| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 Syndrome
|
Della Mina, Erika
|
|
|
44 |
3 |
|
artikel
|
| 2 |
A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation
|
Erman, Baran
|
|
|
44 |
3 |
|
artikel
|
| 3 |
Clinical Characteristics of Pediatric Patients with LRBA Deficiency in Mexico
|
Liquidano-Perez, Eduardo
|
|
|
44 |
3 |
|
artikel
|
| 4 |
Compound Heterozygosity in Hyper‑IgM Syndrome Type 3: Case Report and Literature Review
|
Majid, Sultan
|
|
|
44 |
3 |
|
artikel
|
| 5 |
Cord Blood Transplantation for Very Early-Onset Inflammatory Bowel Disease Caused by Interleukin-10 Receptor Deficiency
|
Wang, Ping
|
|
|
44 |
3 |
|
artikel
|
| 6 |
Correction to: Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers
|
Patel, Priya K.
|
|
|
44 |
3 |
|
artikel
|
| 7 |
Correction to: Clinical Characteristics of Pediatric Patients with LRBA Deficiency in Mexico
|
Liquidano‑Perez, Eduardo
|
|
|
44 |
3 |
|
artikel
|
| 8 |
Enrichment of Immune Dysregulation Disorders in Adult Patients with Human Inborn Errors of Immunity
|
Segura-Tudela, Alejandro
|
|
|
44 |
3 |
|
artikel
|
| 9 |
Germline HAVCR2/TIM-3 Checkpoint Inhibitor Receptor Deficiency in Recurrent Autoinflammatory Myocarditis
|
Pernaa, Nora
|
|
|
44 |
3 |
|
artikel
|
| 10 |
Inflammatory Proteomic Analysis of 22q11.2 Deletion Syndrome
|
Frusone, Valentina
|
|
|
44 |
3 |
|
artikel
|
| 11 |
Involvement of IL-17 A/IL-17 Receptor A with Neutrophil Recruitment and the Severity of Coronary Arteritis in Kawasaki Disease
|
Lin, I-Chun
|
|
|
44 |
3 |
|
artikel
|
| 12 |
Neuropathologic Impacts of JAK Inhibitor Treatment in Aicardi-Goutières Syndrome
|
Jafarpour, Saba
|
|
|
44 |
3 |
|
artikel
|
| 13 |
Non-Helicobacter pylori Helicobacter Species as a Cause of Refractory Chronic Cellulitis in X-Linked Agammaglobulinemia
|
Zhao, Qianqian
|
|
|
44 |
3 |
|
artikel
|
| 14 |
Novel Presentation of Major Histocompatibility Complex Class II Deficiency with Hemophagocytic Lymphohistiocytosis
|
Alroqi, Fayhan J.
|
|
|
44 |
3 |
|
artikel
|
| 15 |
Parental Engagement in Identifying Information Needs After Newborn Screening for Families of Infants with Suspected Athymia
|
Howley, Evey
|
|
|
44 |
3 |
|
artikel
|
| 16 |
Pharmacokinetics of Baricitinib in Cerebrospinal Fluid and Plasma in a Patient with SPENCD
|
Romano, Micol
|
|
|
44 |
3 |
|
artikel
|
| 17 |
Post-transplant Inflammatory Bowel Disease Associated with Donor-Derived TIM-3 Deficiency
|
Baldrich, Adrian
|
|
|
44 |
3 |
|
artikel
|
| 18 |
Prevalence of Neutralizing Autoantibodies Against Type I Interferon in a Multicenter Cohort of Severe or Critical COVID-19 Cases in Shanghai
|
Shi, Dongling
|
|
|
44 |
3 |
|
artikel
|
| 19 |
Psychosocial Evaluation of Adults with Primary Immunodeficiency
|
Gumusburun, Reyhan
|
|
|
44 |
3 |
|
artikel
|
| 20 |
Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency
|
Rosain, Jérémie
|
|
|
44 |
3 |
|
artikel
|
| 21 |
Successful Treatment of Refractory EBV-Associated Hemophagocytic Lymphohistiocytosis with Combined Emapalumab and PD-1 Blockade
|
Song, Yue
|
|
|
44 |
3 |
|
artikel
|
| 22 |
The Complexity of Being A20: From Biological Functions to Genetic Associations
|
Karri, Urekha
|
|
|
44 |
3 |
|
artikel
|
| 23 |
Thymic Atrophy and Immune Dysregulation in Infants with Complex Congenital Heart Disease
|
Bremer, Sarah-Jolan
|
|
|
44 |
3 |
|
artikel
|
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