| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Female Patient with Incomplete Hemophagocytic Lymphohistiocytosis Caused by a Heterozygous XIAP Mutation Associated with Non-Random X-Chromosome Inactivation Skewed Towards the Wild-Type XIAP Allele
|
Yang, Xi
|
|
2015
|
35 |
3 |
p. 244-248
|
artikel
|
| 2 |
A mutation in the human tetraspanin CD81 gene is expressed as a truncated protein but does not enable CD19 maturation and cell surface expression
|
Vences-Catalán, Felipe
|
|
2015
|
35 |
3 |
p. 254-263
|
artikel
|
| 3 |
2015 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference
|
|
|
2015
|
35 |
3 |
p. 305-328
|
artikel
|
| 4 |
2015 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference
|
|
|
|
35 |
3 |
p. 305-328
|
artikel
|
| 5 |
Familial Hepatopulmonary Syndrome in Common Variable Immunodeficiency
|
Holmes, S. N.
|
|
2015
|
35 |
3 |
p. 302-304
|
artikel
|
| 6 |
Human Disease Phenotypes Associated With Mutations in TREX1
|
Rice, Gillian I.
|
|
2015
|
35 |
3 |
p. 235-243
|
artikel
|
| 7 |
Long-Term Follow-up of STAT5B Deficiency in Three Argentinian Patients: Clinical and Immunological Features
|
Bezrodnik, Liliana
|
|
2015
|
35 |
3 |
p. 264-272
|
artikel
|
| 8 |
Overlap of Familial Mediterranean Fever and Hyper-IgD Syndrome in an Arabic Kindred
|
Moussa, Taha
|
|
2015
|
35 |
3 |
p. 249-253
|
artikel
|
| 9 |
RAG1 Deficiency May Present Clinically as Selective IgA Deficiency
|
Kato, Tamaki
|
|
2015
|
35 |
3 |
p. 280-288
|
artikel
|
| 10 |
Reduced Frequencies of Polyfunctional CMV-Specific T Cell Responses in Infants with Congenital CMV Infection
|
Gibson, Laura
|
|
2015
|
35 |
3 |
p. 289-301
|
artikel
|
| 11 |
Reduced Frequencies of Polyfunctional CMV-Specific T Cell Responses in Infants with Congenital CMV Infection
|
Gibson, Laura
|
|
|
35 |
3 |
p. 289-301
|
artikel
|
| 12 |
The Duesseldorf Warning Signs for Primary Immunodeficiency: Is it Time to Change the Rules?
|
Lankisch, Petra
|
|
2015
|
35 |
3 |
p. 273-279
|
artikel
|
Tijdschrift beschrijving