Hematologically important mutations: X-linked chronic granulomatous disease (third update)

D Roos, DB Kuhns, A Maddalena, J Roesler… - Blood Cells, Molecules …, 2010 - Elsevier
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in
250,000 individuals. The disease is caused by a lack of superoxide production by the …

Bacillus Calmette-Guérin (BCG) complications associated with primary immunodeficiency diseases

S Norouzi, A Aghamohammadi, S Mamishi… - Journal of Infection, 2012 - Elsevier
Primary immunodeficiency diseases (PIDs) are a group of inherited disorders, characterized
by defects of the immune system predisposing individuals to variety of manifestations …

Phagocyte NADPH oxidase, chronic granulomatous disease and mycobacterial infections

C Deffert, J Cachat, KH Krause - Cellular microbiology, 2014 - Wiley Online Library
Infection of humans with M ycobacterium tuberculosis remains frequent and may still lead to
death. After primary infection, the immune system is often able to control M. tuberculosis …

Fourth update on the Iranian National Registry of Primary Immunodeficiencies: integration of molecular diagnosis

H Abolhassani, F Kiaee, M Tavakol… - Journal of clinical …, 2018 - Springer
Background The number of inherited diseases and the spectrum of clinical manifestations of
primary immunodeficiency disorders (PIDs) are ever-expanding. Molecular diagnosis using …

Common infections and target organs associated with chronic granulomatous disease in Iran

E Mortaz, E Azempour, D Mansouri, P Tabarsi… - … Archives of Allergy and …, 2019 - karger.com
Recurrent severe bacterial and fungal infections are characteristic features of the rare
genetic immunodeficiency disorder chronic granulomatous disease (CGD). The disease …

[HTML][HTML] An overview of inflammatory bowel disease: general consideration and genetic screening approach in diagnosis of early onset subsets

S Nemati, S Teimourian - Middle East journal of digestive diseases, 2017 - ncbi.nlm.nih.gov
Inflammatory bowel disease (IBD) is the consequence of an aberrant hemostasis of the
immune cells at the gut mucosal border. Based on clinical manifestation, laboratory tests …

[HTML][HTML] History of primary immunodeficiency diseases in Iran

A Aghamohammadi, M Moin… - Iranian journal of pediatrics, 2010 - ncbi.nlm.nih.gov
Pediatric immunology came into sight in the second half of 20 th century, when pediatricians
and basic immunologists began to give attention to diagnosis and treatment of children with …

Molecular diagnosis of primary immunodeficiency diseases in a developing country: Iran as an example

AH Latif, F Tabassomi, H Abolhassani… - Expert Review of …, 2014 - Taylor & Francis
Primary immunodeficiency diseases (PID) comprise a heterogeneous group of inherited
diseases with a wide spectrum of clinical manifestations and laboratory abnormalities …

Molecular basis of autosomal recessive chronic granulomatous disease in Iran

S Teimourian, M De Boer, D Roos - Journal of clinical immunology, 2010 - Springer
Introduction Chronic granulomatous disease (CGD) is a rare inherited condition resulting
from mutations in the genes that encode the proteins of the NADPH oxidase enzyme in …

Three novel mutations in CYBA among 22 Iranians with Chronic granulomatous disease

M Badalzadeh, S Tajik, MR Fazlollahi… - International journal …, 2017 - Wiley Online Library
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency caused by defect
in one of the components of nicotinamide adenine dinucleotide phosphate (NADPH) …