Shahram Torkamandi
Overview
Explore the profile of Shahram Torkamandi including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
160
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Recent Articles
1.
Babaie F, Omraninava M, Mahdavi Gorabi A, Khosrojerdi A, Aslani S, Yazdchi A, et al.
Curr Genomics
. 2023 Feb;
23(3):163-174.
PMID: 36777004
Psoriasis is an organ-specific autoimmune disease characterized by the aberrant proliferation and differentiation of keratinocytes, leading to skin lesions. Abnormal immune responses mediated by T cells and dendritic cells and...
2.
Torkamandi S, Bahrami S, Ghorashi T, Dehani M, Bayat H, Hoseini S, et al.
Genes Immun
. 2021 Nov;
22(7-8):322-326.
PMID: 34782775
Long noncoding RNA MEG3 and NLRC5 genes are both involved in the immune system and the regulation of NLRC5 by MEG3 is documented in rheumatoid arthritis. Therefore, we intended to...
3.
Aghdam A, Rezaei S, Zarza Nalivan F, Babaie F, Amiri Nikpour M, Torkamandi S
Immunol Invest
. 2021 Apr;
51(5):1149-1161.
PMID: 33866949
Multiple sclerosis (MS) is a chronic neuroinflammatory disease of the brain and spinal cord. Evidences have demonstrated that microRNAs (miRNAs) are involved in the pathological process of MS that may...
4.
Ebrazeh M, Ezzatifar F, Torkamandi S, Mohammadi F, Salimifard S, Shabgah A, et al.
Int J Rheum Dis
. 2021 Feb;
24(4):567-581.
PMID: 33550689
Background: Genetic polymorphisms in the endoplasmic reticulum aminopeptidase gene ERAP2 has been attributed with the etiopathogenesis of ankylosing spondylitis (AS). Here we assessed the association of ERAP2 gene single nucleotide...
5.
Amini M, Shomali N, Bakhshi A, Rezaei S, Hemmatzadeh M, Hosseinzadeh R, et al.
Int Immunopharmacol
. 2020 Nov;
88:107024.
PMID: 33182024
The human gastrointestinal microbiota, also known as the gut microbiota living in the human gastrointestinal tract, has been shown to have a significant impact on several human disorders including rheumatoid...
6.
Ghaderian S, Shomali N, Behravesh S, Danbaran G, Hemmatzadeh M, Aslani S, et al.
J Neuroimmunol
. 2020 Aug;
347:577347.
PMID: 32745803
Multiple sclerosis (MS) is the most common inflammatory demyelinating disease of the central nervous system (CNS) with various clinical manifestations. The characteristic of MS is that myelin is attacked by...
7.
Mohammadhosayni M, Khosrojerdi A, Lorian K, Aslani S, Imani D, Razi B, et al.
BMC Neurol
. 2020 May;
20(1):218.
PMID: 32471473
Background: Several studies have reported the association between polymorphisms in Matrix metalloproteinases (MMPs) gene family and risk of Multiple sclerosis (MS). However, the results have been inconsistent and inconclusive. To...
8.
Torkamandi S, Rezaei S, Mirfakhraie R, Bayat S, Piltan S, Gholami M
J Clin Lab Anal
. 2020 May;
34(8):e23358.
PMID: 32419160
Background: Wolfram's syndrome (WFS) is a hereditary (autosomal recessive) neurodegenerative disorder. The clinical features are related to diabetes insipidus, diabetes mellitus, optic atrophy, and deafness (DIDMOAD) with other variable clinical...
9.
Torkamandi S, Rezaei S, Mirfakhraie R, Golmohamadi S, Gholami M
Mol Biol Rep
. 2020 Apr;
47(5):4021-4027.
PMID: 32281057
Background: Biotinidase deficiency is an autosomal recessive inherited inborn error of biotin metabolism. Biotin as a water-soluble vitamin is the prosthetic group of biotin-dependent carboxylase enzymes, and by enhancing their...
10.
Omidvar M, Torkamandi S, Rezaei S, Alipoor B, Omrani M, Darvish H, et al.
J Neurol
. 2019 Nov;
268(6):2065-2082.
PMID: 31745725
Aims: The hereditary spastic paraplegias (HSPs) are a heterogeneous group of inherited neurodegenerative disorders. Although, several genotype-phenotype studies have carried out on HSPs, the association between genotypes and clinical phenotypes...