M. Vitali

发表

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

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

A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity

V. Lougaris, A. Plebani, C. Giagulli, 2014, AIDS.

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.

Inhibition of heme synthesis alters Amyloid Precursor Protein processing

P. Arosio, D. Finazzi, R. Verardi, 2008, Journal of Neural Transmission.

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

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

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.

Analysis of the genes coding for subunit 10 and 15 of cytochrome c oxidase in Alzheimer’s disease

D. Galimberti, E. Venturelli, E. Scarpini, 2009, Journal of Neural Transmission.

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.

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.

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

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

BAFF-R mutations in Good's syndrome.

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

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.

Real-time polymerase chain reaction with melting analysis of positive blood culture specimens in bloodstream infections: diagnostic value and turnaround time.

G. Gherardi, S. Galluzzo, S. Angeletti, 2013, The new microbiologica.

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.

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.

Laboratory Automation and Intra-Laboratory Turnaround Time

Silvia Angeletti, Marina De Cesaris, Jonathan George Hart, 2015, Journal of laboratory automation.

Profound T‐cell defects in Dubowitz syndrome

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

Polymorphisms in the LOC387715/ARMS2 Putative Gene and the Risk for Alzheimer’s Disease

D. Galimberti, C. Fenoglio, E. Venturelli, 2008, Dementia and Geriatric Cognitive Disorders.

MALDI-TOF mass spectrometry and blakpc gene phylogenetic analysis of an outbreak of carbapenem-resistant K. pneumoniae strains.

A. Lo Presti, E. Cella, S. Angeletti, 2015, The new microbiologica.

Oral revaccination against poliomyelitis and interference.

G. Nardi, E. Bellelli, M. Vitali, 1966 .

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.