no |
title |
author |
magazine |
year |
volume |
issue |
page(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 |
article |
2 |
2018 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference
|
|
|
2018 |
38 |
3 |
p. 330-444 |
article |
3 |
2018 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference
|
|
|
|
38 |
3 |
p. 330-444 |
article |
4 |
Combined Immunodeficiency with Ring Chromosome 21
|
Norman, Melissa |
|
2018 |
38 |
3 |
p. 251-256 |
article |
5 |
Complications Associated with Underweight Primary Immunodeficiency Patients: Prevalence and Associations Within the USIDNET Registry
|
Ruffner, Melanie A. |
|
2018 |
38 |
3 |
p. 283-293 |
article |
6 |
Droplet Digital PCR-Based Chimerism Analysis for Primary Immunodeficiency Diseases
|
Okano, Tsubasa |
|
2018 |
38 |
3 |
p. 300-306 |
article |
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 |
article |
8 |
Francisella philomiragia: Think of Chronic Granulomatous Disease
|
Robles-Marhuenda, Angel |
|
2018 |
38 |
3 |
p. 257-259 |
article |
9 |
From Ignác Semmelweis to Primary Immunodeficiencies: a Bicentenary Commemoration
|
Maródi, László |
|
2018 |
38 |
3 |
p. 247-250 |
article |
10 |
Hemophagocytic Lymphohistiocytosis in Loeys-Dietz Syndrome
|
Biggin, Andrew |
|
2018 |
38 |
3 |
p. 234-236 |
article |
11 |
Immunoglobulin E—an Innocent Bystander in Host Defense?
|
Zhang, Qian |
|
2018 |
38 |
3 |
p. 223-224 |
article |
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 |
article |
13 |
Low Serum IgE Is a Sensitive and Specific Marker for Common Variable Immunodeficiency (CVID)
|
Lawrence, Monica G. |
|
2018 |
38 |
3 |
p. 225-233 |
article |
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 |
article |
15 |
Novel Mutation in CECR1 Leads to Deficiency of ADA2 with Associated Neutropenia
|
Cipe, Funda Erol |
|
2018 |
38 |
3 |
p. 273-277 |
article |
16 |
Use of Genetic Testing for Primary Immunodeficiency Patients
|
Heimall, Jennifer R. |
|
2018 |
38 |
3 |
p. 320-329 |
article |
17 |
Utility of DNA, RNA, Protein, and Functional Approaches to Solve Cryptic Immunodeficiencies
|
Cousin, Margot A. |
|
2018 |
38 |
3 |
p. 307-319 |
article |