Explanipedia

Co-Robopv: Cooperative Aerial Robot System for Photovoltaic Power Plant Inspection Based on Reinforcement Learning Open

Asghar Aghamohammadi, Sayyed Majid Esmailifar, Mohammad Kolahi, Amir Mohammad Moradi Sizkouhi, Mohammadreza Aghaei · 2025

Autonomous Intelligent Monitoring of Photovoltaic Systems: An In-depth Multidisciplinary Review Open

Mohammadreza Aghaei, Mohammad Kolahi, Amir Nedaei, Venkatesh N.S., Sayyed Majid Esmailifar , et al. · 2024

This study presents a comprehensive multidisciplinary review of autonomous monitoring and analysis of large-scale photovoltaic (PV) power plants using enabling technologies, namely artificial intelligence, machine learning, deep learning, …

Demographic, Clinical, and Immunological features in Combined Immunodeficiency Patients with Pulmonary Complications: A Retrospective Multicenter Study from Iran Open

Ghamartaj Khanbabaee, Matin Pourghasem, Mahnaz Jamee, Seyed Ahmad Tabatabaii, Mitra Khalili , et al. · 2023

Background: Combined immunodeficiency (CID) is characterized by profound defects in the development and function of both B and T cells. We aimed to investigate clinical and immunological phenotype in CID patients with and without pulmonary…

B cells and T cells abnormalities in patients with selective IgA deficiency Open

Yasser Bagheri, Tannaz Moeini Shad, Shideh Namazi, Farzaneh Tofighi Zavareh, Gholamreza Azizi , et al. · 2023

Background Selective IgA deficiency (SIgAD) is the most prevalent inborn errors of immunity with almost unknown etiology. This study aimed to investigate the clinical diagnostic and prognostic values of lymphocyte subsets and function in s…

Analysis of Lymphocyte and Clinical Profile in Nonmonogenic Common Variable Immunodeficiency Patients With and Without Class Switch Recombination Defect Open

Farzaneh Tofighi Zavareh, Abbas Mirshafiey, Reza Yazdani, Abbasali Keshtkar, Hassan Abolhassani , et al. · 2023

Table S1.Demographic features of 30 genetically unsolved CVID patients with (

Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients Open

Christoph B. Geier, Maryssa Ellison, Rachel Cruz, Sumit Pawar, Alexander Leiss-Piller , et al. · 2022

Atypical Ataxia Presentation in Variant Ataxia Telangiectasia: Iranian Case-Series and Review of the Literature Open

Tannaz Moeini Shad, Reza Yazdani, Parisa Amirifar, Samaneh Delavari, Marzieh Heidarzadeh Arani , et al. · 2022

Ataxia-telangiectasia (AT) is a rare autosomal recessive neurodegenerative multisystem disorder. A minority of AT patients can present late-onset atypical presentations due to unknown mechanisms. The demographic, clinical, immunological an…

Evaluation of MicroRNA-125b-5p and Transcription Factors BLIMP1 and IRF4 Expression in Unsolved Common Variable Immunodeficiency Patients Open

Zahra Esfahani, Reza Yazdani, Sepideh Shahkarami, Fateme Babaha, Hassan Abolhassani , et al. · 2021

Common variable immunodeficiency (CVID) is the most prevalent form of symptomatic primary humoral immunodeficiencies characterized by failure in the final differentiation of B lymphocytes. The majority of CVID cases have no identified gene…

T Cell Repertoire Abnormality in Immunodeficiency Patients with DNA Repair and Methylation Defects Open

Mingyan Fang, Zheng Su, Hassan Abolhassani, Wei Zhang, Chongyi Jiang , et al. · 2021

Both DNA damage response and methylation play a crucial role in antigen receptor recombination by creating a diverse repertoire in developing lymphocytes, but how their defects relate to T cell repertoire and phenotypic heterogeneity of im…

Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia Patients Open

Parisa Amirifar, Mahya Mehrmohamadi, Mohammad Reza Ranjouri, Seyed Mohammad Akrami, Nima Rezaei , et al. · 2021

Demographic, Clinical, and Immunological Features in Combined Immunodeficiency Patients with and Without Pulmonary Complications: A Retrospective Multicenter Study from Iran Open

Ghamartaj Khanbabaee, Matin Pourghasem, Mahnaz Jamee, Seyed Ahmad Tabatabaii, Mitra Khalili , et al. · 2021

Purpose: Combined immunodeficiency (CID) is characterized by profound defects in the development and function of both B and T cells. We aimed to investigate clinical and immunological phenotype in CID patients with and without pulmonary co…

Known and potential molecules associated with altered B cell development leading to predominantly antibody deficiencies Open

Parisa Amirifar, Reza Yazdani, Gholamreza Azizi, Mohammad Reza Ranjouri, Anne Durandy , et al. · 2021

Predominantly antibody deficiencies (PADs) encompass a heterogeneous group of disorders characterized by low immunoglobulin serum levels in the presence or absence of peripheral B cells. Clinical presentation of affected patients may inclu…

Author response for "Known and Potential Molecules Associated with Altered B cell Development Leading to Predominantly Antibody Deficiencies" Open

Parisa Amirifar, Reza Yazdani, Gholamreza Azizi, Mohammad Reza Ranjouri, Anne Durandy , et al. · 2021

Consensus Middle East and North Africa Registry on Inborn Errors of Immunity Open

Asghar Aghamohammadi, Nima Rezaei, Reza Yazdani, Samaneh Delavari, Necil Kütükçüler , et al. · 2021

International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome Open

Dimana Dimitrova, Zohreh Nademi, Maria Elena Maccari, Stephan Ehl, Gülbû Uzel , et al. · 2021

Author response for "Clinical, immunological, and genetic features in 780 patients with autoimmune lymphoproliferative syndrome (ALPS) and ALPS-like diseases: A systematic review" Open

Nasim Hafezi, Majid Zaki‐Dizaji, Matineh Nirouei, Gelayol Asadi, Niusha Sharifinejad , et al. · 2021

Evaluation of miR-210 expression in common variable immunodeficiency: patients with unsolved genetic defect Open

Fateme Babaha, Reza Yazdani, Sepideh Shahkarami, Zahra Esfahani, Hassan Abolhahassani , et al. · 2021

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 differentiation of B lymphocytes and impaired antibody product…

Author response for "Clinical, immunological, and genetic features in 780 patients with autoimmune lymphoproliferative syndrome (ALPS) and ALPS-like diseases: A systematic review" Open

Nasim Hafezi, Majid Zaki‐Dizaji, Matineh Nirouei, Gelayol Asadi, Niusha Sharifinejad , et al. · 2021

Author response for "Autoimmune Manifestations among Patients with Monogenic Inborn Errors of Immunity" Open

Gholamreza Azizi, Marzieh Tavakol, Reza Yazdani, Samaneh Delavari, Tannaz Moeini Shad , et al. · 2021

Primary Immunodeficiency Diseases in Iran: Past, Present and Future Open

Asghar Aghamohammadi, Hassan Abolhassani, Nima Rezaei · 2021

Clinical immunology and its subset topics are rather newly emerging medical fields in Iran as well as other developing countries. Primary immunodeficiency diagnosis and treatment were revolutionized in the late 1970s; a period of time that…

B cells and T cells Abnormalities in Patients with Selective IgA Deficiency Open

Yasser Bagheri, Tannaz Moeini Shad, Shideh Namazi, Gholamreza Azizi, Ali Hosseini , et al. · 2021

Background: Selective IgA deficiency (SIgAD) is the most prevalent primary immunodeficiency with almost unknown etiology. This study aimed to investigate the clinical diagnostic and prognostic values of lymphocytes subsets and function in …

Severe Ophthalmic Involvement in Hyperimmunoglobulin E Syndrome; a Potentially Blinding Disease Open

Masoumeh Mohebbi, Hossein Ghahvehchian, Asghar Aghamohammadi, Hassan Hashemi · 2021

Objective: To describe clinical and flow cytometry findings of an unusual case of hyper immunoglobulin E syndrome with severe ophthalmic involvements. Method : A Case report. Report: A 13-year-old boy was reported with infectious dermatiti…

Lymphocytes subsets in correlation with clinical profile in CVID patients without monogenic defects Open

Farzaneh Tofighi Zavareh, Abbas Mirshafiey, Reza Yazdani, Abbasali Keshtkar, Hassan Abolhassani , et al. · 2021

Objectives: Common variable immunodeficiency (CVID) patients experience clinical manifestations rather than recurrent respiratory infections including autoimmunity, enteropathy, and lymphoproliferation. We evaluated the correlation …

Somatic reversion of pathogenic DOCK8 variants alters lymphocyte differentiation and function to effectively cure DOCK8 deficiency Open

Bethany Pillay, Mathieu Fusaro, Paul Gray, Aaron L. Statham, Leslie Burnett , et al. · 2020

Inborn errors of immunity cause monogenic immune dysregulatory conditions such as severe and recurrent pathogen infection, inflammation, allergy, and malignancy. Somatic reversion refers to the spontaneous repair of a pathogenic germline g…

The spectrum of ATM gene mutations in Iranian patients with ataxia-telangiectasia Open

Parisa Amirifar, Mohammad Reza Ranjouri, Salar Pashangzadeh, Martin F. Lavin, Reza Yazdani , et al. · 2020

Background: Ataxia-telangiectasia (A-T) is a rare genetic disorder characterized by a distinct range of clinical manifestations, including progressive ataxia, immunodeficiency, and radiosensitivity. Methods: Clinical data, laboratory resul…

Clinical complications and their management in a child with ataxia‐telangiectasia (A‐T): A case report study Open

Marzieh Heidarzadeh Arani, Reza Arefnezhad, Javad Fathgharib, Asghar Aghamohammadi, Hossein Motedayyen · 2020

Ataxia‐telangiectasia (A‐T) is known as an uncommon autosomal recessive disorder associated with recurrent infections and other clinical complications. The management of its complications can improve life quality of patients.

Evaluation of Expression of LRBA and CTLA-4 Proteins in Common Variable Immunodeficiency Patients Open

Fereshte Salami, Saba Fekrvand, Reza Yazdani, Sepideh Shahkarami, Gholamreza Azizi , et al. · 2020

Common variable immunodeficiency (CVID) is a primary immunodeficiency disease with a heterogeneous genetic background. Lipopolysaccharide-responsive beige-like anchor (LRBA), as well as cytotoxic T-lymphocyte-associated protein 4 (CTLA-4),…

Evaluation of patients with primary immunodeficiency associated with Bacille Calmette-Guerin (BCG)-vaccine-derived complications Open

Mahsa Sohani, S Habibi, Samaneh Delavari, Sepideh Shahkarami, Reza Yazdani , et al. · 2020

The high rate of undiagnosed PIDs predisposes individuals to a high risk of severe side effects as a result of BCG vaccination, as well as infants that are less than one month of age. Therefore, there is a need for early screening and diag…

Country Quarantine During COVID-19: Critical or Not? Open

Noosha Samieefar, Reza Yari Boroujeni, Mahnaz Jamee, Melika Lotfi, Mohammad Rasoul Golabchi , et al. · 2020

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Infectious Complications Reporting in Common Variable Immunodeficiency: A Systematic Review and Meta-analysis Open

Hamed Zainaldain, Fatema Sadaat Rizvi, Hosein Rafiemanesh, Mahla Alizadeh, Mahnaz Jamee , et al. · 2020

OBJECTIVES: Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by hypogammaglobulinemia and increased susceptibility to recurrent infections. METHODS: We searched PubMed, Web of Science, and Scopus databases …

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