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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 cohort
Francesca 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 deficiency
Vassilios 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 syndrome
Vassilios Lougaris, Manuela Baronio, Massimiliano Vitali, et al.
The Journal of Pediatrics
|
July 22, 2008
Sensorineural hearing loss in primary antibody deficiency disorders
Marco 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 patients
Daniele 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 dysfunction
Pasquale Pignatelli, Roberto Carnevale, Serena Di Santo, et al.
AIDS (London, England)
|
August 15, 2014
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity
Cinzia 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 complications
Domenico 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 4q
Anemone 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 delay
Vassilios Lougaris, Janet Chou, Manuela Baronio, et al.
Page
of 22
Search research articles
Search
Showing results (81-90 of 219) with videos related to
Sort By:
Page
of 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 cohort
Francesca 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 deficiency
Vassilios 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 syndrome
Vassilios Lougaris, Manuela Baronio, Massimiliano Vitali, et al.
The Journal of Pediatrics
|
July 22, 2008
Sensorineural hearing loss in primary antibody deficiency disorders
Marco 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 patients
Daniele 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 dysfunction
Pasquale Pignatelli, Roberto Carnevale, Serena Di Santo, et al.
AIDS (London, England)
|
August 15, 2014
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity
Cinzia 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 complications
Domenico 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 4q
Anemone 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 delay
Vassilios Lougaris, Janet Chou, Manuela Baronio, et al.
Page
of 22