Works matching IS 02719142 AND DT 2015 AND VI 35 AND IP 2
Results: 18
Modulatory Role of Intravenous Gammaglobulin (IgIV) on the in vitro Antibody Response to a Pneumococcal Polysaccharide Antigen.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 206, doi. 10.1007/s10875-014-0120-6
- By:
- Publication type:
- Article
Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 119, doi. 10.1007/s10875-014-0121-5
- By:
- Publication type:
- Article
Fertility, Pregnancies and Outcomes Reported by Females with Common Variable Immune Deficiency and Hypogammaglobulinemia: Results from an Internet-Based Survey.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 125, doi. 10.1007/s10875-014-0123-3
- By:
- Publication type:
- Article
IgA Deficiency and Risk of Cancer: A Population-Based Matched Cohort Study.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 182, doi. 10.1007/s10875-014-0124-2
- By:
- Publication type:
- Article
Combined Immunodeficiency Due to MALT1 Mutations, Treated by Hematopoietic Cell Transplantation.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 135, doi. 10.1007/s10875-014-0125-1
- By:
- Publication type:
- Article
DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 189, doi. 10.1007/s10875-014-0126-0
- By:
- Publication type:
- Article
X-Linked Agammaglobulinemia Associated with B-Precursor Acute Lymphoblastic Leukemia.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 108, doi. 10.1007/s10875-015-0127-7
- By:
- Publication type:
- Article
An Impaired Inflammatory Cytokine Response to Gram-Negative LPS in Human Neonates is Associated with the Defective TLR-Mediated Signaling Pathway.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 218, doi. 10.1007/s10875-015-0128-6
- By:
- Publication type:
- Article
Infectious and Immunologic Phenotype of MECP2 Duplication Syndrome.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 168, doi. 10.1007/s10875-015-0129-5
- By:
- Publication type:
- Article
Coronin-1A: Immune Deficiency in Humans and Mice.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 100, doi. 10.1007/s10875-015-0130-z
- By:
- Publication type:
- Article
Antibody Levels to Bordetella pertussis and Neisseria meningitidis in Immunodeficient Patients Receiving Immunoglobulin Replacement Therapy.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 213, doi. 10.1007/s10875-015-0131-y
- By:
- Publication type:
- Article
Are Patients with X-Linked Agammaglobulinemia at Increased Risk of Developing Acute Lymphoblastic Leukemia?
- Published in:
- 2015
- By:
- Publication type:
- Editorial
Variable Phenotype of Severe Immunodeficiencies Associated with RMRP Gene Mutations.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 147, doi. 10.1007/s10875-015-0135-7
- By:
- Publication type:
- Article
Nijmegen Breakage Syndrome Detected by Newborn Screening for T Cell Receptor Excision Circles (TRECs).
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 227, doi. 10.1007/s10875-015-0136-6
- By:
- Publication type:
- Article
Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 199, doi. 10.1007/s10875-015-0137-5
- By:
- Publication type:
- Article
Monocyte/macrophage-Specific NADPH Oxidase Contributes to Antimicrobial Host Defense in X-CGD.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 2, p. 158, doi. 10.1007/s10875-015-0138-4
- By:
- Publication type:
- Article
A Note from the Editor-in-Chief, Deputy Editor, and Managing Editor.
- Published in:
- 2015
- By:
- Publication type:
- Editorial
Identification of a Novel Mutation in MAGT1 and Progressive Multifocal Leucoencephalopathy in a 58-Year-Old Man with XMEN Disease.
- Published in:
- 2015
- By:
- Publication type:
- Case Study