Samaneh Delavari
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Explore the profile of Samaneh Delavari including associated specialties, affiliations and a list of published articles.
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39
Citations
295
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Recent Articles
1.
Salami F, Shad T, Fathi N, Mojtahedi H, Esmaeili M, Shahkarami S, et al.
J Clin Immunol
. 2025 Jan;
45(1):67.
PMID: 39853455
Background: Ataxia telangiectasia mutated (ATM) kinase plays a critical role in DNA double-strand break (DSB) repair. Ataxia telangiectasia (A-T) patients exhibit abnormalities in immunoglobulin isotype expression and class switch recombination...
2.
Delavari S, Rasouli S, Fekrvand S, Chavoshzade Z, Mahdaviani S, Shirmast P, et al.
Clin Immunol
. 2024 Jan;
259:109896.
PMID: 38184287
Background: Inborn errors of immunity (IEI) are a diverse range of genetic immune system illnesses affecting the innate and/or adaptive immune systems. Variable expressivity and incomplete penetrance have been reported...
3.
Bayegi S, Hamidieh A, Behfar M, Saghazadeh A, Bozorgmehr M, Tajik N, et al.
Endocr Metab Immune Disord Drug Targets
. 2023 Aug;
24(2):265-272.
PMID: 37526450
Background: Congenital amegakaryocytic thrombocytopenia (CAMT) is a bone marrow failure syndrome with autosomal recessive inheritance characterized by the lack of megakaryocytes and thrombocytopenia. The cause of the disease is a...
4.
Bayegi S, Hamidieh A, Behfar M, Bozorgmehr M, Saghazadeh A, Tajik N, et al.
Immunol Lett
. 2023 Jul;
261:25-36.
PMID: 37474024
Background: The reconstitution of different T-cell subsets following allogeneic hematopoietic stem cell transplantation (allo-HSCT) is critical for efficient pathogen protection and the prevention of graft-versus-host disease (GvHD). In particular, studies...
5.
Esmaeilzadeh H, Jokar-Derisi A, Hassani A, Yazdani R, Delavari S, Abolhassani H, et al.
BMC Immunol
. 2023 Jun;
24(1):9.
PMID: 37312036
Background: Common Variable Immunodeficiency (CVID) is a primary immunodeficiency syndrome resulting in recurrent infections, autoimmunity, and granulomatous manifestations. Methods And Materials: This retrospective study was conducted on an Iranian national...
6.
Sharifinejad N, Azizi G, Rasouli S, Chavoshzadeh Z, Mahdaviani S, Tavakol M, et al.
Biology (Basel)
. 2023 May;
12(5).
PMID: 37237458
Cutaneous manifestations are one of the most common presentations among patients with inborn errors of immunity (IEI). These skin manifestations are often among the first presenting features in the majority...
7.
Bagheri Y, Shad T, Namazi S, Zavareh F, Azizi G, Salami F, et al.
Allergy Asthma Clin Immunol
. 2023 Mar;
19(1):23.
PMID: 36941677
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...
8.
Bayegi S, Hamidieh A, Behfar M, Saghazadeh A, Bozorgmehr M, Karamlou Y, et al.
Transpl Immunol
. 2023 Feb;
77:101803.
PMID: 36842567
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is an effective treatment option for hereditary hemoglobin disorders, such as beta-thalassemia; However, this procedure is not without constraints, mainly engendering complications such as...
9.
Ghadimi S, Jamee M, Abolhassani H, Parvaneh N, Rezaei N, Delavari S, et al.
Allergy Asthma Clin Immunol
. 2023 Feb;
19(1):13.
PMID: 36810129
Background: DCLRE1C gene mutation leads to Artemis deficiency, a severe form of combined immunodeficiency (SCID). Impaired DNA repair and block in early adaptive immunity maturation results in T-B-NK+ immunodeficiency associated...
10.
Azizi G, Fattah Hesari M, Sharifinejad N, Fayyaz F, Chavoshzadeh Z, Mahdaviani S, et al.
J Clin Immunol
. 2023 Feb;
43(4):819-834.
PMID: 36790564
Purpose: Primary B cell defects manifesting as predominantly antibody deficiencies result from variable inborn errors of the B cell lineage and their development, including impairments in early bone marrow development,...