[HTML][HTML] Introductory Chapter: Introduction on Physiology and Pathology of Immunology

F Rahmani, MR Rahmani, N Rezaei - Physiology and Pathology of …, 2017 - intechopen.com
Dynamic, variable, and diverse overtime and in action, the entire effort of the human body is
to survive. Whether preplanned, ie innate immune reactions, or partly planned, ie adaptive …

Respiratory complications in patients with hyper IgM syndrome

B Moazzami, R Yazdani, G Azizi, F Kiaei… - Journal of clinical …, 2019 - Springer
Abstract Purpose Hyper Immunoglobulin M (HIgM) syndrome is a heterogeneous group of
primary immunodeficiency disorders, characterized by recurrent infections and associated …

The first case report of complement component 7 deficiency in Qatar and a 10-year follow-up

SM Khalil, S Aqel, DS Mudawi, H Mobayed… - Frontiers in …, 2023 - frontiersin.org
Introduction Neisseria meningitidis is a significant cause of bacterial meningitis and
septicemia worldwide. Recurrent Neisseria meningitidis is frequently associated with …

Clearing vaccine-derived poliovirus infection following hematopoietic stem cell transplantation: a case report and review of literature

M Shaghaghi, M Irannejad, H Abolhassani… - Journal of Clinical …, 2018 - Springer
The use of oral poliovirus vaccine in a worldwide scale has led to a 99.9% decrease in
annual incidence of wild-type poliomyelitis and the eradication of serotype 2 poliovirus …

Gene mutations responsible for primary immunodeficiency disorders: a report from the first primary immunodeficiency biobank in Iran

S Sheikhbahaei, R Sherkat, D Roos, M Yaran… - Allergy, Asthma & …, 2016 - Springer
Background Primary immunodeficiency (PID) is a heterogeneous group of inheritable
genetic disorders with increased susceptibility to infections, autoimmunity, uncontrolled …

Primary immunodeficiency diseases in Northern Iran

I Mohammadzadeh, B Moazzami, J Ghaffari… - Allergologia et …, 2017 - Elsevier
Introduction Primary immunodeficiency diseases (PID) are a heterogeneous group of
inherited disorders, characterised by recurrent severe infections, autoimmunity and …

Role of apoptosis in the pathogenesis of common variable immunodeficiency (CVID)

M Ganjalikhani-Hakemi, R Yazdani… - … Metabolic & Immune …, 2017 - ingentaconnect.com
Background: Common variable immunodeficiency (CVID) is a heterogeneous immune
deficiency characterized by hypogammaglobulinemia. Since B cell maturation and …

Sinopulmonary complications in subjects with primary immunodeficiency

A Owayed, W Al-Herz - Respiratory care, 2016 - rc.rcjournal.com
BACKGROUND: The aim of this work was to describe the frequency and spectrum of
sinopulmonary complications among subjects with primary immunodeficiency disorders …

A comparison of clinical and immunologic phenotypes in familial and sporadic forms of common variable immunodeficiency

A Valizadeh, R Yazdani, G Azizi… - Scandinavian …, 2017 - Wiley Online Library
Common variable immunodeficiency (CVID) is the most frequent symptomatic primary
immunodeficiency disease, and its prevalence varies significantly among different …

G2-lymphocyte chromosomal radiosensitivity in patients with LPS responsive beige-like anchor protein (LRBA) deficiency

H Mozdarani, F Kiaee, S Fekrvand, G Azizi… - … Journal of Radiation …, 2019 - Taylor & Francis
Lipopolysaccharide-responsive, beige-like anchor protein (LRBA) deficiency is an
autosomal recessive primary immunodeficiency disease characterized by a CVID-like …