nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF)
|
Rechavi, Erez |
|
2016 |
36 |
8 |
p. 801-809 |
artikel |
2 |
Asthma and Hypogammaglobulinemia: an Asthma Phenotype with Low Type 2 Inflammation
|
Dupin, Clairelyne |
|
2016 |
36 |
8 |
p. 810-817 |
artikel |
3 |
Ataxia telangiectasia associated with nodular regenerative hyperplasia
|
Milligan, Ki L. |
|
2016 |
36 |
8 |
p. 739-742 |
artikel |
4 |
Autoimmune and Inflammatory Manifestations in 247 Patients with Primary Immunodeficiency—a Report from the Slovenian National Registry
|
Blazina, Štefan |
|
2016 |
36 |
8 |
p. 764-773 |
artikel |
5 |
Clinical, Immunological, and Molecular Findings of Patients with p47phox Defect Chronic Granulomatous Disease (CGD) in Indian Families
|
Kulkarni, Manasi |
|
2016 |
36 |
8 |
p. 774-784 |
artikel |
6 |
CTP Synthase 1 Deficiency in Successfully Transplanted Siblings with Combined Immune Deficiency and Chronic Active EBV Infection
|
Kucuk, Zeynep Yesim |
|
2016 |
36 |
8 |
p. 750-753 |
artikel |
7 |
Familial Chronic Granulomatous Disease Affecting Three Siblings and Causing Recurrent Tuberculosis
|
Pereira, Noella Maria Delia |
|
2016 |
36 |
8 |
p. 743-746 |
artikel |
8 |
“How I manage” IgG4-Related Disease
|
Della-Torre, Emanuel |
|
2016 |
36 |
8 |
p. 754-763 |
artikel |
9 |
Neurologic Complications of Common Variable Immunodeficiency
|
Nguyen, Jenna Thuc-Uyen |
|
2016 |
36 |
8 |
p. 793-800 |
artikel |
10 |
Primary Immunodeficiency Diseases in Oman: 10-Year Experience in a Tertiary Care Hospital
|
Al-Tamemi, Salem |
|
2016 |
36 |
8 |
p. 785-792 |
artikel |
11 |
The Importance of Measuring IL10 Levels in Patients with Suspected IL10/IL10R Defects
|
LaBarba, Susanne |
|
2016 |
36 |
8 |
p. 747-749 |
artikel |