nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Novel Missense LIG4 Mutation in a Patient With a Phenotype Mimicking Behçet’s Disease
|
Taskiran, Ekim Z. |
|
2019 |
39 |
1 |
p. 99-105 |
artikel |
2 |
A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis
|
Sharafian, Samin |
|
|
39 |
1 |
p. 11-14 |
artikel |
3 |
A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis
|
Sharafian, Samin |
|
2019 |
39 |
1 |
p. 11-14 |
artikel |
4 |
Autoimmunity and Inflammation in CVID: a Possible Crosstalk between Immune Activation, Gut Microbiota, and Epigenetic Modifications
|
Jørgensen, Silje F. |
|
2018 |
39 |
1 |
p. 30-36 |
artikel |
5 |
Childhood Hodgkin Lymphoma: Think DADA2
|
Alabbas, Fahad |
|
2019 |
39 |
1 |
p. 26-29 |
artikel |
6 |
Damaging BTK Variant Demonstrated by Carrier, Allele-Specific BTK Expression in B Cells and Monocytes
|
Bausch-Jurken, Mary T. |
|
2019 |
39 |
1 |
p. 23-25 |
artikel |
7 |
DDX58 and Classic Singleton-Merten Syndrome
|
Ferreira, Carlos R. |
|
2018 |
39 |
1 |
p. 75-80 |
artikel |
8 |
Differing Performance of the Warning Signs for Immunodeficiency in the Diagnosis of Pediatric Versus Adult Patients in a Two-Center Tertiary Referral Population
|
Bjelac, Jaclyn A. |
|
2019 |
39 |
1 |
p. 90-98 |
artikel |
9 |
Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation
|
Kiykim, Ayca |
|
2018 |
39 |
1 |
p. 37-44 |
artikel |
10 |
Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation
|
Kiykim, Ayca |
|
|
39 |
1 |
p. 37-44 |
artikel |
11 |
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group
|
Schütz, Katharina |
|
2018 |
39 |
1 |
p. 45-54 |
artikel |
12 |
Lymphocyte Apoptosis and FAS Expression in Patients with 22q11.2 Deletion Syndrome
|
Aresvik, Dina M. |
|
2018 |
39 |
1 |
p. 65-74 |
artikel |
13 |
Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occurrence
|
Rikhi, Rashmi |
|
2019 |
39 |
1 |
p. 7-10 |
artikel |
14 |
MonoMAC Syndrome Caused by a Novel GATA2 Mutation Successfully Treated by Allogeneic Hematopoietic Stem Cell Transplantation
|
Moraes-Fontes, Maria Francisca |
|
2018 |
39 |
1 |
p. 4-6 |
artikel |
15 |
Mosaicism of an ELANE Mutation in an Asymptomatic Mother
|
Shigemura, Tomonari |
|
2019 |
39 |
1 |
p. 106-111 |
artikel |
16 |
Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus-Associated Granuloma
|
Perelygina, Ludmila |
|
2019 |
39 |
1 |
p. 112-117 |
artikel |
17 |
Progressive Multifocal Leukoencephalopathy in Primary Immunodeficiencies
|
Hadjadj, Jérôme |
|
2018 |
39 |
1 |
p. 55-64 |
artikel |
18 |
Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders
|
Buchbinder, David |
|
2019 |
39 |
1 |
p. 81-89 |
artikel |
19 |
Successful Bone Marrow Transplantation for XMEN: Hemorrhagic Risk Uncovered
|
Dimitrova, Dimana |
|
2018 |
39 |
1 |
p. 1-3 |
artikel |
20 |
Successful Treatment with SCIG of a Child with Refractory Chronic ITP
|
Karastaneva, Anna |
|
2019 |
39 |
1 |
p. 19-22 |
artikel |
21 |
TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia
|
Paradis, C. |
|
2019 |
39 |
1 |
p. 118-125 |
artikel |
22 |
Two Prenatal Cases of Hyper-IgE Syndrome
|
Egawa, Makiko |
|
2019 |
39 |
1 |
p. 15-18 |
artikel |