nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Diarrhea as sole presentation of Good's syndrome mimicking Crohn's disease
|
Mancuso, Andrea |
|
2013 |
147 |
1 |
p. 9-10 |
artikel |
2 |
Editorial Board
|
|
|
2013 |
147 |
1 |
p. IFC |
artikel |
3 |
Elevated serum IL-22 levels correlate with chemoresistant condition of colorectal cancer
|
Wu, Tingyu |
|
2013 |
147 |
1 |
p. 38-39 |
artikel |
4 |
Eosinophil recruitment to nasal nerves after allergen challenge in allergic rhinitis
|
Thornton, Margaret A. |
|
2013 |
147 |
1 |
p. 50-57 |
artikel |
5 |
Erratum to “High-dose intravenous immunoglobulin does not reduce the numbers of circulating CD14+CD16++ monocytes in patients with inflammatory disorders” [Clin. Immunol. 145 (2012) 11–12]
|
Tjon, Angela S.W. |
|
2013 |
147 |
1 |
p. 69 |
artikel |
6 |
Familial Mediterranean fever mutations in a patient with recurrent episodes of acute respiratory distress syndrome
|
Arai, Yasuyuki |
|
2013 |
147 |
1 |
p. 58-60 |
artikel |
7 |
Gluten-sensitive enteropathy coincides with decreased capability of intestinal T cells to secrete IL-17 and IL-22 in a macaque model for celiac disease
|
Xu, Huanbin |
|
2013 |
147 |
1 |
p. 40-49 |
artikel |
8 |
Hypoxia potentiates allergen induction of HIF-1α, chemokines, airway inflammation, TGF-β1, and airway remodeling in a mouse model
|
Baek, Kwang Je |
|
2013 |
147 |
1 |
p. 27-37 |
artikel |
9 |
Predictive immunomonitoring — The COST ENTIRE initiative
|
Popadic, Dusan |
|
2013 |
147 |
1 |
p. 23-26 |
artikel |
10 |
Protein kinase C delta is a substrate of tissue transglutaminase and a novel autoantigen in coeliac disease
|
Byrne, Greg |
|
2013 |
147 |
1 |
p. 1-8 |
artikel |
11 |
Signature MicroRNA expression patterns identified in humans with 22q11.2 deletion/DiGeorge syndrome
|
de la Morena, M. Teresa |
|
2013 |
147 |
1 |
p. 11-22 |
artikel |
12 |
Somatic loss of heterozygosity, but not haploinsufficiency alone, leads to full-blown autoimmune lymphoproliferative syndrome in 1 of 12 family members with FAS start codon mutation
|
Hauck, Fabian |
|
2013 |
147 |
1 |
p. 61-68 |
artikel |