Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: a longitudinal study

G Azizi, H Abolhassani, SA Mahdaviani… - Pediatric Allergy and …, 2017 - Wiley Online Library
Background LPS‐responsive beige‐like anchor protein (LRBA) deficiency is a combined
immunodeficiency caused by mutation in LRBA gene. The patients have a variety of clinical …

The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency

L Gámez-Díaz, D August, P Stepensky… - Journal of Allergy and …, 2016 - Elsevier
Background LPS-responsive beige-like anchor protein (LRBA) deficiency is a primary
immunodeficiency caused by biallelic mutations in LRBA that abolish LRBA protein …

Clinical, immunologic, and molecular spectrum of patients with LPS-responsive beige-like anchor protein deficiency: a systematic review

S Habibi, M Zaki-Dizaji, H Rafiemanesh, B Lo… - The Journal of Allergy …, 2019 - Elsevier
Background LPS-responsive beige-like anchor protein (LRBA) deficiency is a primary
immunodeficiency and immune dysregulation syndrome caused by biallelic mutations in the …

[HTML][HTML] Multiple presentations of LRBA deficiency: a single-center experience

S Kostel Bal, S Haskologlu, NK Serwas… - Journal of clinical …, 2017 - Springer
Introduction LPS-responsive beige-like anchor protein (LRBA) deficiency is a primary
immunodeficiency categorized as common variable immunodeficiency associated with …

[HTML][HTML] Respiratory manifestations in LPS-responsive beige-like anchor (LRBA) protein-deficient patients

O Shamriz, B Shadur, A NaserEddin, I Zaidman… - European journal of …, 2018 - Springer
Abstract Lipopolysaccharide (LPS)-responsive beige-like anchor (LRBA) protein deficiency
is a rare syndrome of primary immune deficiency and immune dysregulation. In this study …

Clinical phenotypes and immunological characteristics of 18 Egyptian LRBA deficiency patients

S Meshaal, R El Hawary, R Adel, D Abd Elaziz… - Journal of Clinical …, 2020 - Springer
LPS-responsive beige-like anchor (LRBA) deficiency is an autosomal recessive primary
immunodeficiency disorder, OMIM (# 614700). LRBA deficiency patients suffer from variable …

Abatacept as a long-term targeted therapy for LRBA deficiency

A Kiykim, I Ogulur, E Dursun, LM Charbonnier… - The Journal of Allergy …, 2019 - Elsevier
Background LPS-responsive beige-like anchor (LRBA) deficiency presents with
susceptibility to infections, autoimmunity, and lymphoproliferation. The long-term efficacy of …

Polyautoimmunity in patients with LPS-responsive beige-like anchor (LRBA) deficiency

G Azizi, H Abolhassani, M Zaki-Dizaji… - Immunological …, 2018 - Taylor & Francis
Background: Polyautoimmunity is defined as the presence of more than one autoimmune
disorder in a single patient. Lipopolysaccharide (LPS)-responsive beige-like anchor (LRBA) …

The imbalance of circulating T helper subsets and regulatory T cells in patients with LRBA deficiency: correlation with disease severity

G Azizi, A Mirshafiey, H Abolhassani… - Journal of Cellular …, 2018 - Wiley Online Library
Lipopolysaccharides responsive beige‐like anchor protein (LRBA) deficiency is a clinically
variable primary immunodeficiency (PID) syndrome caused by loss‐of‐function mutations in …

Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation

MG Seidel, K Böhm, F Dogu, A Worth… - Journal of Allergy and …, 2018 - jacionline.org
LPS-responsive beige-like anchor protein (LRBA) deficiency is a severe primary
immunodeficiency with a variable clinical phenotype, including features overlapping with …