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                             17 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Cohort of 169 Chronic Granulomatous Disease Patients Exposed to BCG Vaccination: a Retrospective Study from a Single Center in Shanghai, China (2004–2017) Zhou, Qinhua
2018
38 3 p. 260-272
artikel
2 2018 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference 2018
38 3 p. 330-444
artikel
3 2018 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference
38 3 p. 330-444
artikel
4 Combined Immunodeficiency with Ring Chromosome 21 Norman, Melissa
2018
38 3 p. 251-256
artikel
5 Complications Associated with Underweight Primary Immunodeficiency Patients: Prevalence and Associations Within the USIDNET Registry Ruffner, Melanie A.
2018
38 3 p. 283-293
artikel
6 Droplet Digital PCR-Based Chimerism Analysis for Primary Immunodeficiency Diseases Okano, Tsubasa
2018
38 3 p. 300-306
artikel
7 First Analysis of SERPING1 Gene in Patients with Hereditary Angioedema in Colombia Reveals Two Genotypic Variants in a Highly Symptomatic Individual Rodríguez, Jairo A.
2018
38 3 p. 294-299
artikel
8 Francisella philomiragia: Think of Chronic Granulomatous Disease Robles-Marhuenda, Angel
2018
38 3 p. 257-259
artikel
9 From Ignác Semmelweis to Primary Immunodeficiencies: a Bicentenary Commemoration Maródi, László
2018
38 3 p. 247-250
artikel
10 Hemophagocytic Lymphohistiocytosis in Loeys-Dietz Syndrome Biggin, Andrew
2018
38 3 p. 234-236
artikel
11 Immunoglobulin E—an Innocent Bystander in Host Defense? Zhang, Qian
2018
38 3 p. 223-224
artikel
12 Immunologist’s Perspectives on Assessment and Management of Lung Disease in CVID: a Survey of the Membership of the Clinical Immunology Society and the European Society for Immunodeficiencies Akhter, Javeed
2018
38 3 p. 237-246
artikel
13 Low Serum IgE Is a Sensitive and Specific Marker for Common Variable Immunodeficiency (CVID) Lawrence, Monica G.
2018
38 3 p. 225-233
artikel
14 Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia Alodayani, Abdulrahman N.
2018
38 3 p. 278-282
artikel
15 Novel Mutation in CECR1 Leads to Deficiency of ADA2 with Associated Neutropenia Cipe, Funda Erol
2018
38 3 p. 273-277
artikel
16 Use of Genetic Testing for Primary Immunodeficiency Patients Heimall, Jennifer R.
2018
38 3 p. 320-329
artikel
17 Utility of DNA, RNA, Protein, and Functional Approaches to Solve Cryptic Immunodeficiencies Cousin, Margot A.
2018
38 3 p. 307-319
artikel
                             17 gevonden resultaten
 
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