[HTML][HTML] Evaluation of miR-210 expression in common variable immunodeficiency: patients with unsolved genetic defect
Background: Common variable immunodeficiency (CVID) is one of the most prevalent forms
of primary immunodeficiency diseases (PID). CVID is characterized by failure in the final …
of primary immunodeficiency diseases (PID). CVID is characterized by failure in the final …
[PDF][PDF] The spectrum of inborn errors of immunity: a single tertiary center retrospective study in Alborz, Iran
SE Rasouli, M Tavakol, H Sadri… - Eur Ann Allergy Clin …, 2021 - eurannallergyimm.com
Background. Inborn errors of immunity (IEIs) are a group of heterogeneous disorders with
inherited faults in the immune system that increase susceptibility to infections, malignancies …
inherited faults in the immune system that increase susceptibility to infections, malignancies …
Cernunnos defect in an Iranian patient with T− B+ NK+ severe combined immunodeficiency: A case report and review of the literature
Abstract Background Defective Cernunnos gene in nonhomologous end‐joining (NHEJ)
pathway of the DNA repair is responsible for radiosensitive severe combined …
pathway of the DNA repair is responsible for radiosensitive severe combined …
Evaluation of patients with primary immunodeficiency associated with Bacille Calmette-Guerin (BCG)-vaccine-derived complications
Abstract Background Bacille Calmette-Guerin (BCG) vaccination has a great impact on the
prevention of severe complications of tuberculosis. However, in patients with primary …
prevention of severe complications of tuberculosis. However, in patients with primary …
Algerian Registry for Inborn Errors of Immunity in Children: Report of 887 Children (1985–2021)
Introduction Inborn errors of immunity (IEI) represent a heterogeneous large group of genetic
disorders characterized by susceptibility of affected individuals to recurrent infections …
disorders characterized by susceptibility of affected individuals to recurrent infections …
Evaluation of respiratory complications in patients with X‐linked and autosomal recessive agammaglobulinemia
Background Congenital agammaglobulinemia is the first primary immunodeficiency disorder
characterized by a defect in B lymphocyte development and subsequently decreased …
characterized by a defect in B lymphocyte development and subsequently decreased …
Evaluation of microRNA-125b-5p and transcription factors BLIMP1 and IRF4 expression in unsolved common variable immunodeficiency patients
Common variable immunodeficiency (CVID) is the most prevalent form of symptomatic
primary humoral immunodeficiencies characterized by failure in the final differentiation of B …
primary humoral immunodeficiencies characterized by failure in the final differentiation of B …
Adverse reactions in a large cohort of patients with inborn errors of immunity receiving intravenous immunoglobulin
H Esmaeilzadeh, A Askarisarvestani, N Hosseini… - Clinical …, 2021 - Elsevier
Abstract Background Intravenous immunoglobulins (IVIg) are the major treatment in inborn
errors of immunity (IEI) disorders; However, IVIg infusions show some adverse effects. We …
errors of immunity (IEI) disorders; However, IVIg infusions show some adverse effects. We …
The prevalence of selective and partial immunoglobulin a deficiency in patients with autoimmune polyendocrinopathy
Background Autoimmune disorders are reported as presenting signs in patients with
immunoglobulin A (IgA) deficiency. Herein, we aim to evaluate serum IgA among patients …
immunoglobulin A (IgA) deficiency. Herein, we aim to evaluate serum IgA among patients …
Common presentations and diagnostic approaches
N Rezaei, E de Vries, E Gambineri… - Stiehm's immune …, 2014 - Elsevier
Primary immune deficiencies are a heterogeneous group of inherited disorders caused by
specific gene mutations affecting the immune system and leading to various clinical …
specific gene mutations affecting the immune system and leading to various clinical …