nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An Impaired Inflammatory Cytokine Response to Gram-Negative LPS in Human Neonates is Associated with the Defective TLR-Mediated Signaling Pathway
|
Li, Yi Ping |
|
2015 |
35 |
2 |
p. 218-226 |
artikel |
2 |
A Note from the Editor-in-Chief, Deputy Editor, and Managing Editor
|
Bonagura, Vincent R. |
|
2015 |
35 |
2 |
p. 97 |
artikel |
3 |
Antibody Levels to Bordetella pertussis and Neisseria meningitidis in Immunodeficient Patients Receiving Immunoglobulin Replacement Therapy
|
Adam, Etai |
|
2015 |
35 |
2 |
p. 213-217 |
artikel |
4 |
Are Patients with X-Linked Agammaglobulinemia at Increased Risk of Developing Acute Lymphoblastic Leukemia?
|
Conley, Mary Ellen |
|
2015 |
35 |
2 |
p. 98-99 |
artikel |
5 |
Combined Immunodeficiency Due to MALT1 Mutations, Treated by Hematopoietic Cell Transplantation
|
Punwani, Divya |
|
2015 |
35 |
2 |
p. 135-146 |
artikel |
6 |
Coronin-1A: Immune Deficiency in Humans and Mice
|
Punwani, Divya |
|
2015 |
35 |
2 |
p. 100-107 |
artikel |
7 |
DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
|
Aydin, Susanne E. |
|
2015 |
35 |
2 |
p. 189-198 |
artikel |
8 |
Fertility, Pregnancies and Outcomes Reported by Females with Common Variable Immune Deficiency and Hypogammaglobulinemia: Results from an Internet-Based Survey
|
Gundlapalli, Adi V. |
|
2015 |
35 |
2 |
p. 125-134 |
artikel |
9 |
Identification of a Novel Mutation in MAGT1 and Progressive Multifocal Leucoencephalopathy in a 58-Year-Old Man with XMEN Disease
|
Dhalla, Fatima |
|
2014 |
35 |
2 |
p. 112-118 |
artikel |
10 |
Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders
|
Buchbinder, David |
|
2014 |
35 |
2 |
p. 119-124 |
artikel |
11 |
IgA Deficiency and Risk of Cancer: A Population-Based Matched Cohort Study
|
Ludvigsson, Jonas F. |
|
2015 |
35 |
2 |
p. 182-188 |
artikel |
12 |
Infectious and Immunologic Phenotype of MECP2 Duplication Syndrome
|
Bauer, Michael |
|
2015 |
35 |
2 |
p. 168-181 |
artikel |
13 |
Infectious and Immunologic Phenotype of MECP2 Duplication Syndrome
|
Bauer, Michael |
|
|
35 |
2 |
p. 168-181 |
artikel |
14 |
Modulatory Role of Intravenous Gammaglobulin (IgIV) on the in vitro Antibody Response to a Pneumococcal Polysaccharide Antigen
|
Leiva, Lily E. |
|
2014 |
35 |
2 |
p. 206-212 |
artikel |
15 |
Modulatory Role of Intravenous Gammaglobulin (IgIV) on the in vitro Antibody Response to a Pneumococcal Polysaccharide Antigen
|
Leiva, Lily E. |
|
|
35 |
2 |
p. 206-212 |
artikel |
16 |
Monocyte/macrophage-Specific NADPH Oxidase Contributes to Antimicrobial Host Defense in X-CGD
|
Okura, Yuka |
|
2015 |
35 |
2 |
p. 158-167 |
artikel |
17 |
Nijmegen Breakage Syndrome Detected by Newborn Screening for T Cell Receptor Excision Circles (TRECs)
|
Patel, Jay P. |
|
2015 |
35 |
2 |
p. 227-233 |
artikel |
18 |
Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe
|
Turley, A. J. |
|
2015 |
35 |
2 |
p. 199-205 |
artikel |
19 |
Variable Phenotype of Severe Immunodeficiencies Associated with RMRP Gene Mutations
|
Ip, Winnie |
|
2015 |
35 |
2 |
p. 147-157 |
artikel |
20 |
X-Linked Agammaglobulinemia Associated with B-Precursor Acute Lymphoblastic Leukemia
|
Hoshino, Akihiro |
|
2015 |
35 |
2 |
p. 108-111 |
artikel |