| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients
|
Hori, Masayuki
|
|
2016
|
37 |
1 |
p. 92-99
|
artikel
|
| 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
|
artikel
|
| 3 |
A 13-Year-Old Child with Lupus-Like Nephritis and 22q11 Microduplication Syndrome
|
Pana, Zoi Dorothea
|
|
2016
|
37 |
1 |
p. 25-26
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
| 7 |
Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan
|
Ono, Shintaro
|
|
2016
|
37 |
1 |
p. 85-91
|
artikel
|
| 8 |
Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan
|
Ono, Shintaro
|
|
|
37 |
1 |
p. 85-91
|
artikel
|
| 9 |
Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing
|
Engelhardt, Karin R.
|
|
2016
|
37 |
1 |
p. 42-50
|
artikel
|
| 10 |
Idiopathic Non-histaminergic Angioedema: Successful Treatment with Omalizumab in Five Patients
|
Faisant, Charles
|
|
2016
|
37 |
1 |
p. 80-84
|
artikel
|
| 11 |
Lack of Clinical Hypersensitivity to Penicillin Antibiotics in Common Variable Immunodeficiency
|
Hartman, Heather
|
|
2016
|
37 |
1 |
p. 22-24
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
| 16 |
Postpartum HLA-Matched Bone Marrow Donation from Mother to Neonate for Reticular Dysgenesis
|
Guilcher, Gregory M. T.
|
|
2016
|
37 |
1 |
p. 29-31
|
artikel
|
| 17 |
Primary Immunodeficiency Classification on Smartphone
|
Jeddane, Leïla
|
|
2016
|
37 |
1 |
p. 1-2
|
artikel
|
| 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
|
artikel
|
| 19 |
Skin Necrosis Following Subcutaneous Immunoglobulin (SCIg)
|
Carne, Emily
|
|
2016
|
37 |
1 |
p. 27-28
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
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