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Alessandro Plebani

Showing results (81-90 of 219) with videos related to

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Clinical Immunology (Orlando, Fla.)|February 18, 2021
Temporal viral loads in respiratory and gastrointestinal tract and serum antibody responses during SARS-CoV-2 infection in an Italian pediatric cohortFrancesca Caccuri, Antonella Bugatti, Antonella Meini, et al.
Clinical Immunology (Orlando, Fla.)|February 25, 2018
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiencyVassilios Lougaris, Gaetana Lanzi, Manuela Baronio, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|June 6, 2014
Profound T-cell defects in Dubowitz syndromeVassilios Lougaris, Manuela Baronio, Massimiliano Vitali, et al.
The Journal of Pediatrics|July 22, 2008
Sensorineural hearing loss in primary antibody deficiency disordersMarco Berlucchi, Annarosa Soresina, Luca O Redaelli De Zinis, et al.
Clinical Immunology (Orlando, Fla.)|September 12, 2006
Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patientsDaniele Moratto, Anna Virginia Gulino, Stefania Fontana, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 13, 2010
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunctionPasquale Pignatelli, Roberto Carnevale, Serena Di Santo, et al.
AIDS (London, England)|August 15, 2014
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activityCinzia Giagulli, Francesca Caccuri, Francesca Cignarella, et al.
Clinical Immunology (Orlando, Fla.)|March 18, 2018
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complicationsDomenico Umberto De Rose, Silvia Giliani, Lucia Dora Notarangelo, et al.
European Journal of Human Genetics : EJHG|April 28, 2006
Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4qAnemone Finck, Jos W M Van der Meer, Alejandro A Schäffer, et al.
Clinical Immunology (Orlando, Fla.)|November 25, 2017
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delayVassilios Lougaris, Janet Chou, Manuela Baronio, et al.
Pageof 22

Showing results (81-90 of 219) with videos related to

Sort By:
Pageof 22
Clinical Immunology (Orlando, Fla.)|February 18, 2021
Temporal viral loads in respiratory and gastrointestinal tract and serum antibody responses during SARS-CoV-2 infection in an Italian pediatric cohortFrancesca Caccuri, Antonella Bugatti, Antonella Meini, et al.
Clinical Immunology (Orlando, Fla.)|February 25, 2018
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiencyVassilios Lougaris, Gaetana Lanzi, Manuela Baronio, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|June 6, 2014
Profound T-cell defects in Dubowitz syndromeVassilios Lougaris, Manuela Baronio, Massimiliano Vitali, et al.
The Journal of Pediatrics|July 22, 2008
Sensorineural hearing loss in primary antibody deficiency disordersMarco Berlucchi, Annarosa Soresina, Luca O Redaelli De Zinis, et al.
Clinical Immunology (Orlando, Fla.)|September 12, 2006
Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patientsDaniele Moratto, Anna Virginia Gulino, Stefania Fontana, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 13, 2010
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunctionPasquale Pignatelli, Roberto Carnevale, Serena Di Santo, et al.
AIDS (London, England)|August 15, 2014
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activityCinzia Giagulli, Francesca Caccuri, Francesca Cignarella, et al.
Clinical Immunology (Orlando, Fla.)|March 18, 2018
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complicationsDomenico Umberto De Rose, Silvia Giliani, Lucia Dora Notarangelo, et al.
European Journal of Human Genetics : EJHG|April 28, 2006
Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4qAnemone Finck, Jos W M Van der Meer, Alejandro A Schäffer, et al.
Clinical Immunology (Orlando, Fla.)|November 25, 2017
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delayVassilios Lougaris, Janet Chou, Manuela Baronio, et al.
Pageof 22