V. Lougaris

V. Lougaris, A. Plebani, A. Durandy, 2021, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Allergen immunotherapy, routes of administration and cytokine networks: an update.

V. Lougaris, S. Manti, S. Leonardi, 2014, Immunotherapy.

Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor 𝛋B kinase alpha (IKKα)

V. Lougaris, A. Plebani, R. Hoyos-Bachiloglu, 2021, Science Immunology.

Agammaglobulinemias: Basic Pathogenesis and Clinical Spectrum

V. Lougaris, A. Plebani, 2015 .

Autosomal Recessive Agammaglobulinemia: A Novel Non-sense Mutation in CD79a

V. Lougaris, A. Plebani, N. Rezaei, 2014, Journal of Clinical Immunology.

Mutations of the Igβ gene cause agammaglobulinemia in man

V. Lougaris, A. Plebani, M. Reth, 2007, The Journal of experimental medicine.

Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia

V. Lougaris, A. Plebani, F. Cardinale, 2007, Genes and Immunity.

Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content

L. Notarangelo, J. Walter, V. Lougaris, 2017, Front. Immunol..

Modeling, optimization, and comparable efficacy of T cell and hematopoietic stem cell gene editing for treating hyper‐IgM syndrome

V. Lougaris, A. Plebani, P. Rancoita, 2021, EMBO molecular medicine.

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

V. Lougaris, A. Plebani, D. Moratto, 2016, Clinical immunology.

Correction: Corrigendum: B cell–helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen

S. Serrano, J. Lloreta, J. Casanova, 2014, Nature Immunology.

The Interplay between CD27dull and CD27bright B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory.

A. N. Davydov, V. Lougaris, A. Plebani, 2020, Cell reports.

1-1-2016 Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing

Alessandro, E. Farrow, C. Saunders, 2019 .

Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data

V. Lougaris, L. Mascaro, R. Maroldi, 2014, La radiologia medica.

Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations.

V. Lougaris, R. Badolato, S. Giliani, 2020, Clinical immunology.

A possible role for B cells in COVID-19? Lesson from patients with agammaglobulinemia

V. Lougaris, A. Plebani, O. Turriziani, 2020, Journal of Allergy and Clinical Immunology.

Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) in Common Variable Immunodeficiency (CVID): A Multicenter Retrospective Study of Patients From Italian PID Referral Centers

V. Lougaris, A. Plebani, D. Consonni, 2021, Frontiers in Immunology.

Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients

V. Lougaris, R. Badolato, R. Kosaki, 2020, Journal of Clinical Immunology.

Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network

G. Giardino, E. Cirillo, V. Lougaris, 2019, Front. Immunol..

Maternal T-cell engraftment impedes with diagnosis of a SCID-ADA patient

V. Lougaris, L. Notarangelo, L. Imberti, 2018, Clinical Immunology.

Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies

V. Lougaris, A. Plebani, F. Cardinale, 2015, Journal of Clinical Immunology.

BAFF-R mutations in Good's syndrome.

V. Lougaris, A. Plebani, M. Baronio, 2014, Clinical immunology.

The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019)

V. Lougaris, R. Consolini, A. Plebani, 2020, Journal of Clinical Immunology.

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

V. Lougaris, A. Plebani, B. Grimbacher, 2019, Clinical immunology.

Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study

V. Lougaris, A. Plebani, R. Badolato, 2019, Journal of Clinical Immunology.

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

V. Lougaris, A. Plebani, G. Gualdi, 2015, Journal of investigational allergology & clinical immunology.

A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency.

V. Lougaris, A. Plebani, Michael Seleman, 2019, The Journal of allergy and clinical immunology.

Mutational Analysis of Human BLyS in Patients with Common Variable Immunodeficiency

V. Lougaris, A. Plebani, B. Grimbacher, 2006, Journal of Clinical Immunology.

Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality.

E. Cirillo, V. Lougaris, R. Consolini, 2020, The Journal of allergy and clinical immunology.

Sensorineural hearing loss in primary antibody deficiency disorders.

V. Lougaris, A. Plebani, P. Nicolai, 2008, The Journal of pediatrics.

Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents.

J. Casanova, V. Lougaris, A. Plebani, 2021, The Journal of clinical investigation.

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

V. Lougaris, A. Plebani, G. Tabellini, 2015, The Journal of allergy and clinical immunology.

Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease

L. Dotta, G. Giardino, V. Lougaris, 2016, Data in brief.

Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications.

V. Lougaris, A. Plebani, R. Badolato, 2018, Clinical immunology.

Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion.

V. Lougaris, A. Plebani, D. Russo, 2020, Clinical immunology.

Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis.

Anne-Kathrin Kienzler, V. Lougaris, A. Plebani, 2014, The Journal of allergy and clinical immunology.

Inherited defects in the complement system

G. Giardino, V. Lougaris, C. Cancrini, 2022, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Consensus of the Italian Primary Immunodeficiency Network on Transition Management from Pediatric to Adult Care in Patients Affected with Childhood Onset Inborn Errors of Immunity.

L. Dotta, G. Giardino, E. Cirillo, 2020, The Journal of allergy and clinical immunology.

The significance of duodenal mucosal atrophy in patients with common variable immunodeficiency: a clinical and histopathologic study.

V. Lougaris, A. Plebani, G. Corazza, 2012, American journal of clinical pathology.

Paediatric MAS/HLH caused by a novel monoallelic activating mutation in p110δ.

V. Lougaris, A. Plebani, R. Badolato, 2020, Clinical immunology.

Circulating Follicular Helper and Follicular Regulatory T Cells Are Severely Compromised in Human CD40 Deficiency: A Case Report

V. Lougaris, A. Plebani, A. Aiuti, 2018, Front. Immunol..

Beta2 integrins are required for follicular helper T cell differentiation in humans.

V. Lougaris, A. Plebani, G. Fousteri, 2017, Clinical immunology.

Immune tolerance breakdown in inborn errors of immunity: Paving the way to novel therapeutic approaches.

G. Giardino, V. Lougaris, C. Pignata, 2023, Clinical immunology.

Clinical and immunologic phenotype associated with activated ă phosphoinositide 3-kinase delta syndrome 2: A cohort study

T. Molina, A. Fischer, S. Nejentsev, 2016 .

Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects

V. Lougaris, A. Plebani, S. Giliani, 2016, Expert review of clinical immunology.

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

V. Lougaris, A. Plebani, R. Badolato, 2014, The Journal of allergy and clinical immunology.

E47 Transcription Factor Deficiency

V. Lougaris, A. Plebani, 2020, Encyclopedia of Medical Immunology.

Serum Immunoglobulin Isotypes with Decreased or Absent B Cells, Reduction of