Digital Library
Close Browse articles from a journal
     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
                                       All articles of the corresponding issues
 
                             21 results found
no title author magazine year volume issue page(s) type
1 A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients Hori, Masayuki
2016
37 1 p. 92-99
article
2 AD Hyper-IgE Syndrome Due to a Novel Loss-of-Function Mutation in STAT3: a Diagnostic Pursuit Won by Clinical Acuity Moens, Leen
2016
37 1 p. 12-17
article
3 A 13-Year-Old Child with Lupus-Like Nephritis and 22q11 Microduplication Syndrome Pana, Zoi Dorothea
2016
37 1 p. 25-26
article
4 Comments on J Clin Immunol (2014) 34:633–641 DOI 10.1007/s10875-014-0061-0 Roos, Dirk
2016
37 1 p. 3-4
article
5 Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography Bondioni, Maria Pia
2016
37 1 p. 36-41
article
6 Erratum to: Clinical and Molecular Features of 38 Children with Chronic Granulomatous Disease in Mainland China Xu, Huan
2016
37 1 p. 5-6
article
7 Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan Ono, Shintaro
2016
37 1 p. 85-91
article
8 Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan Ono, Shintaro

37 1 p. 85-91
article
9 Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing Engelhardt, Karin R.
2016
37 1 p. 42-50
article
10 Idiopathic Non-histaminergic Angioedema: Successful Treatment with Omalizumab in Five Patients Faisant, Charles
2016
37 1 p. 80-84
article
11 Lack of Clinical Hypersensitivity to Penicillin Antibiotics in Common Variable Immunodeficiency Hartman, Heather
2016
37 1 p. 22-24
article
12 Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection Brigida, Immacolata
2016
37 1 p. 32-35
article
13 Low T Cell Numbers Resembling T−B+ SCID in a Patient with Wiskott–Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations Cagdas, Deniz
2016
37 1 p. 18-21
article
14 Newborn Screening for Severe Primary Immunodeficiency Diseases in Sweden—a 2-Year Pilot TREC and KREC Screening Study Barbaro, Michela
2016
37 1 p. 51-60
article
15 OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH Ricci, Silvia
2016
37 1 p. 7-11
article
16 Postpartum HLA-Matched Bone Marrow Donation from Mother to Neonate for Reticular Dysgenesis Guilcher, Gregory M. T.
2016
37 1 p. 29-31
article
17 Primary Immunodeficiency Classification on Smartphone Jeddane, Leïla
2016
37 1 p. 1-2
article
18 Resolution of Multifocal Epstein-Barr Virus-Related Smooth Muscle Tumor in a Patient with GATA2 Deficiency Following Hematopoietic Stem Cell Transplantation Parta, Mark
2016
37 1 p. 61-66
article
19 Skin Necrosis Following Subcutaneous Immunoglobulin (SCIg) Carne, Emily
2016
37 1 p. 27-28
article
20 Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study Suzuki, Tasuku
2016
37 1 p. 67-79
article
21 Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study Suzuki, Tasuku

37 1 p. 67-79
article
                             21 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands