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                             11 gevonden resultaten
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
                             11 gevonden resultaten
 
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