| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Clinical Approach to a Child with Hypoalbuminemia and Lymphopenia
|
Köstel-Bal, Ayse Sevgi
|
|
2016
|
36 |
4 |
p. 370-373
|
artikel
|
| 2 |
A ‘Too Negative’ ANA Test Predicts Antibody Deficiency
|
Recher, Mike
|
|
2016
|
36 |
4 |
p. 374-376
|
artikel
|
| 3 |
Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease
|
Vece, Timothy J.
|
|
2016
|
36 |
4 |
p. 377-387
|
artikel
|
| 4 |
Erratum to: Adenosine Deaminase Deficient Severe Combined Immunodeficiency Presenting as Atypical Haemolytic Uraemic Syndrome
|
Nikolajeva, Olga
|
|
2016
|
36 |
4 |
p. 413
|
artikel
|
| 5 |
Immune Complex-Mediated Glomerulonephritis in a Patient with Wiskott–Aldrich Syndrome
|
Shigemura, Tomonari
|
|
2016
|
36 |
4 |
p. 357-359
|
artikel
|
| 6 |
Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals
|
Felgentreff, Kerstin
|
|
2016
|
36 |
4 |
p. 341-353
|
artikel
|
| 7 |
Myelodysplastic Syndrome and Acute Lymphocytic Leukemia in Common Variable Immunodeficiency (CVID)
|
Toh, Jennifer
|
|
2016
|
36 |
4 |
p. 366-369
|
artikel
|
| 8 |
Novel Mutations Causing C5 Deficiency in Three North-African Families
|
Colobran, Roger
|
|
2016
|
36 |
4 |
p. 388-396
|
artikel
|
| 9 |
Presenting features and platelet anomalies in WAS: one centre’s experience
|
Tsilifis, Christo
|
|
2016
|
36 |
4 |
p. 354-356
|
artikel
|
| 10 |
Secondary Antibody Deficiency in Glucocorticoid Therapy Clearly Differs from Primary Antibody Deficiency
|
Wirsum, Clemens
|
|
2016
|
36 |
4 |
p. 406-412
|
artikel
|
| 11 |
Spondylodiscitis in a Boy with X-linked Agammaglobulinemia: an Unusual Occurrence
|
Bhattad, Sagar
|
|
2016
|
36 |
4 |
p. 360-362
|
artikel
|
| 12 |
The Evolving Landscape of Primary Immunodeficiencies
|
Gennery, Andrew R.
|
|
2016
|
36 |
4 |
p. 339-340
|
artikel
|
| 13 |
Visceral Leishmaniasis May Unmask X-linked Hyper-IgM Syndrome
|
Gonzalez-Granado, Luis Ignacio
|
|
2016
|
36 |
4 |
p. 363-365
|
artikel
|
| 14 |
WHIM Syndrome Caused by Waldenström’s Macroglobulinemia-Associated Mutation CXCR4L329fs
|
Liu, Qian
|
|
2016
|
36 |
4 |
p. 397-405
|
artikel
|
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