| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An Unusual Pattern of Premature Cervical Spine Degeneration in STAT3-LOF
|
Mitchell, Amelia L.
|
|
|
41 |
3 |
p. 576-584
|
artikel
|
| 2 |
Benralizumab in Severe and Refractory PDGFRA-Negative Hypereosinophilic Syndrome
|
Alen Coutinho, Iolanda
|
|
|
41 |
3 |
p. 688-690
|
artikel
|
| 3 |
Biomarkers for Early Diagnosis of Hemophagocytic Lymphohistiocytosis in Critically Ill Patients
|
Debaugnies, France
|
|
|
41 |
3 |
p. 658-665
|
artikel
|
| 4 |
Central Nervous System Histoplasma-Associated Post-infectious Inflammatory Response Syndrome (Histo-PIIRS)
|
Dean, Owen
|
|
|
41 |
3 |
p. 545-551
|
artikel
|
| 5 |
Characterization of Infants with Idiopathic Transient and Persistent T Cell Lymphopenia Identified by Newborn Screening—a Single-Center Experience in New York State
|
Jongco, Artemio M.
|
|
|
41 |
3 |
p. 610-620
|
artikel
|
| 6 |
Chronic Disseminated Gonococcal Infection in a Japanese Man with Novel C5 Gene Mutation
|
Ikeuchi, Kazuhiko
|
|
|
41 |
3 |
p. 691-693
|
artikel
|
| 7 |
Clinical and Immunological Analyses of Ten Patients with MIRAGE Syndrome
|
Mitsui-Sekinaka, Kanako
|
|
|
41 |
3 |
p. 709-711
|
artikel
|
| 8 |
Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades’ Experience
|
Benhsaien, Ibtihal
|
|
|
41 |
3 |
p. 631-638
|
artikel
|
| 9 |
Correction to: TREC Screening for WHIM Syndrome
|
Oman Evans, Martin
|
|
|
41 |
3 |
p. 629-630
|
artikel
|
| 10 |
Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies
|
Lodi, Lorenzo
|
|
|
41 |
3 |
p. 603-609
|
artikel
|
| 11 |
Distinctive Features of Kawasaki Disease Following SARS-CoV-2 Infection: a Controlled Study in Paris, France
|
Toubiana, Julie
|
|
|
41 |
3 |
p. 526-535
|
artikel
|
| 12 |
Inflammatory Pseudotumor of Liver and Budd-Chiari Syndrome: a Tale During 10 Years of Follow-up in a Child with Severe Congenital Neutropenia
|
Sugumar, Kiruthiga
|
|
|
41 |
3 |
p. 705-708
|
artikel
|
| 13 |
Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance
|
Oleaga-Quintas, Carmen
|
|
|
41 |
3 |
p. 639-657
|
artikel
|
| 14 |
Liver Abscess in Chronic Granulomatous Disease—Two Decades of Experience from a Tertiary Care Centre in North-West India
|
Pilania, Rakesh Kumar
|
|
|
41 |
3 |
p. 552-564
|
artikel
|
| 15 |
Newborn Screening for Severe Combined Immunodeficiency: 10-Year Experience at a Single Referral Center (2009–2018)
|
Thorsen, Julia
|
|
|
41 |
3 |
p. 595-602
|
artikel
|
| 16 |
Novel IL36RN Mutation Identified in Pediatric-Onset Generalized Pustular Psoriasis Causes IL36 Antagonist Degradation
|
Li, Hongmei
|
|
|
41 |
3 |
p. 701-704
|
artikel
|
| 17 |
Pediatric Demodicosis Associated with Gain-of-Function Variant in STAT1 Presenting as Rosacea-Type Rash
|
Baghad, Bouchra
|
|
|
41 |
3 |
p. 698-700
|
artikel
|
| 18 |
Plasma Exchange to Rescue Patients with Autoantibodies Against Type I Interferons and Life-Threatening COVID-19 Pneumonia
|
de Prost, Nicolas
|
|
|
41 |
3 |
p. 536-544
|
artikel
|
| 19 |
SARS-CoV-2-Induced ARDS Associates with MDSC Expansion, Lymphocyte Dysfunction, and Arginine Shortage
|
Reizine, Florian
|
|
|
41 |
3 |
p. 515-525
|
artikel
|
| 20 |
Serum Sp17 Autoantibody Serves as a Potential Specific Biomarker in Patients with SAPHO Syndrome
|
You, Hongqin
|
|
|
41 |
3 |
p. 565-575
|
artikel
|
| 21 |
Soluble Interleukin-2 Receptor Is a Promising Serum Biomarker for Granulomatous Disease in Common Variable Immune Deficiency
|
van Stigt, Astrid C.
|
|
|
41 |
3 |
p. 694-697
|
artikel
|
| 22 |
STING-Mediated Lung Inflammation and Beyond
|
Frémond, Marie-Louise
|
|
|
41 |
3 |
p. 501-514
|
artikel
|
| 23 |
Successful Hematopoietic Stem Cell Transplantation for Autosomal Recessive STAT1 Complete Deficiency
|
Karakawa, Shuhei
|
|
|
41 |
3 |
p. 684-687
|
artikel
|
| 24 |
The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee
|
Tangye, Stuart G.
|
|
|
41 |
3 |
p. 666-679
|
artikel
|
| 25 |
TREC Screening for WHIM Syndrome
|
Evans, Martin Oman
|
|
|
41 |
3 |
p. 621-628
|
artikel
|
| 26 |
Uncontrolled Epstein-Barr Virus as an Atypical Presentation of Deficiency in ADA2 (DADA2)
|
Brooks, Joel P.
|
|
|
41 |
3 |
p. 680-683
|
artikel
|
| 27 |
Use of Complementary and Alternative Medicine in Patients with Primary Immunodeficiency: a Multicentric Analysis of 101 Patients
|
Harasim, Anna S.
|
|
|
41 |
3 |
p. 585-594
|
artikel
|
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