Found: 20
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Novel LRBA Mutation and Possible Germinal Mosaicism in a Slavic Family.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Aortic Calcification in a Patient with a Gain-of-Function STAT1 Mutation.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Cerebral Lymphoproliferation in a Patient with Kabuki Syndrome.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Editorial.
- Published in:
- 2018
- By:
- Publication type:
- Editorial
The International Alliance of Primary Immune Deficiency Societies.
- Published in:
- 2018
- By:
- Publication type:
- Editorial
Treatment of Intracerebral Lesions with Abatacept in a CTLA4-Haploinsufficient Patient.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
T<sup>+</sup> NK<sup>+</sup> IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 527, doi. 10.1007/s10875-018-0514-y
- By:
- Publication type:
- Article
Correction to: Use of Genetic Testing for Primary Immunodeficiency Patients.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 513, doi. 10.1007/s10875-018-0512-0
- By:
- Publication type:
- Article
Autosomal Dominant IFN-γR1 Deficiency Presenting with both Atypical Mycobacteriosis and Tuberculosis in a BCG-Vaccinated South African Patient.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Insights into Mutation Effect in Three Poikiloderma with Neutropenia Patients by Transcript Analysis and Disease Evolution of Reported Patients with the Same Pathogenic Variants.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 494, doi. 10.1007/s10875-018-0508-9
- By:
- Publication type:
- Article
Rapid Push vs Pump-Infused Subcutaneous Immunoglobulin Treatment: a Randomized Crossover Study of Quality of Life in Primary Immunodeficiency Patients.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 503, doi. 10.1007/s10875-018-0507-x
- By:
- Publication type:
- Article
First Identification of an Inherited TPSAB1 Quintuplication in a Patient with Clonal Mast Cell Disease.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Disseminated Cutaneous Warts in X-Linked Hyper IgM Syndrome.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Correction to: Assessment of Local Adverse Reactions to Subcutaneous Immunoglobulin (SCIG) in Clinical Trials.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Correction to: Circulating T Cells of Patients with Nijmegen Breakage Syndrome Show Signs of Senescence.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Correction to: Raised Serum IL-8 Levels Are Associated with Excessive Fatigue in Female Carriers of X-Linked Chronic Granulomatous Disease in the UK.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Antinuclear Antibody-Positive Juvenile Idiopathic Arthritis Despite IRAK-4 Deficiency.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Dual Threat of Epstein-Barr Virus: an Autopsy Case Report of HIV-Positive Plasmablastic Lymphoma Complicating EBV-Associated Hemophagocytic Lymphohistiocytosis.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 484, doi. 10.1007/s10875-018-0496-9
- By:
- Publication type:
- Article