| no |
title |
author |
magazine |
year |
volume |
issue |
page(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
|
article
|
| 2 |
A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis
|
Sharafian, Samin
|
|
|
39 |
1 |
p. 11-14
|
article
|
| 3 |
A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis
|
Sharafian, Samin
|
|
2019
|
39 |
1 |
p. 11-14
|
article
|
| 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
|
article
|
| 5 |
Childhood Hodgkin Lymphoma: Think DADA2
|
Alabbas, Fahad
|
|
2019
|
39 |
1 |
p. 26-29
|
article
|
| 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
|
article
|
| 7 |
DDX58 and Classic Singleton-Merten Syndrome
|
Ferreira, Carlos R.
|
|
2018
|
39 |
1 |
p. 75-80
|
article
|
| 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
|
article
|
| 9 |
Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation
|
Kiykim, Ayca
|
|
2018
|
39 |
1 |
p. 37-44
|
article
|
| 10 |
Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation
|
Kiykim, Ayca
|
|
|
39 |
1 |
p. 37-44
|
article
|
| 11 |
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group
|
Schütz, Katharina
|
|
2018
|
39 |
1 |
p. 45-54
|
article
|
| 12 |
Lymphocyte Apoptosis and FAS Expression in Patients with 22q11.2 Deletion Syndrome
|
Aresvik, Dina M.
|
|
2018
|
39 |
1 |
p. 65-74
|
article
|
| 13 |
Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occurrence
|
Rikhi, Rashmi
|
|
2019
|
39 |
1 |
p. 7-10
|
article
|
| 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
|
article
|
| 15 |
Mosaicism of an ELANE Mutation in an Asymptomatic Mother
|
Shigemura, Tomonari
|
|
2019
|
39 |
1 |
p. 106-111
|
article
|
| 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
|
article
|
| 17 |
Progressive Multifocal Leukoencephalopathy in Primary Immunodeficiencies
|
Hadjadj, Jérôme
|
|
2018
|
39 |
1 |
p. 55-64
|
article
|
| 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
|
article
|
| 19 |
Successful Bone Marrow Transplantation for XMEN: Hemorrhagic Risk Uncovered
|
Dimitrova, Dimana
|
|
2018
|
39 |
1 |
p. 1-3
|
article
|
| 20 |
Successful Treatment with SCIG of a Child with Refractory Chronic ITP
|
Karastaneva, Anna
|
|
2019
|
39 |
1 |
p. 19-22
|
article
|
| 21 |
TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia
|
Paradis, C.
|
|
2019
|
39 |
1 |
p. 118-125
|
article
|
| 22 |
Two Prenatal Cases of Hyper-IgE Syndrome
|
Egawa, Makiko
|
|
2019
|
39 |
1 |
p. 15-18
|
article
|
Journal description