M. Baronio

发表

HIV-1 matrix protein p17 increases the production of proinflammatory cytokines and counteracts IL-4 activity by binding to a cellular receptor

R. Gallo, G. Lewis, E. Garrafa, 2002, Proceedings of the National Academy of Sciences of the United States of America.

HIV-1 p17 binds heparan sulfate proteoglycans to activated CD4(+) T cells.

N. Manca, M. D. De Francesco, M. Baronio, 2008, Virus research.

RAC2 and primary human immune deficiencies

V. Lougaris, A. Plebani, M. Baronio, 2020, Journal of leukocyte biology.

The Genetic Heterogeneity of Common Variable Immunodeficiency (CVID): An Update

Aless, R. Plebani, M. Baronio, 2014 .

A CVID-associated variant in the ciliogenesis protein CCDC28B disrupts immune synapse assembly

V. Lougaris, A. Plebani, M. D’Elios, 2020, Cell Death & Differentiation.

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.

Clinical Study B Cell Responses to CpG Correlate with CXCL 16 Expression Levels in Common Variable Immunodeficiency

V. Lougaris, A. Plebani, R. Badolato, 2014 .

B Cell Responses to CpG Correlate with CXCL16 Expression Levels in Common Variable Immunodeficiency

V. Lougaris, A. Plebani, R. Badolato, 2012, TheScientificWorldJournal.

A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family.

V. Lougaris, A. Plebani, R. Badolato, 2012, Human immunology.

Inhibition of neuroblastoma-induced angiogenesis by fenretinide.

D. Ribatti, A. Vacca, G. Alessandri, 2001, International journal of cancer.

Importance of B cell co‐stimulation in CD4+ T cell differentiation: X‐linked agammaglobulinaemia, a human model

K. Warnatz, B. Grimbacher, M. Perro, 2011, Clinical and experimental immunology.

NFKB1 regulates human NK cell maturation and effector functions.

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

NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential.

V. Lougaris, A. Plebani, C. Cancrini, 2019, Clinical immunology.

Molecular foundations of chiropractic therapy

P. Maltese, S. Michelini, M. Bertelli, 2019, Acta bio-medica : Atenei Parmensis.

Natural small molecules as inhibitors of coronavirus lipid-dependent attachment to host cells: a possible strategy for reducing SARS-COV-2 infectivity?

G. Natalini, T. Beccari, E. Fulcheri, 2020, Acta bio-medica : Atenei Parmensis.

Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation

V. Lougaris, A. Plebani, R. Badolato, 2014, Journal of Clinical Immunology.

Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency.

V. Lougaris, A. Plebani, R. Badolato, 2011, Journal of investigational allergology & clinical immunology.

Clinical and immunological analysis of a large kindred affected by autoimmune lymphoproliferative syndrome (ALPS) due to a novel TNFRSF6 mutation displaying age dependent disease activity.

V. Lougaris, C. Mazza, D. Moratto, 2022, Clinical immunology.

Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS).

V. Lougaris, A. Plebani, R. Badolato, 2021, Clinical immunology.

Polymorphism analysis of Epstein-Barr virus isolates of lymphoblastoid cell lines from patients with mycosis fungoides.

P. Calzavara-Pinton, N. Manca, M. D. De Francesco, 2004, Journal of medical microbiology.

Lymphocyte alterations in patients with Common Variable Immunodeficiency (CVID) and autoimmune manifestations.

V. Lougaris, A. Plebani, R. Badolato, 2022, Clinical immunology.

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.

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

V. Lougaris, A. Plebani, G. Tabellini, 2016, Journal of Allergy and Clinical Immunology.

Human Vasculogenesis Ex Vivo: Embryonal Aorta as a Tool for Isolation of Endothelial Cell Progenitors

E. Parati, G. Alessandri, R. Nicosia, 2001, Laboratory Investigation.

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

V. Lougaris, A. Plebani, R. Badolato, 2017, The Journal of allergy and clinical immunology.

Proteus syndrome: evaluation of the immunological profile

V. Lougaris, A. Plebani, V. Salpietro, 2016, Orphanet Journal of Rare Diseases.

HIV-1 p17 Matrix Protein Interacts with Heparan Sulfate Side Chain of CD44v3, Syndecan-2, and Syndecan-4 Proteoglycans Expressed on Human Activated CD4+ T Cells Affecting Tumor Necrosis Factor α and Interleukin 2 Production*

M. D. De Francesco, M. Baronio, C. Poiesi, 2011, The Journal of Biological Chemistry.

Isolation and culture of human muscle-derived stem cells able to differentiate into myogenic and neurogenic cell lineages

G. Invernici, E. Parati, G. Alessandri, 2004, The Lancet.

The nested graft acts by inducing the process of de‐senescence of the fibroblasts in chronic venous ulcers

V. Lougaris, P. Calzavara-Pinton, G. Gualdi, 2016, International wound journal.

Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay.

V. Lougaris, A. Plebani, R. Badolato, 2017, Clinical immunology.

Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype.

V. Lougaris, A. Plebani, S. Giliani, 2015, Clinical immunology.

From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies

L. Notarangelo, V. Lougaris, A. Plebani, 2019, Front. Immunol..

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

Bodo Grimbacher, Alejandro A Schäffer, Giacomo Tampella, 2012, American journal of human genetics.

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.

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.

Etiopathogenesis of sacroiliitis: implications for assessment and management

G. Natalini, M. Bertelli, H. Sadia, 2020, The Korean journal of pain.

Molecular Aspects of Regional Pain Syndrome

G. Natalini, M. Bertelli, H. Sadia, 2020, Pain research & management.

Inhibition of neuroblastoma‐induced angiogenesis by fenretinide

D. Ribatti, A. Vacca, G. Alessandri, 2001 .

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.

Remitting symmetric seronegative synovitis with pitting edema associated with B-cell non-Hodgkin's lymphoma.

C. Cappelli, P. Airó, M. Baronio, 2000, Clinical and experimental rheumatology.

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.

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.

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.

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.

Thromboprophylaxis with enoxaparin is associated with a lower death rate in patients hospitalized with SARS-CoV-2 infection. A cohort study

M. Massari, G. Natalini, M. E. Franceschetti, 2020, EClinicalMedicine.

Myeloid microvesicles in cerebrospinal fluid are associated with myelin damage and neuronal loss in mild cognitive impairment and Alzheimer disease

F. Agosta, G. Comi, G. Magnani, 2014, Annals of neurology.

Cerebrospinal fluid markers for Alzheimer's disease in a cognitively healthy cohort of young and old adults

G. Frisoni, S. Galluzzi, G. Amicucci, 2012, Alzheimer's & Dementia.

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.

Italian SARS-CoV-2 patients in intensive care: towards an identikit for subjects at risk?

G. Natalini, M. Pinelli, P. Chiurazzi, 2020, European review for medical and pharmacological sciences.

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

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

Automatic and manual devices for cardiopulmonary resuscitation: A review

Nicola Pellegrini, Riccardo Adamini, Francesco Aggogeri, 2018 .

Ventricular defibrillation: Classification with G.E.M. and a roadmap for future investigations

Fabio Baronio, Marco C. Campi, Simone Garatti, 2017, 2017 IEEE 56th Annual Conference on Decision and Control (CDC).

CTLA-4 regulates human Natural Killer cell effector functions.

V. Lougaris, A. Plebani, G. Tabellini, 2018, Clinical immunology.

Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation

V. Lougaris, A. Plebani, R. Badolato, 2014, Journal of Clinical Immunology.

The RAC2-PI3K axis regulates human NK cell maturation and function.

V. Lougaris, A. Plebani, G. Tabellini, 2019, Clinical immunology.

Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations

M. Chiarini, V. Lougaris, A. Plebani, 2021, Journal of Clinical Immunology.

Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations

V. Lougaris, A. Plebani, R. Badolato, 2021, Journal of Clinical Immunology.

Profound T‐cell defects in Dubowitz syndrome

V. Lougaris, A. Plebani, P. Calzavara-Pinton, 2014, Pediatric Allergy and Immunology.

Lack of DOCK8 impairs the primary biologic functions of human NK cells and abrogates CCR7 surface expression in a WASP-independent manner.

V. Lougaris, A. Plebani, R. Badolato, 2022, Clinical immunology.

Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity.

V. Lougaris, A. Plebani, D. Moratto, 2019, Clinical immunology.

A CVID-associated variant in the ciliogenesis protein CCDC28B disrupts immune synapse assembly

V. Lougaris, A. Plebani, M. D’Elios, 2021, Cell Death & Differentiation.

CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis.

V. Lougaris, R. Badolato, G. Tabellini, 2023, Immunobiology.

Clinical and morphological features of kidney involvement in primary Sjögren's syndrome.

F. Scolari, B. F. Viola, S. Savoldi, 2001, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Genetic and physiological autonomic nervous system factors involved in failed back surgery syndrome: A review of the literature and report of nine cases treated with pulsed radiofrequency

G. Natalini, P. Notaro, M. Baglivo, 2020, Acta bio-medica : Atenei Parmensis.

Reduced germinal center follicular helper T cells but normal follicular regulatory T cells in the tonsils of a patient with a mutation in the PI3KR1 gene.

V. Lougaris, A. Plebani, G. Fousteri, 2016, Clinical immunology.

Myeloid microvesicles in cerebrospinal fluid are associated with myelin damage and neuronal loss in mild cognitive impairment and Alzheimer disease

F. Agosta, G. Comi, G. Magnani, 2014, Annals of neurology.

Cardiopulmonary Resuscitation Devices: Preliminary Analysis

Alberto Borboni, Nicola Pellegrini, Riccardo Adamini, 2017, RAAD.

A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy.

V. Lougaris, A. Plebani, V. Villanacci, 2018, Clinical immunology.

Fatal SARS-CoV-2 infection in a male patient with Good's syndrome

M. Chiarini, V. Lougaris, A. Plebani, 2020, Clinical Immunology.

Monogenic forms of common variable immunodeficiency and implications on target therapeutic approaches

V. Lougaris, M. Baronio, G. Tessarin, 2023, Current opinion in allergy and clinical immunology.

Patients with STAT1 Gain-of-function Mutations Display Increased Apoptosis which is Reversed by the JAK Inhibitor Ruxolitinib

L. Dotta, S. Giliani, D. Moratto, 2024, Journal of clinical immunology.

Potential therapeutic role of pharmacological sympathectomy in Martorell ulcer

R. De Gaudio, S. Romagnoli, M. Baglivo, 2021, Postepy dermatologii i alergologii.

Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations

V. Lougaris, F. Chiarelli, G. Lombardi, 2014, Journal of Clinical Immunology.

Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome.

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