto, et al.
Pageof 19

Showing results (41-50 of 183) with videos related to

Sort By:
Pageof 19
British Journal of Haematology|January 18, 2021
More than an 'atypical' phenotype: dual molecular diagnosis of autoimmune lymphoproliferative syndrome and Becker muscular dystrophyFrancesco Saettini, Vincenzo L'Imperio, Grazia Fazio, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|March 15, 2008
Decreased type I interferon receptor-soluble isoform in antiretroviral-treated HIV-positive childrenAlessandra Sottini, Claudia Ghidini, Federico Serana, et al.
The Journal of Allergy and Clinical Immunology|March 12, 2014
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activationVassilios Lougaris, Manuela Baronio, Massimiliano Vitali, et al.
Italian Journal of Pediatrics|February 4, 2022
Incidence of acute respiratory infections in preschool children in an outpatient setting before and during Covid-19 pandemic in Lombardy Region, ItalyChiara Mameli, Marina Picca, Roberto Buzzetti, et al.
Orphanet Journal of Rare Diseases|March 2, 2019
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: neuroimaging and clinical findingsJessica Galli, Lorenzo Pinelli, Serena Micheletti, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|June 1, 2019
The hidden hypothesis: A disseminated tuberculosis caseSergio Foresti, Maria Rita Perego, Manuela Carugati, et al.
Clinical Case Reports|August 3, 2023
Treatment response to Janus kinase inhibitor in a child affected by Aicardi-Goutières syndromeJessica Galli, Marco Cattalini, Erika Loi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 25, 2009
Uncovering an IL-10-dependent NF-kappaB recruitment to the IL-1ra promoter that is impaired in STAT3 functionally defective patientsNicola Tamassia, Monica Castellucci, Marzia Rossato, et al.
Clinical Immunology (Orlando, Fla.)|July 17, 2022
Lymphocyte alterations in patients with Common Variable Immunodeficiency (CVID) and autoimmune manifestationsStefano Rossi, Manuela Baronio, Luisa Gazzurelli, et al.
European Journal of Immunology|July 28, 2011
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 functionMauro Giacomelli, Nicola Tamassia, Daniele Moratto, et al.
Pageof 19