Giacomo Tampella

Brescia, Italy

Last Updated: 09/26/2026

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Found 13 publications

A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1).

A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1).

Journal: Clinical immunology (Orlando, Fla.)

Published: November 16, 2018

NFKB1 regulates human NK cell maturation and effector functions.

NFKB1 regulates human NK cell maturation and effector functions.

Journal: Clinical immunology (Orlando, Fla.)

Published: July 08, 2016

Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease.

Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease.

Journal: The Journal of allergy and clinical immunology

Published: February 24, 2016

Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency.

Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency.

Journal: Journal of investigational allergology & clinical immunology

Published: January 06, 2016

Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients.

Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients.

Journal: Clinical immunology (Orlando, Fla.)

Published: November 16, 2015

p85α is an intrinsic regulator of human natural killer cell effector functions.

p85α is an intrinsic regulator of human natural killer cell effector functions.

Journal: The Journal of allergy and clinical immunology

Published: September 03, 2015

Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease.

Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease.

Journal: The Journal of allergy and clinical immunology

Published: September 16, 2014

Profound T-cell defects in Dubowitz syndrome.

Profound T-cell defects in Dubowitz syndrome.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: June 06, 2014

BAFF-R mutations in Good's syndrome.

BAFF-R mutations in Good's syndrome.

Journal: Clinical immunology (Orlando, Fla.)

Published: April 02, 2014

Autosomal recessive agammaglobulinemia: the third case of Igβ deficiency due to a novel non-sense mutation.

Autosomal recessive agammaglobulinemia: the third case of Igβ deficiency due to a novel non-sense mutation.

Journal: Journal of clinical immunology

Published: February 13, 2014

Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation.

Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation.

Journal: The Journal of allergy and clinical immunology

Published: July 04, 2013

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.

Journal: American journal of human genetics

Published: January 19, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026