| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Autoantibodies to Variable Heavy (VH) Chain Ig Sequences in Humans Impact the Safety and Clinical Pharmacology of a VH Domain Antibody Antagonist of TNF-α Receptor 1
|
Holland, M. C.
|
|
2013
|
33 |
7 |
p. 1192-1203
|
artikel
|
| 2 |
Autosomal Dominant Anhidrotic Ectodermal Dysplasia with Immunodeficiency Caused by a Novel NFKBIA Mutation, p.Ser36Tyr, Presents with Mild Ectodermal Dysplasia and Non-Infectious Systemic Inflammation
|
Yoshioka, Takakazu
|
|
2013
|
33 |
7 |
p. 1165-1174
|
artikel
|
| 3 |
Collaborating to Improve Quality of Life in Primary Immunodeficiencies: World PI Week, 2013
|
Sorensen, Ricardo
|
|
2013
|
33 |
7 |
p. 1145-1148
|
artikel
|
| 4 |
Colonic Involvement in Celiac Disease and Possible Implications of the Sigmoid Mucosa Organ Culture in its Diagnosis
|
Picarelli, Antonio
|
|
2013
|
33 |
7 |
p. 1250-1256
|
artikel
|
| 5 |
Combined De-Novo Mutation and Non-Random X-Chromosome Inactivation Causing Wiskott-Aldrich Syndrome in a Female with Thrombocytopenia
|
Boonyawat, Boonchai
|
|
2013
|
33 |
7 |
p. 1150-1155
|
artikel
|
| 6 |
Comparative Study of Subcutaneous Versus Intravenous IgG Replacement Therapy in Pediatric Patients with Primary Immunodeficiency Diseases: A Multicenter Study in Argentina
|
Bezrodnik, Liliana
|
|
2013
|
33 |
7 |
p. 1216-1222
|
artikel
|
| 7 |
Erratum to: Molecular Diagnosis of Severe Combined Immunodeficiency—Identification of IL2RG, JAK3, IL7R, DCLRE1C, RAG1, and RAG2 Mutations in a Cohort of Chinese and Southeast Asian Children
|
Lee, Pamela P. W.
|
|
2013
|
33 |
7 |
p. 1269-1270
|
artikel
|
| 8 |
Expression Pattern of Serum Cytokines in Hepatitis B Virus Infected Patients with Persistently Normal Alanine Aminotransferase Levels
|
He, Dengming
|
|
2013
|
33 |
7 |
p. 1240-1249
|
artikel
|
| 9 |
IL-27 is Elevated in Acute Lung Injury and Mediates Inflammation
|
Xu, Fang
|
|
2013
|
33 |
7 |
p. 1257-1268
|
artikel
|
| 10 |
IL-27 is Elevated in Acute Lung Injury and Mediates Inflammation
|
Xu, Fang
|
|
|
33 |
7 |
p. 1257-1268
|
artikel
|
| 11 |
Innate Immune Recognition of Molds and Homology to the Inner Ear Protein, Cochlin, in Patients with Autoimmune Inner Ear Disease
|
Pathak, Shresh
|
|
2013
|
33 |
7 |
p. 1204-1215
|
artikel
|
| 12 |
Lack of Recall Response to Tax in ATL and HAM/TSP Patients But Not in Asymptomatic Carriers of Human T-cell Leukemia Virus Type 1
|
Manuel, Sharrón L.
|
|
2013
|
33 |
7 |
p. 1223-1239
|
artikel
|
| 13 |
Lack of Recall Response to Tax in ATL and HAM/TSP Patients But Not in Asymptomatic Carriers of Human T-cell Leukemia Virus Type 1
|
Manuel, Sharrón L.
|
|
|
33 |
7 |
p. 1223-1239
|
artikel
|
| 14 |
Neurobehavioral Profiles in Individuals with Hyperimmunoglobulin E Syndrome (HIES) and Brain White Matter Hyperintensities
|
Martin, Staci
|
|
2013
|
33 |
7 |
p. 1175-1184
|
artikel
|
| 15 |
Non Invasive Assessment of Lung Disease in Ataxia Telangiectasia by High-Field Magnetic Resonance Imaging
|
Montella, Silvia
|
|
2013
|
33 |
7 |
p. 1185-1191
|
artikel
|
| 16 |
Selective IgA Deficiency: Ruling out Coeliac Disease and Selective Antibody Deficiency to Polysaccharides
|
Della Libera, Ilenia
|
|
2013
|
33 |
7 |
p. 1149
|
artikel
|
| 17 |
The Natural History of Children with Severe Combined Immunodeficiency: Baseline Features of the First Fifty Patients of the Primary Immune Deficiency Treatment Consortium Prospective Study 6901
|
Dvorak, Christopher C.
|
|
|
33 |
7 |
p. 1156-1164
|
artikel
|
| 18 |
The Natural History of Children with Severe Combined Immunodeficiency: Baseline Features of the First Fifty Patients of the Primary Immune Deficiency Treatment Consortium Prospective Study 6901
|
Dvorak, Christopher C.
|
|
2013
|
33 |
7 |
p. 1156-1164
|
artikel
|
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