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JOURNAL OF CLINICAL IMMUNOLOGY
Rivista
Codice:
E091033
ISSN:
0271-9142
Dati Generali
Dati Generali
Pubblicazioni (45)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association
Articolo
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID)
Abstract
ARTEMIS AND LIGASE 4 ARE DISPENSABLE FOR THE GENERATION OF HUMAN INDUCED PLURIPOTENT STEM CELLS
Abstract
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity
Abstract
Alternative Approach to Varicella Zoster Virus Prevention in a Child with Lymphopenia
Articolo
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation.
Articolo
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a.
Articolo
CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES
Abstract
CHARACTERIZATION OF AUTOANTIBODY PROFILE AMONG PATIENTS WITH PRIMARY IMMUNODEFICIENCY SECONDARY TO RAG MUTATION
Abstract
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study
Articolo
DISCRIMINATION AMONG MONOGENIC AND ACQUIRED DISEASE WITH INFLAMMATORY AND AUTOIMMUNE COMPONENT THROUGH THE IN VITRO STUDY OF SIGNAL TRANSDUCERS OF TYPE I INTERFERON
Abstract
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography
Articolo
Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study.
Articolo
Exome Sequencing Reveals a Pallidin Mutation in a Hermansky-Pudlak-Like Primary Immunodeficiency Syndrome
Abstract
Exploring Autoimmunity in a Cohort of Children with Genetically Confirmed Aicardi–Goutières Syndrome
Articolo
Flow Cytometry Identifies Risk Factors and Dynamic Changes in Patients with COVID-19
Articolo
GENETIC ANALYSIS OF THE TNFRSF13B GENE IN A LARGE ITALIAN CVID COHORT
Abstract
HAPLOIDENTICAL TCR-ALPHA/BETA AND CD19-DEPLETED HEMATOPOIETIC STEM CELL TRANSPLANTATION IN A CASE OF SCID
Abstract
IMMUNODEFICIENCY, AUTO-INFLAMMATION AND MUSCULAR AMYLOPECTINOSIS IN PATIENTS MISSING AN UBIQUITIN LIGASE
Abstract
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group
Articolo
Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations
Articolo
Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency
Articolo
Long-term follow-up and outcome of a large cohort of patients with common variable immunodeficiency.
Articolo
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies
Articolo
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency.
Articolo
Mutational analysis of human BLyS in patients with common variable immunodeficiency.
Articolo
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study
Articolo
PROSPECTIVE STUDY OF 84 PATIENTS WITH WISKOTT-ALDRICH SYNDROME AND X-RECESSIVE PIASTRINOPENIA: RESULTS OF THE APPLICATION OF COMMON PROTOCOL FOR DIAGNOSIS AND TREATMENT OF WAS/XLT
Abstract
Patients with STAT1 Gain-of-function Mutations Display Increased Apoptosis which is Reversed by the JAK Inhibitor Ruxolitinib
Articolo
Prevalence and clinical correlations of antibodies against six beta2-glycoprotein-I-related peptides in the antiphospholipid syndrome.
Articolo
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients
Articolo
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network
Articolo
Prospective study on CVID patients with adverse reactions to intravenous or subcutaneous IgG administration.
Articolo
Response to the Letter to the Editor Regarding âKinetics of Radiological Response of Thoracic Invasive Fungal Disease in Chronic Granulomatous Diseaseâ
Articolo
Rituximab Monotherapy Is Effective as First-Line Treatment for Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) in CVID Patients
Articolo
SP110 REGULATES NUCLEAR ORPHAN RECEPTOR NUR77-DRIVEN APOPTOSIS IN T CELLS
Abstract
Severe Combined Immunodeficiency in Greek Children over a 20-Year Period : Rarity of g(c)-Chain Deficiency (X-Linked) Type
Articolo
Severe combined immunodeficiency in Serbia and Montenegro between years 1986 and 2010: a single-center experience.
Articolo
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations
Articolo
Successful Hematopoietic Stem Cell Transplantation in a Patient with Complete IFN-γ Receptor 2 Deficiency: a Case Report and Literature Review
Articolo
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)
Articolo
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019)
Articolo
The quality of life of children and adolescents with X-linked agammaglobulinemia.
Articolo
Thymic and bone marrow output in patients with common variable immunodeficiency
Articolo
WASP-WIP DEFICIENCIES: NEW INSIGHTS IN WASP-WIP INTERACTION
Abstract
No Results Found
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