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Alessandro Plebani

Showing results (131-140 of 219) with videos related to

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Clinical Immunology (Orlando, Fla.)|January 7, 2016
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung diseaseLaura Dotta, Omar Scomodon, Rita Padoan, et al.
Data in Brief|March 17, 2016
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis diseaseLaura Dotta, Omar Scomodon, Rita Padoan, et al.
Cell|January 28, 2006
Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephalyDietke Buck, Laurent Malivert, Régina de Chasseval, et al.
Journal of the American Heart Association|June 29, 2014
Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous diseaseRoberto Carnevale, Lorenzo Loffredo, Valerio Sanguigni, et al.
The Journal of Allergy and Clinical Immunology|January 11, 2017
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutationsGiovanna Tabellini, Donatella Vairo, Omar Scomodon, et al.
The Journal of Allergy and Clinical Immunology|January 18, 2019
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiencyVassilios Lougaris, Janet Chou, Abdallah Beano, et al.
Clinical Immunology (Orlando, Fla.)|April 20, 2004
Search for poliovirus long-term excretors among patients affected by agammaglobulinemiaLucia Fiore, Alessandro Plebani, Gabriele Buttinelli, et al.
The Journal of Allergy and Clinical Immunology. in Practice|February 24, 2019
Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgETiziana Lorenzini, Mauro Giacomelli, Omar Scomodon, et al.
International Archives of Allergy and Immunology|September 1, 2006
Clinical, immunological and molecular characteristics of 37 Iranian patients with X-linked agammaglobulinemiaAsghar Aghamohammadi, Maurilia Fiorini, Mostafa Moin, et al.
Circulation|October 7, 2009
Hereditary deficiency of gp91(phox) is associated with enhanced arterial dilatation: results of a multicenter studyFrancesco Violi, Valerio Sanguigni, Roberto Carnevale, et al.
Pageof 22

Showing results (131-140 of 219) with videos related to

Sort By:
Pageof 22
Clinical Immunology (Orlando, Fla.)|January 7, 2016
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung diseaseLaura Dotta, Omar Scomodon, Rita Padoan, et al.
Data in Brief|March 17, 2016
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis diseaseLaura Dotta, Omar Scomodon, Rita Padoan, et al.
Cell|January 28, 2006
Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephalyDietke Buck, Laurent Malivert, Régina de Chasseval, et al.
Journal of the American Heart Association|June 29, 2014
Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous diseaseRoberto Carnevale, Lorenzo Loffredo, Valerio Sanguigni, et al.
The Journal of Allergy and Clinical Immunology|January 11, 2017
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutationsGiovanna Tabellini, Donatella Vairo, Omar Scomodon, et al.
The Journal of Allergy and Clinical Immunology|January 18, 2019
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiencyVassilios Lougaris, Janet Chou, Abdallah Beano, et al.
Clinical Immunology (Orlando, Fla.)|April 20, 2004
Search for poliovirus long-term excretors among patients affected by agammaglobulinemiaLucia Fiore, Alessandro Plebani, Gabriele Buttinelli, et al.
The Journal of Allergy and Clinical Immunology. in Practice|February 24, 2019
Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgETiziana Lorenzini, Mauro Giacomelli, Omar Scomodon, et al.
International Archives of Allergy and Immunology|September 1, 2006
Clinical, immunological and molecular characteristics of 37 Iranian patients with X-linked agammaglobulinemiaAsghar Aghamohammadi, Maurilia Fiorini, Mostafa Moin, et al.
Circulation|October 7, 2009
Hereditary deficiency of gp91(phox) is associated with enhanced arterial dilatation: results of a multicenter studyFrancesco Violi, Valerio Sanguigni, Roberto Carnevale, et al.
Pageof 22