nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Anti-GM-CSF Autoantibodies and Cryptococcus neoformans var. grubii CNS Vasculitis
|
Perrineau, Segolene |
|
|
40 |
5 |
p. 767-769 |
artikel |
2 |
An Update on XMEN Disease
|
Ravell, Juan C. |
|
|
40 |
5 |
p. 671-681 |
artikel |
3 |
A Systematic Review and Meta-regression Analysis on the Impact of Increasing IgG Trough Level on Infection Rates in Primary Immunodeficiency Patients on Intravenous IgG Therapy
|
Lee, Jian Lynn |
|
|
40 |
5 |
p. 682-698 |
artikel |
4 |
Chronic Granulomatous Disease with the McLeod Phenotype: a French National Retrospective Case Series
|
Lhomme, Faustine |
|
|
40 |
5 |
p. 752-762 |
artikel |
5 |
Correction to: A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency
|
Coignard-Biehler, Hélène |
|
|
40 |
5 |
p. 786-787 |
artikel |
6 |
Correction to: 2020 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference
|
Kalashnikova, Tatiana |
|
|
40 |
5 |
p. 788 |
artikel |
7 |
Everolimus-Induced Remission of Classic Kaposi’s Sarcoma Secondary to Cryptic Splicing Mediated CTLA4 Haploinsufficiency
|
Yap, Jin Yan |
|
|
40 |
5 |
p. 774-779 |
artikel |
8 |
Haploinsufficiency of A20 Due to Novel Mutations in TNFAIP3
|
He, Tingyan |
|
|
40 |
5 |
p. 741-751 |
artikel |
9 |
Incidence of SCID in Germany from 2014 to 2015 an ESPED* Survey on Behalf of the API*** Erhebungseinheit für Seltene Pädiatrische Erkrankungen in Deutschland (German Paediatric Surveillance Unit) ** Arbeitsgemeinschaft Pädiatrische Immunologie
|
Shai, Sonu |
|
|
40 |
5 |
p. 708-717 |
artikel |
10 |
Prognostic Value of Blood-Based Inflammatory Biomarkers in Secondary Hemophagocytic Lymphohistiocytosis
|
Huang, Jiayu |
|
|
40 |
5 |
p. 718-728 |
artikel |
11 |
Successful Artery Embolization in a Patient with Autoimmune Lymphoproliferative Syndrome Associated with Splenic Rupture
|
Kohrogi, Kensaku |
|
|
40 |
5 |
p. 780-782 |
artikel |
12 |
The Association of Fetal Thymus Size with Subsequent T Cell Counts in 22q11.2 Deletion Syndrome
|
Dou, Ying |
|
|
40 |
5 |
p. 783-785 |
artikel |
13 |
The Clinical Immunogenomics Research Consortium Australasia (CIRCA): a Distributed Network Model for Genomic Healthcare Delivery
|
Phan, Tri Giang |
|
|
40 |
5 |
p. 763-766 |
artikel |
14 |
The Konya Declaration for Patients with Primary Immunodeficiencies
|
Maródi, László |
|
|
40 |
5 |
p. 770-773 |
artikel |
15 |
Thinking Beyond HLH: Clinical Features of Patients with Concurrent Presentation of Hemophagocytic Lymphohistiocytosis and Thrombotic Microangiopathy
|
Gloude, Nicholas J. |
|
|
40 |
5 |
p. 699-707 |
artikel |
16 |
Whole-Exome Sequencing-Based Approach for Germline Mutations in Patients with Inborn Errors of Immunity
|
Okano, Tsubasa |
|
|
40 |
5 |
p. 729-740 |
artikel |