Reza Boostani
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Explore the profile of Reza Boostani including associated specialties, affiliations and a list of published articles.
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99
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579
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Recent Articles
1.
Rad P, Vahidi Z, Zemorshidi M, Farzadfard M, Khadem-Rezaiyan M, Boostani R, et al.
Cytokine
. 2024 Dec;
185:156825.
PMID: 39631261
Human T-lymphotropic virus type 1 (HTLV-1), leads to adult T-cell lymphoma/leukemia (ATL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) in a minority of infected individuals. The virus promotes inflammation, a major...
2.
Taheri N, Fani M, Khanbabaei H, Vahidi Z, Zemorshidi F, Boostani R, et al.
Viral Immunol
. 2024 Nov;
37(9):446-450.
PMID: 39504971
Human T-cell lymphotropic virus type-I (HTLV-I)-associated myelopathy/tropical spastic paraparesis (HAM/TSP), the main neurological manifestation of HTLV-I, is a chronic inflammatory disease. Viral-host interaction and host genetics are two important contributors...
3.
Lankarani K, Aboulpor N, Boostani R, Saeian S
Neurogastroenterol Motil
. 2024 Oct;
36(12):e14931.
PMID: 39370611
Background: Esophageal motility disorders are mainly evaluated with high-resolution manometry (HRM) which is a time-consuming and uncomfortable procedure with potential adverse events. Acoustic characterization of the swallowing has the potential...
4.
Calame D, Wong J, Panda P, Nguyen D, Leong N, Sangermano R, et al.
Genet Med
. 2024 Sep;
27(1):101273.
PMID: 39306721
Purpose: FLVCR1 encodes a solute carrier protein implicated in heme, choline, and ethanolamine transport. Although Flvcr1 mice exhibit skeletal malformations and defective erythropoiesis reminiscent of Diamond-Blackfan anemia (DBA), biallelic FLVCR1...
5.
Sabeghi D, InanlooRahatloo K, Mirzadeh H, Khani M, Shamshiri H, Taghavi T, et al.
Acta Neurol Belg
. 2024 Jul;
124(4):1363-1370.
PMID: 38965176
Introduction: Riboflavin Transporter Deficiency (RTD) is a rare neurological disorder characterized by pontobulbar palsy, hearing loss, and motor cranial nerve involvement. SLC52A3 and SLC52A2 mutations are causes of RTD. SLC52A2...
6.
Najarzadeh Torbati P, Doosti M, Sarraf P, Boostani R, Ahangari N, Toosi M, et al.
Iran J Public Health
. 2024 Jun;
53(5):1184-1191.
PMID: 38912134
Background: Plectinopathy-associated disorders are caused by mutations in the gene encoding Plectin protein. mutations cause a spectrum of diseases defined by varying degrees of signs, mostly with epidermolysis bullosa simplex...
7.
Ziaadini B, Ghaderi Yazdi B, Dirandeh E, Boostani R, Karimi N, Panahi A, et al.
BMC Neurol
. 2024 Jun;
24(1):211.
PMID: 38907197
Background: Congenital myasthenic syndromes (CMS) are among the most challenging differential diagnoses in the neuromuscular domain, consisting of diverse genotypes and phenotypes. A mutation in the Docking Protein 7 (Dok-7)...
8.
Davoudi M, Boostani R, Manzari Z
Iran J Med Sci
. 2024 May;
49(5):294-301.
PMID: 38751877
Background: Human T-cell Leukemia Virus type-1 (HTLV-1) -associated myelopathy causes sufferers to experience changes in several aspects of their lives. Gaining a deeper understanding of these changes can help healthcare...
9.
Fadaee A, Mohammadi F, Ariaee N, Ahmadi Ghezeldasht S, Valizadeh N, Kheradmand F, et al.
Mult Scler Relat Disord
. 2024 May;
87:105659.
PMID: 38704874
Background/aim: The roles of endocannabinoids are described in immune modulation and neuroprotection. HTLV-1-associated myelopathy (HAM/TSP) is an inflammatory neurodegenerative disease. Therefore, in this study, the interactions of HTLV-1 regulatory factors...
10.
Ariaee N, Abbasnia S, Sabet F, Mirhossein A, Ahmadi Ghezeldasht S, Moshfegh M, et al.
Rep Biochem Mol Biol
. 2024 Apr;
12(3):393-402.
PMID: 38618262
Background: The significance of HTLV-1 proviral load as a prognostic biomarker in HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) has been a subject of controversy. This study aims to assess the impact...