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2. The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1
3. Adequate Patient’s Outcome Achieved with Short Immunoglobulin Replacement Intervals in Severe Antibody Deficiencies
4. The Case for Mandatory Newborn Screening for Severe Combined Immunodeficiency (SCID)
5. Complete Factor I Deficiency Due to Dysfunctional Factor I with Recurrent Aseptic Meningo-Encephalitis
6. The Natural History of Children with Severe Combined Immunodeficiency: Baseline Features of the First Fifty Patients of the Primary Immune Deficiency Treatment Consortium Prospective Study 6901
7. MicroRNA-21 in Scleroderma Fibrosis and its Function in TGF-β- Regulated Fibrosis-Related Genes Expression
8. The Spread of the J Project
9. Biology of Human Pentraxin 3 (PTX3) in Acute and Chronic Kidney Disease
10. A Non-invasive Diagnosis of Histiocytic Necrotizing Lymphadenitis by Means of Gene Expression Profile Analysis of Peripheral Blood Mononuclear Cells
11. Characterization of Th1- and Th2-associated Chemokine Receptor Expression in Spleens of Patients with Immune Thrombocytopenia
12. The Possible Roles of OPN-Regulated CEACAM1 Expression in Promoting the Survival of Activated T Cells and the Apoptosis of Oral Keratinocytes in Oral Lichen Planus Patients
13. Active Immunological Profile Is Associated with Systemic Sjögren’s Syndrome
14. Allogeneic Haematopoietic Stem Cell Transplantation as Therapy for Chronic Granulomatous Disease—Single Centre Experience
15. TGF-β and Regulatory T Cell in Immunity and Autoimmunity
16. Association of Graves’ Disease and Prevalence of Circulating IFN-γ-producing CD28− T Cells
17. Phenotype–Genotype Analysis of Cryopyrin-Associated Periodic Syndromes (CAPS): Description of a Rare Non-Exon 3 and a Novel CIAS1 Missense Mutation
18. Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
19. Autosomal Recessive Agammaglobulinemia Due to a Homozygous Mutation in PIK3R1
20. Mechanisms of Sustained Neutrophilia in Patient WHIM-09, Cured of WHIM Syndrome by Chromothripsis
21. Chronic Diarrhea in Common Variable Immunodeficiency: a Case Series and Review of the Literature
22. Newborn Screening for Primary Immunodeficiency Diseases: History, Current and Future Practice
23. Modulation of the Interleukin-21 Pathway with Interleukin-4 Distinguishes Common Variable Immunodeficiency Patients with More Non-infectious Clinical Complications
24. Immunodeficiency in Bloom’s Syndrome
25. Multiple Presentations of LRBA Deficiency: a Single-Center Experience
26. Autoimmune Cytopenias and Associated Conditions in CVID: a Report From the USIDNET Registry
27. DOCK8 Deficiency Presenting as an IPEX-Like Disorder
28. Functional Evaluation of an IKBKG Variant Suspected to Cause Immunodeficiency Without Ectodermal Dysplasia
29. Emerging Infections and Pertinent Infections Related to Travel for Patients with Primary Immunodeficiencies
30. Neutropenia in Patients with Common Variable Immunodeficiency: a Rare Event Associated with Severe Outcome
31. Adenosine Deaminase (ADA)-Deficient Severe Combined Immune Deficiency (SCID): Molecular Pathogenesis and Clinical Manifestations
32. Rituximab Restores IFN-γ-STAT1 Function and Ameliorates Disseminated Mycobacterium avium Infection in a Patient with Anti-Interferon-γ Autoantibody
33. Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency
34. Detection of Sp110 by Flow Cytometry and Application to Screening Patients for Veno-occlusive Disease with Immunodeficiency
35. Severe Enteropathy and Hypogammaglobulinemia Complicating Refractory Mycobacterium tuberculosis Complex Disseminated Disease in a Child with IL-12Rβ1 Deficiency
36. A Personalized Diagnostic and Treatment Approach for Macrophage Activation Syndrome and Secondary Hemophagocytic Lymphohistiocytosis in Adults
37. Helicobacter bilis-Associated Suppurative Cholangitis in a Patient with X-Linked Agammaglobulinemia
38. Gastrointestinal Manifestations of STAT3-Deficient Hyper-IgE Syndrome
39. Early Versus Late Diagnosis of Complement Factor I Deficiency: Clinical Consequences Illustrated in Two Families with Novel Homozygous CFI Mutations
40. Preferential Reduction of Circulating Innate Lymphoid Cells Type 2 in Patients with Common Variable Immunodeficiency with Secondary Complications Is Part of a Broader Immune Dysregulation
41. Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis
42. FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
43. Long-Term Outcome of Adenosine Deaminase-Deficient Patients—a Single-Center Experience
44. Immunodeficiency in Two Female Patients with Incontinentia Pigmenti with Heterozygous NEMO Mutation Diagnosed by LPS Unresponsiveness
45. Delayed Puberty and Gonadal Failure in Patients with HAX1 Mutation
46. Loss of NHEJ1 Protein Due to a Novel Splice Site Mutation in a Family Presenting with Combined Immunodeficiency, Microcephaly, and Growth Retardation and Literature Review
47. A Multicentre Study on the Efficacy, Safety and Pharmacokinetics of IqYmune®, a Highly Purified 10% Liquid Intravenous Immunoglobulin, in Patients with Primary Immune Deficiency
48. Two Sides of the Same Coin: Pediatric-Onset and Adult-Onset Common Variable Immune Deficiency
49. Allogeneic Reduced-Intensity Hematopoietic Stem Cell Transplantation for Chronic Granulomatous Disease: a Single-Center Prospective Trial
50. Efficacy and Safety of Human Intravenous Immunoglobulin 10% (Panzyga®) in Patients with Primary Immunodeficiency Diseases: a Two-Stage, Multicenter, Prospective, Open-Label Study
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