| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An infant with ZAP-70 deficiency with disseminated mycobacterial disease
|
Esenboga, Saliha
|
|
2015
|
36 |
2 |
p. 103-106
|
artikel
|
| 2 |
Autosomal Dominant Hyper IgE Syndrome – Treatment Strategies and Clinical Outcomes
|
Flinn, Aisling M.
|
|
2016
|
36 |
2 |
p. 107-109
|
artikel
|
| 3 |
Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency
|
Dang, Tarana Singh
|
|
2016
|
36 |
2 |
p. 117-122
|
artikel
|
| 4 |
Erratum to: Intact IFN-γR1 Expression and Function Distinguishes Langerhans Cell Histiocytosis From Mendelian Susceptibility to Mycobacterial Disease
|
Quispel, Willemijn T.
|
|
2016
|
36 |
2 |
p. 171-172
|
artikel
|
| 5 |
Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey
|
Sterlin, Delphine
|
|
2016
|
36 |
2 |
p. 149-159
|
artikel
|
| 6 |
Is Pulmonary non-Tuberculous Mycobacterial Disease Linked with a High Burden of Latent Cytomegalovirus?
|
Amran, Fathiah S.
|
|
2016
|
36 |
2 |
p. 113-116
|
artikel
|
| 7 |
Life with a Primary Immune Deficiency: a Systematic Synthesis of the Literature and Proposed Research Agenda
|
Similuk, Morgan N.
|
|
2016
|
36 |
2 |
p. 123-133
|
artikel
|
| 8 |
Novel Vasoregulatory Aspects of Hereditary Angioedema: the Role of Arginine Vasopressin, Adrenomedullin and Endothelin-1
|
Kajdácsi, Erika
|
|
2016
|
36 |
2 |
p. 160-170
|
artikel
|
| 9 |
Risk of Infections Among 2100 Individuals with IgA Deficiency: a Nationwide Cohort Study
|
Ludvigsson, Jonas F.
|
|
2016
|
36 |
2 |
p. 134-140
|
artikel
|
| 10 |
The Challenge of Immunoglobulin-G Subclass Deficiency and Specific Polysaccharide Antibody Deficiency – a Dutch Pediatric Cohort Study
|
Schatorjé, Ellen J. H.
|
|
2016
|
36 |
2 |
p. 141-148
|
artikel
|
| 11 |
TNFA, ANXA11 and BTNL2 Polymorphisms in CVID Patients with Granulomatous Disease
|
Boutboul, David
|
|
2016
|
36 |
2 |
p. 110-112
|
artikel
|
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