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                             13 gevonden resultaten
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
                             13 gevonden resultaten
 
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