B. Martire

C. Rizzo, D. Montin, L. Chini, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Hereditary Deficiency of gp91 phox Is Associated With Enhanced Arterial Dilatation Results of a Multicenter Study

A. Plebani, C. Pignata, E. Gambineri, 2009 .

Search for poliovirus long-term excretors among patients affected by agammaglobulinemia.

A. Plebani, C. Pignata, A. Ugazio, 2004, Clinical immunology.

Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study.

L. Notarangelo, R. Consolini, A. Plebani, 2002, Clinical immunology.

Reduced Interleukin-5 Production by Peripheral Cd4+ T Cells in Common Variable Immunodeficiency Patients

P. Giordano, G. Lassandro, G. C. Del Vecchio, 2008 .

Does NADPH oxidase deficiency cause artery dilatation in humans?

G. Giardino, A. Plebani, C. Pignata, 2013, Antioxidants & redox signaling.

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

G. Scarano, V. Gallo, G. Giardino, 2014, BMC Medical Genetics.

Effectiveness of thymostimulin and study of lymphocyte-dependent antibacterial activity in children with recurrent respiratory infections.

P. Ferrante, E. Jirillo, F. Schettini, 1993, Immunopharmacology and immunotoxicology.

Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients

M. Chiarini, V. Lougaris, A. Plebani, 2020, Journal of clinical medicine.

Congenital and acquired neutropenias consensus guidelines on therapy and follow‐up in childhood from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato‐Oncologia Pediatrica)

E. Gambineri, M. Pillon, G. Menna, 2012, American journal of hematology.

E. Cirillo, A. Plebani, C. Pignata, 2019, Journal of Clinical Immunology.

Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: an Italian multicenter study.

A. Plebani, C. Pignata, M. Chiriacò, 2009, Molecular immunology.

Initial presenting manifestations in 16,486 patients with Inborn Errors of Immunity include infections and non-infectious manifestations.

Nurit Assia Batzir, K. Schwarz, D. Foell, 2021, The Journal of allergy and clinical immunology.

Erythema infectiosum following generalized petechial eruption induced by human parvovirus B19.

C. Foti, D. Bonamonte, C. Casulli, 2006, The new microbiologica.

Pulmonary and sinus diseases in primary humoral immunodeficiencies with chronic productive cough

F. Rusconi, F. Cardinale, F. Cardinale, 2003, Archives of disease in childhood.

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.

Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization.

L. Notarangelo, S. Giliani, F. Candotti, 2000, Clinical immunology.

Congenital and acquired neutropenia consensus guidelines on diagnosis from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato‐Oncologia Pediatrica)

Daniela Renga, M. Pillon, G. Menna, 2011, Pediatric blood & cancer.

Clinical features and follow-up in patients with 22q11.2 deletion syndrome.

E. Cirillo, R. Consolini, A. Plebani, 2014, The Journal of pediatrics.

Lethal sepsis and malignant transformation in severe congenital neutropenia: Report from the Italian Neutropenia Registry

F. Cardinale, M. Calvillo, C. Dufour, 2015, Pediatric blood & cancer.

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..

Transfusion‐dependent congenital dyserythropoietic anaemia with intraerythroblastic inclusionsof a non‐globin protein

A. Iolascon, S. Wickramasinghe, B. Martire, 2000, European journal of haematology.

Biweekly Hizentra® in Primary Immunodeficiency: a Multicenter, Observational Cohort Study (IBIS)

V. Gallo, C. Pignata, A. Matucci, 2018, Journal of Clinical Immunology.

Shift from intravenous or 16% subcutaneous replacement therapy to 20% subcutaneous immunoglobulin in patients with primary antibody deficiencies

A. Plebani, F. Cinetto, M. de Carli, 2016, International journal of immunopathology and pharmacology.

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.

Autoimmune haematological disorders in two Italian children with Kabuki Syndrome

P. Giordano, G. Lassandro, M. Faienza, 2014, Italian Journal of Pediatrics.

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.

Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome.

G. Giardino, R. Consolini, A. Plebani, 2019, The journal of allergy and clinical immunology. In practice.

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.

Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies.

V. Lougaris, A. Plebani, F. Cinetto, 2019, The Journal of allergy and clinical immunology.

Anti-infective prophylaxis for primary immunodeficiencies: what is done in Italian Primary Immunodeficiency Network centers (IPINet) and review of the literature.

C. Pignata, C. Cancrini, A. Ugazio, 2013, Journal of biological regulators and homeostatic agents.

Pediatric subset of primary immunodeficiency patients treated with SCIG: post hoc analysis of SHIFT and IBIS pooled data

C. Canessa, V. Moschese, B. Martire, 2020, Allergy, Asthma & Clinical Immunology.

Subcutaneous Immunoglobulin Twenty Percent Every Two Weeks in Pediatric Patients with Primary Immunodeficiencies: Subcohort Analysis of the IBIS Study.

V. Gallo, C. Pignata, A. Matucci, 2019, Pediatric allergy, immunology, and pulmonology.

Biweekly Hizentra® in Primary Immunodeficiency: a Multicenter, Observational Cohort Study (IBIS)

V. Gallo, C. Pignata, A. Matucci, 2018, Journal of Clinical Immunology.

Persistent B‐cell Lymphopenia, Multiorgan Disease, and Erythema Multiforme Caused by Mycoplasma pneumoniae Infection

C. Foti, N. Cassano, R. Buquicchio, 2005, Pediatric dermatology.

Successful Treatment with Cyclosporine A of HCV-Driven Chronic Liver Disease Mimicking Autoimmune Hepatitis in a Patient with Common Variable Immunodeficiency

R. Francavilla, D. De Mattia, B. Martire, 2005, Immunopharmacology and immunotoxicology.

Diagnosis and management of urinary tract infections in children aged 2 months to 3 years in the Italian emergency units: the ItaUTI study

E. Palumbo, G. Marseglia, I. Rabbone, 2022, European Journal of Pediatrics.

Hospitalization for bronchiolitis in children aged ≤ 1year, Southern Italy, year 2021: need for new preventive strategies?

F. Centrone, N. Laforgia, M. Chironna, 2023, Italian Journal of Pediatrics.

Hepatic non-Hodgkin lymphoma and hepatoblastoma complicating ataxia-telangiectasia

N. Santoro, G. Arcamone, V. Cecinati, 2012, Immunopharmacology and immunotoxicology.

Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived From Structural and Functional Analysis of 14 ClC‐7 Mutants

G. Baynam, A. Kariminejad, A. Rehman, 2020, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Novel artful applications of vaccines at the horizon

C. Rizzo, D. Montin, L. Chini, 2022, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

CHARGE syndrome and common variable immunodeficiency: A case report and review of literature

R. Panza, M. Pillon, M. Delvecchio, 2016, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Growth hormone deficiency and antipituitary antibodies in a patient with common variable immunodeficiency

A. Bellis, M. Delvecchio, D. Mattia, 2009, Journal of endocrinological investigation.

Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived from Structural and Functional Analysis of 14 ClC-7 Mutants. Journal of Bone and Mineral Research.

A. Picollo, L. Lagostena, R. Chiesa, 2020 .