Works matching IS 02719142 AND DT 2017 AND VI 37 AND IP 1
Results: 19
Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 67, doi. 10.1007/s10875-016-0339-5
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- Publication type:
- Article
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 36, doi. 10.1007/s10875-016-0342-x
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- Publication type:
- Article
Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 42, doi. 10.1007/s10875-016-0343-9
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- Publication type:
- Article
A 13-Year-Old Child with Lupus-Like Nephritis and 22q11 Microduplication Syndrome.
- Published in:
- 2017
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- Publication type:
- Letter
Idiopathic Non-histaminergic Angioedema: Successful Treatment with Omalizumab in Five Patients.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 80, doi. 10.1007/s10875-016-0345-7
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- Publication type:
- Article
Skin Necrosis Following Subcutaneous Immunoglobulin (SCIg).
- Published in:
- 2017
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- Publication type:
- Letter
Newborn Screening for Severe Primary Immunodeficiency Diseases in Sweden-a 2-Year Pilot TREC and KREC Screening Study.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 51, doi. 10.1007/s10875-016-0347-5
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- Publication type:
- Article
Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 85, doi. 10.1007/s10875-016-0348-4
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- Publication type:
- Article
OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH.
- Published in:
- 2017
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- Publication type:
- Letter
AD Hyper-IgE Syndrome Due to a Novel Loss-of-Function Mutation in STAT3: a Diagnostic Pursuit Won by Clinical Acuity.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Erratum to: Clinical and Molecular Features of 38 Children with Chronic Granulomatous Disease in Mainland China.
- Published in:
- 2017
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- Publication type:
- Erratum
Lack of Clinical Hypersensitivity to Penicillin Antibiotics in Common Variable Immunodeficiency.
- Published in:
- 2017
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- Publication type:
- Letter
Primary Immunodeficiency Classification on Smartphone.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 1, doi. 10.1007/s10875-016-0354-6
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- Publication type:
- Article
Postpartum HLA-Matched Bone Marrow Donation from Mother to Neonate for Reticular Dysgenesis.
- Published in:
- 2017
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- Publication type:
- Letter
Low T Cell Numbers Resembling T−B+ SCID in a Patient with Wiskott-Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations.
- Published in:
- 2017
- By:
- Publication type:
- Letter
A CD57 CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 92, doi. 10.1007/s10875-016-0357-3
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- Publication type:
- Article
Resolution of Multifocal Epstein-Barr Virus-Related Smooth Muscle Tumor in a Patient with GATA2 Deficiency Following Hematopoietic Stem Cell Transplantation.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 61, doi. 10.1007/s10875-016-0360-8
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- Publication type:
- Article
Comments on J Clin Immunol (2014) 34:633-641 DOI 10.1007/s10875-014-0061-0.
- Published in:
- 2017
- By:
- Publication type:
- Letter