| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
ADA2 Deficiency Mimicking Acute Disseminated Encephalomyelitis
|
Ehlers, Lisa
|
|
|
43 |
3 |
p. 536-539
|
artikel
|
| 2 |
Aichivirus: an Emerging Pathogen in Patients with Primary and Secondary B-Cell Deficiency
|
Meyts, Isabelle
|
|
|
43 |
3 |
p. 532-535
|
artikel
|
| 3 |
BT595, a 10% Human Normal Immunoglobulin, for Replacement Therapy of Primary Immunodeficiency Disease: Results of a Subcohort Analysis in Children
|
Kriván, Gergely
|
|
|
43 |
3 |
p. 557-567
|
artikel
|
| 4 |
Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan
|
Inoue, Kento
|
|
|
43 |
3 |
p. 585-594
|
artikel
|
| 5 |
Efficacy and Safety of Interferon-Gamma in Chronic Granulomatous Disease: a Systematic Review and Meta-analysis
|
Lugo Reyes, Saul O.
|
|
|
43 |
3 |
p. 578-584
|
artikel
|
| 6 |
FASCIA Method in the Assessment of Lymphocyte Mitogen Responses in the Laboratory Diagnostics of Primary Immunodeficiencies
|
Lusila, Pauliina
|
|
|
43 |
3 |
p. 653-661
|
artikel
|
| 7 |
Fatal RSV in SCID: the Importance of Infection Prevention Despite Newborn Screening
|
Soomann, Maarja
|
|
|
43 |
3 |
p. 554-556
|
artikel
|
| 8 |
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome
|
Wyatt, Rebecca C.
|
|
|
43 |
3 |
p. 662-669
|
artikel
|
| 9 |
Impact of Genetic Diagnosis on the Outcome of Hematopoietic Stem Cell Transplant in Primary Immunodeficiency Disorders
|
Forlanini, Federica
|
|
|
43 |
3 |
p. 636-646
|
artikel
|
| 10 |
Increased Hazard Risk of First Malignancy in Adults with Undetectable Serum IgE: a Retrospective Cohort Study
|
Weller, Katherine N.
|
|
|
43 |
3 |
p. 568-577
|
artikel
|
| 11 |
Juvenile Neuropsychiatric Systemic Lupus Erythematosus: Identification of Novel Central Neuroinflammation Biomarkers
|
Labouret, Mathilde
|
|
|
43 |
3 |
p. 615-624
|
artikel
|
| 12 |
Knowledge, Attitudes, and Practices of Allergists/Immunologists Regarding Transition of Care for Primary Immunodeficiency Patients
|
Rai, Shipra
|
|
|
43 |
3 |
p. 595-603
|
artikel
|
| 13 |
Lupus Vulgaris Revealing an IκBα Gain of Function Variant
|
Tapiero, Bruce
|
|
|
43 |
3 |
p. 545-547
|
artikel
|
| 14 |
Macrophage Activation Syndrome Complicated by Toxic Epidermal Necrolysis Following SARS-CoV-2 mRNA Vaccination
|
Franzblau, Lauren E.
|
|
|
43 |
3 |
p. 521-524
|
artikel
|
| 15 |
Maternal Gonosomal Mosaicism Causes XIAP Deficiency
|
Tomomasa, Dan
|
|
|
43 |
3 |
p. 525-527
|
artikel
|
| 16 |
Novel Loss of Function (G15D) Mutation on RAC2 in a Family with Combined Immunodeficiency and Increased Levels of Immunoglobulin G, A, and E
|
Duan, Xiaojun
|
|
|
43 |
3 |
p. 604-614
|
artikel
|
| 17 |
Primary Invasive Cutaneous Fusariosis in Patients with STAT3 Hyper-IgE Syndrome
|
Abbara, Salam
|
|
|
43 |
3 |
p. 647-652
|
artikel
|
| 18 |
SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma
|
Lev, Atar
|
|
|
43 |
3 |
p. 625-635
|
artikel
|
| 19 |
Systemic Lupus Erythematosus in Shwachman-Diamond Syndrome: a Novel Phenotype
|
Zhang, Tianyu
|
|
|
43 |
3 |
p. 550-553
|
artikel
|
| 20 |
Through Education and Collaboration to Better Care for Primary Imunodeficiencies in Albania and Kosovo
|
Ismaili-Jaha, Vlora
|
|
|
43 |
3 |
p. 540-544
|
artikel
|
| 21 |
Very Early Onset Inflammatory Bowel Disease Caused by a Novel Dominant Negative Mutation of Caspase Recruitment Domain 11 (CARD11)
|
Hu, Wenhui
|
|
|
43 |
3 |
p. 528-531
|
artikel
|
| 22 |
XLA and Recurrent Conjunctivitis: a Unique Association?
|
Redenbaugh, Vyanka
|
|
|
43 |
3 |
p. 548-549
|
artikel
|
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