Detalhe da pesquisa
1.
Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.
J Allergy Clin Immunol;
152(4): 984-996.e10, 2023 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37390899
2.
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
J Allergy Clin Immunol;
146(4): 901-911, 2020 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32278790
3.
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity.
Clin Immunol;
205: 153-155, 2019 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30500415
4.
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study.
J Clin Immunol;
39(5): 470-475, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31129864
5.
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography.
J Clin Immunol;
37(1): 36-41, 2017 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27766541
6.
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions.
J Allergy Clin Immunol;
138(1): 229-240.e3, 2016 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26875746
7.
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients.
Clin Immunol;
163: 10-3, 2016 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26686461
8.
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency.
J Allergy Clin Immunol;
143(4): 1649-1653.e3, 2019 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30654050
9.
Alterations of Thymus-Derived Tregs in Multiple Sclerosis.
Neurol Neuroimmunol Neuroinflamm;
11(4): e200251, 2024 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38838284
10.
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency.
Clin Immunol;
190: 11-14, 2018 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29476811
11.
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy.
Clin Immunol;
197: 186-188, 2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30326257
12.
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay.
Clin Immunol;
188: 20-22, 2018 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29170023
13.
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome.
Clin Immunol;
173: 181-183, 2016 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27825976
14.
Severe T-cell lymphopenia in a patient with microduplication 22q11.2 identified by newborn screening.
J Allergy Clin Immunol Pract;
2024 May 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38729303
15.
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET).
Vaccine;
36(24): 3541-3554, 2018 06 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29426658
16.
STAT mutations as program switchers: turning primary immunodeficiencies into autoimmune diseases.
J Leukoc Biol;
101(1): 29-38, 2017 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27803128
17.
Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE.
J Allergy Clin Immunol Pract;
7(6): 2072-2075.e4, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30797078
18.
Corrigendum to: "Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET)" [Vaccine 36 (2018) Pages 3541-3542].
Vaccine;
36(50): 7753, 2018 11 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30389193