| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome
|
Cagdas, Deniz
|
|
2018
|
38 |
4 |
p. 484-493
|
artikel
|
| 2 |
Antinuclear Antibody-Positive Juvenile Idiopathic Arthritis Despite IRAK-4 Deficiency
|
Hügle, Boris
|
|
2018
|
38 |
4 |
p. 450-453
|
artikel
|
| 3 |
Aortic Calcification in a Patient with a Gain-of-Function STAT1 Mutation
|
Smyth, Anna E.
|
|
2018
|
38 |
4 |
p. 468-470
|
artikel
|
| 4 |
Autosomal Dominant IFN-γR1 Deficiency Presenting with both Atypical Mycobacteriosis and Tuberculosis in a BCG-Vaccinated South African Patient
|
Glanzmann, Brigitte
|
|
2018
|
38 |
4 |
p. 460-463
|
artikel
|
| 5 |
Cerebral Lymphoproliferation in a Patient with Kabuki Syndrome
|
Marzollo, Antonio
|
|
2018
|
38 |
4 |
p. 475-477
|
artikel
|
| 6 |
Correction to: Assessment of Local Adverse Reactions to Subcutaneous Immunoglobulin (SCIG) in Clinical Trials
|
Ballow, Mark
|
|
2018
|
38 |
4 |
p. 539
|
artikel
|
| 7 |
Correction to: Circulating T Cells of Patients with Nijmegen Breakage Syndrome Show Signs of Senescence
|
Meijers, Ruud W. J.
|
|
2018
|
38 |
4 |
p. 538
|
artikel
|
| 8 |
Correction to: Raised Serum IL-8 Levels Are Associated with Excessive Fatigue in Female Carriers of X-Linked Chronic Granulomatous Disease in the UK
|
Battersby, Alexandra C.
|
|
2018
|
38 |
4 |
p. 537
|
artikel
|
| 9 |
Correction to: Use of Genetic Testing for Primary Immunodeficiency Patients
|
Heimall, Jennifer R.
|
|
2018
|
38 |
4 |
p. 540-541
|
artikel
|
| 10 |
Disseminated Cutaneous Warts in X-Linked Hyper IgM Syndrome
|
Ho, Hsi-en
|
|
2018
|
38 |
4 |
p. 454-456
|
artikel
|
| 11 |
Dual Threat of Epstein-Barr Virus: an Autopsy Case Report of HIV-Positive Plasmablastic Lymphoma Complicating EBV-Associated Hemophagocytic Lymphohistiocytosis
|
Koizumi, Yusuke
|
|
2018
|
38 |
4 |
p. 478-483
|
artikel
|
| 12 |
Editorial
|
Casanova, Jean-Laurent
|
|
2018
|
38 |
4 |
p. 445-446
|
artikel
|
| 13 |
First Identification of an Inherited TPSAB1 Quintuplication in a Patient with Clonal Mast Cell Disease
|
Sabato, Vito
|
|
2018
|
38 |
4 |
p. 457-459
|
artikel
|
| 14 |
Insights into Mutation Effect in Three Poikiloderma with Neutropenia Patients by Transcript Analysis and Disease Evolution of Reported Patients with the Same Pathogenic Variants
|
Colombo, Elisa A.
|
|
2018
|
38 |
4 |
p. 494-502
|
artikel
|
| 15 |
Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency
|
Sologuren, Ithaisa
|
|
2018
|
38 |
4 |
p. 513-526
|
artikel
|
| 16 |
Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency
|
Sologuren, Ithaisa
|
|
|
38 |
4 |
p. 513-526
|
artikel
|
| 17 |
Novel LRBA Mutation and Possible Germinal Mosaicism in a Slavic Family
|
Sharapova, Svetlana O.
|
|
2018
|
38 |
4 |
p. 471-474
|
artikel
|
| 18 |
Rapid Push vs Pump-Infused Subcutaneous Immunoglobulin Treatment: a Randomized Crossover Study of Quality of Life in Primary Immunodeficiency Patients
|
Bienvenu, Boris
|
|
2018
|
38 |
4 |
p. 503-512
|
artikel
|
| 19 |
The International Alliance of Primary Immune Deficiency Societies
|
Gennery, Andrew R.
|
|
2018
|
38 |
4 |
p. 447-449
|
artikel
|
| 20 |
T+ NK+ IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency
|
Stepensky, Polina
|
|
|
38 |
4 |
p. 527-536
|
artikel
|
| 21 |
T+ NK+ IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency
|
Stepensky, Polina
|
|
2018
|
38 |
4 |
p. 527-536
|
artikel
|
| 22 |
Treatment of Intracerebral Lesions with Abatacept in a CTLA4-Haploinsufficient Patient
|
Leeuwen, Ester M. van
|
|
2018
|
38 |
4 |
p. 464-467
|
artikel
|
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