nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency
|
Rosain, Jérémie |
|
2018 |
38 |
5 |
p. 617-627 |
artikel |
2 |
Biweekly Hizentra® in Primary Immunodeficiency: a Multicenter, Observational Cohort Study (IBIS)
|
Vultaggio, Alessandra |
|
2018 |
38 |
5 |
p. 602-609 |
artikel |
3 |
Clearing Vaccine-Derived Poliovirus Infection Following Hematopoietic Stem Cell Transplantation: a Case Report and Review of Literature
|
Shaghaghi, Mohammadreza |
|
2018 |
38 |
5 |
p. 610-616 |
artikel |
4 |
Deficiency of Adenosine Deaminase 2 (DADA2): Updates on the Phenotype, Genetics, Pathogenesis, and Treatment
|
Meyts, Isabelle |
|
2018 |
38 |
5 |
p. 569-578 |
artikel |
5 |
IKBA S32 Mutations Underlie Ectodermal Dysplasia with Immunodeficiency and Severe Noninfectious Systemic Inflammation
|
Moriya, Kunihiko |
|
2018 |
38 |
5 |
p. 543-545 |
artikel |
6 |
Low Rates of Poliovirus Antibodies in Primary Immunodeficiency Patients on Regular Intravenous Immunoglobulin Treatment
|
Costa-Carvalho, Beatriz T. |
|
2018 |
38 |
5 |
p. 628-634 |
artikel |
7 |
Reflex Testing of Immunoglobulins in Patients with Total Serum IgE < 2 kU/L
|
Campisi, Lisa |
|
2018 |
38 |
5 |
p. 550-552 |
artikel |
8 |
Renal Disease in Chronic Granulomatous Disease: Data from the USIDNET Registry
|
Sacco, Keith A. |
|
2018 |
38 |
5 |
p. 556-557 |
artikel |
9 |
Severe Congenital Neutropenia associated with SRP54 mutation in 22q11.2 Deletion Syndrome: Hematopoietic Stem Cell Transplantation Results in Correction of Neutropenia with Adequate Immune Reconstitution
|
Carden, Marcus A. |
|
2018 |
38 |
5 |
p. 546-549 |
artikel |
10 |
The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions
|
Rieux-Laucat, Frédéric |
|
2018 |
38 |
5 |
p. 558-568 |
artikel |
11 |
The Treatment of Inflammatory Bowel Disease in Patients with Selected Primary Immunodeficiencies
|
Shouval, Dror S. |
|
2018 |
38 |
5 |
p. 579-588 |
artikel |
12 |
Transient Marked Increase of γδ T Cells in WHIM Syndrome After Successful HSCT
|
Kawahara, Yuta |
|
2018 |
38 |
5 |
p. 553-555 |
artikel |
13 |
Utility of Ruxolitinib in a Child with Chronic Mucocutaneous Candidiasis Caused by a Novel STAT1 Gain-of-Function Mutation
|
Bloomfield, Markéta |
|
2018 |
38 |
5 |
p. 589-601 |
artikel |