| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aspergillus fumigatus Skull Bone Osteomyelitis and Native Valve Endocarditis in a Young Boy: an Unusual Presentation of Chronic Granulomatous Disease
|
Anjani, Gummadi
|
|
|
41 |
4 |
p. 814-816
|
artikel
|
| 2 |
C1 Esterase Inhibition: Targeting Multiple Systems in COVID-19
|
Adesanya, T. M. Ayodele
|
|
|
41 |
4 |
p. 729-732
|
artikel
|
| 3 |
Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3
|
Tanita, Kay
|
|
|
41 |
4 |
p. 780-790
|
artikel
|
| 4 |
Complete IFN-γR1 Deficiency in a Boy Due to UPD(6)mat with IFNGR1 Novel Splicing Variant
|
Zhang, Ping
|
|
|
41 |
4 |
p. 834-836
|
artikel
|
| 5 |
Correction to: Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3
|
Tanita, Kay
|
|
|
41 |
4 |
p. 791-794
|
artikel
|
| 6 |
Correction to: Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia
|
Inoue, Kento
|
|
|
41 |
4 |
p. 847
|
artikel
|
| 7 |
Cytokine Profiles Before and After Immune Modulation in Hospitalized Patients with COVID-19
|
Azmy, Veronica
|
|
|
41 |
4 |
p. 738-747
|
artikel
|
| 8 |
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
|
Giardino, Giuliana
|
|
|
41 |
4 |
p. 756-768
|
artikel
|
| 9 |
Failure of Viral-Specific T Cells Administered in Pre-transplant Settings in Children with Inborn Errors of Immunity
|
Alonso, Laura
|
|
|
41 |
4 |
p. 748-755
|
artikel
|
| 10 |
Generalized Pustular Psoriasis in Patients with Interferon Gamma (IFN-γ) Receptor Deficiency and Mycobacterial Infection
|
Xiao, Haijuan
|
|
|
41 |
4 |
p. 829-833
|
artikel
|
| 11 |
Genetic Mosaicism as a Cause of Inborn Errors of Immunity
|
Aluri, Jahnavi
|
|
|
41 |
4 |
p. 718-728
|
artikel
|
| 12 |
Infectious Complications Predict Premature CD8+ T-cell Senescence in CD40 Ligand-Deficient Patients
|
Shin, Junghee J.
|
|
|
41 |
4 |
p. 795-806
|
artikel
|
| 13 |
Inherited TOP2B Mutation: Possible Confirmation of Mutational Hotspots in the TOPRIM Domain
|
Erdős, Melinda
|
|
|
41 |
4 |
p. 817-819
|
artikel
|
| 14 |
Life-Saving, Dose-Adjusted, Targeted Therapy in a Patient with a STAT3 Gain-of-Function Mutation
|
Sarfati, Eytan
|
|
|
41 |
4 |
p. 807-810
|
artikel
|
| 15 |
Novel ADA2 Compound Heterozygous Mutations Resulting in Deficiency of Adenosine Deaminase 2 in a Pair of Siblings
|
Guo, Li
|
|
|
41 |
4 |
p. 837-842
|
artikel
|
| 16 |
Personalized IgG Replacement Therapy for Patients with B cell Inborn Errors of Immunity
|
Bonagura, Vincent R.
|
|
|
41 |
4 |
p. 713-717
|
artikel
|
| 17 |
Stepwise Reversal of Immune Dysregulation Due to STAT1 Gain-of-Function Mutation Following Ruxolitinib Bridge Therapy and Transplantation
|
Kayaoglu, Basak
|
|
|
41 |
4 |
p. 769-779
|
artikel
|
| 18 |
Successful Haploidentical Transplant Using Post-Transplant Cyclophosphamide in a Child with Chronic Granulomatous Disease—First Report from the Indian Subcontinent
|
Bhattad, Sagar
|
|
|
41 |
4 |
p. 820-824
|
artikel
|
| 19 |
The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran
|
Neishabury, Maryam
|
|
|
41 |
4 |
p. 811-813
|
artikel
|
| 20 |
The Impact of the SARS-CoV-2 Pandemic in PID Patients Receiving Ig Replacement Therapy
|
Cekic, Sukru
|
|
|
41 |
4 |
p. 733-737
|
artikel
|
| 21 |
Toxoplasmosis-Associated Hemophagocytic Lymphohistiocytosis in Allogeneic Transplantation
|
Cutini, Ilaria
|
|
|
41 |
4 |
p. 843-846
|
artikel
|
| 22 |
X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase
|
Agrebi, Nourhen
|
|
|
41 |
4 |
p. 825-828
|
artikel
|
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