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                             16 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Association Between IgA Deficiency & Other Autoimmune Conditions: A Population-Based Matched Cohort Study Ludvigsson, Jonas F.
2014
34 4 p. 444-451
artikel
2 Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation Lougaris, Vassilios
2014
34 4 p. 425-427
artikel
3 Chronic Granulomatous Disease in Morocco: Genetic, Immunological, and Clinical Features of 12 Patients from 10 Kindreds Baba, Laila Ait
2014
34 4 p. 452-458
artikel
4 Correlating Interleukin-12 Stimulated Interferon-γ Production and the Absence of Ectodermal Dysplasia and Anhidrosis (EDA) in Patients with Mutations in NF-κB Essential Modulator (NEMO) Haverkamp, Margje H.
2014
34 4 p. 436-443
artikel
5 Differential microRNA Profile and Post-Transcriptional Regulation Exist in Systemic Lupus Erythematosus Patients with Distinct Autoantibody Specificities Chauhan, Sudhir Kumar
2014
34 4 p. 491-503
artikel
6 Erratum to: Efficacy and Safety of IgPro20, a Subcutaneous Immunoglobulin, in Japanese Patients with Primary Immunodeficiency Diseases Kanegane, Hirokazu
2014
34 4 p. 520
artikel
7 First Report on the Moroccan Registry of Primary Immunodeficiencies: 15 Years of Experience (1998–2012) Bousfiha, A. A.
2014
34 4 p. 459-468
artikel
8 Highly Efficient Neutralization by Plasma Antibodies from Human Immunodeficiency Virus Type-1 Infected Individuals on Antiretroviral Drug Therapy Andrabi, Raiees
2014
34 4 p. 504-513
artikel
9 Highly Efficient Neutralization by Plasma Antibodies from Human Immunodeficiency Virus Type-1 Infected Individuals on Antiretroviral Drug Therapy Andrabi, Raiees

34 4 p. 504-513
artikel
10 ICON: The Early Diagnosis of Congenital Immunodeficiencies Routes, John
2014
34 4 p. 398-424
artikel
11 ICON: The Early Diagnosis of Congenital Immunodeficiencies Routes, John

34 4 p. 398-424
artikel
12 Novel STAT3 Mutation Causing Hyper-IgE Syndrome: Studies of the Clinical Course and Immunopathology Sundin, Mikael
2014
34 4 p. 469-477
artikel
13 Primary Immunodeficiency Disorders in Iran: Update and New Insights from the Third Report of the National Registry Aghamohammadi, Asghar
2014
34 4 p. 478-490
artikel
14 Retrospective Analysis of TREC Based Newborn Screening Results and Clinical Phenotypes in Infants with the 22q11 Deletion Syndrome Lingman Framme, Jenny
2014
34 4 p. 514-519
artikel
15 The Case for Mandatory Newborn Screening for Severe Combined Immunodeficiency (SCID) Gaspar, H. B.
2014
34 4 p. 393-397
artikel
16 USIDNET: A Strategy to Build a Community of Clinical Immunologists Sullivan, Kathleen E.
2014
34 4 p. 428-435
artikel
                             16 gevonden resultaten
 
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