Hamid Reza Khorram Khorshid
Overview
Explore the profile of Hamid Reza Khorram Khorshid including associated specialties, affiliations and a list of published articles.
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102
Citations
1460
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Recent Articles
21.
Ghaffari S, Rafati M, Shadnoush M, Pourbabaee S, Aghighi M, Mirab Samiee S, et al.
Hum Mutat
. 2022 Jan;
43(4):e1-e23.
PMID: 35005816
Mucopolysaccharidoses (MPSs) are rare, heterogeneous inborn errors of metabolism (IEM) diagnosed through a combination of clinical, biochemical, and genetic investigations. The aim of this study was molecular characterization of the...
22.
Dehani M, Zare-Abdollahi D, Bushehri A, Dehghani A, Effati J, Miratashi S, et al.
Avicenna J Med Biotechnol
. 2021 Dec;
13(4):230-233.
PMID: 34900151
Background: Bardet-Biedl Syndrome (BBS) is a rare pleiotropic autosomal recessive disease related to ciliopathies with approximately 25 causative genes. BBS is a multisystemic disorder with wide spectrum of manifestations including...
23.
Hassani M, Soleimani M, Esmaeilzadeh E, Zare-Abdollahi D, Khorshid H
Iran J Pharm Res
. 2021 Apr;
19(4):321-329.
PMID: 33841545
The present study was designed to primarily examine the therapeutic potential of the herbal extract of for the treatment of multiple sclerosis in the experimental autoimmune encephalomyelitis (EAE) model of...
24.
Nasrollahzadeh Sabet M, Biglari S, Khorshid H, Esmaeilzadeh E
J Pharm Pharmacol
. 2020 Sep;
72(12):1970-1976.
PMID: 32892382
Objectives: Multiple sclerosis is a common autoimmune inflammatory disease of the central nervous system. There are several underlying mechanisms for the pathogenesis of the disease, including inflammation, oligodendrocyte apoptosis and...
25.
Darbandi S, Darbandi M, Agarwal A, Khorshid H, Sadeghi M, Esteves S, et al.
Int J Reprod Biomed
. 2020 Aug;
18(6):425-438.
PMID: 32754678
Background: The three-parent assisted reproductive technique may increase oocyte competence. Objective: In this case-control study, the suitability of germinal vesicle transfer (GVT), synchronous ooplasmic transfer (sOT), asynchronous ooplasmic transfer using...
26.
Bushehri A, Zare-Abdollahi D, Alavi A, Dehghani A, Mousavimikala M, Khorshid H
Int J Mol Cell Med
. 2020 Jun;
8(3):179-190.
PMID: 32489947
Homozygous mutations of PROS1, encoding vitamin K-dependent protein S (PS), have been reported so far to be associated with purpura fulminans, a characteristic fatal venous thromboembolic disorder. The current work...
27.
Saliminejad K, Soleymani Fard S, Khorshid H, Yaghmaie M, Mahmoodzadeh H, Mousavi S, et al.
Avicenna J Med Biotechnol
. 2020 May;
12(2):99-106.
PMID: 32431794
Background: Most of Gastric Cancer (GC) patients are diagnosed at an advanced stage with poor prognosis. Hypermethylations of several tumor suppressor genes in cell-free DNA of GC patients have been...
28.
Bushehri A, Zare-Abdollahi D, Hashemian H, Safavizadeh L, Effati J, Khorshid H
Iran Biomed J
. 2020 Apr;
24(4):257-63.
PMID: 32306724
Background: The clinical phenotyping of patients with achromatopsia harboring variants in phosphordiesterase 6C (PDE6C) has poorly been described in the literature. PDE6C encodes the catalytic subunit of the cone phosphodiesterase,...
29.
Heidary Z, Zaki-Dizaji M, Saliminejad K, Edalatkhah H, Khorshid H
Andrologia
. 2020 Feb;
52(3):e13539.
PMID: 32030798
Asthenozoospermia (AZS), which characterised by reduced forward sperm motility, is a common cause of male infertility. Recently, mitochondrial dysfunction reported in AZS men came to attention for finding the molecular...
30.
Safari S, Zare-Abdollahi D, Bushehri A, Safari M, Dehghani A, Tahmasebi Z, et al.
J Gene Med
. 2020 Jan;
22(3):e3154.
PMID: 31957135
Bachground: Leber congenital amaurosis (LCA) is a severe and congenital or early onset form of inherited retinitis pigmentosa (RP). To date, approximately 25 genes have been introduced in relation to...