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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Articles
102
Citations
1460
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Recent Articles
11.
Esmaeilzadeh E, Jafari Harandi A, Astaraki F, Khorshid H
Psychiatr Genet
. 2023 Nov;
34(1):8-14.
PMID: 38019139
White-Sutton Syndrome is one of the rare neurodevelopmental disorder inherited in an autosomal dominant manner, mainly caused by de novo mutations in the POGZ gene and shows many phenotypic signs...
12.
Ashrafi F, Mohseni M, Beheshtian M, Fattahi Z, Ghodratpour F, Keshavarzi F, et al.
Arch Iran Med
. 2023 Aug;
26(2):69-75.
PMID: 37543926
Background: Global real-time monitoring of SARS-CoV-2 variants is crucial to controlling the COVID-19 outbreak. The purpose of this study was to set up a Sanger-based platform for massive SARS-CoV-2 variant...
13.
Fattahi Z, Mohseni M, Beheshtian M, Jafarpour A, Jalalvand K, Keshavarzi F, et al.
Arch Iran Med
. 2023 Aug;
25(8):508-522.
PMID: 37543873
Background: Complete SARS-CoV-2 genome sequencing in the early phase of the outbreak in Iran showed two independent viral entries. Subsequently, as part of a genome surveillance project, we aimed to...
14.
Esmaeilzadeh E, Moradi A, Khorshid H
CEN Case Rep
. 2023 Mar;
12(4):374-377.
PMID: 36856752
Galloway-Mowat syndrome is a rare autosomal-recessive genetic disorder that is characterized by variety of complications such as neurological abnormalities and early-onset progressive kidney disease. Studies have been shown that pathogenic...
15.
Zeinaloo A, Ilali H, Moghadam E, Khorshid H, Esmaeilzadeh E
Iran J Public Health
. 2023 Feb;
51(12):2826-2830.
PMID: 36742244
Mulibrey Nanism is a rare multisystem disorder inherited in an autosomal recessive manner caused by mutations in the gene. Most of the reported cases are from Finland, but this condition...
16.
Saliminejad K, Mahmoodzadeh H, Soleymani Fard S, Yaghmaie M, Khorshid H, Mousavi S, et al.
Avicenna J Med Biotechnol
. 2022 Dec;
14(4):278-286.
PMID: 36504565
Background: The high mortality rate of Gastric Cancer (GC) is a consequence of delayed diagnosis. The early diagnosis of GC could increase the five-year survival rate among patients. We aimed...
17.
Esmaeilzadeh E, Soleimani M, Khorshid H
Mult Scler Relat Disord
. 2022 Aug;
67:104076.
PMID: 35961059
Multiple sclerosis (MS) is a multifactorial chronic inflammatory demyelinating disease of the central nervous system with both immune and neurodegenerative components as the underlying causes. Cytokines are key components of...
18.
Soleymani M, Ebadifar A, Khosravi M, Esmaeilzadeh E, Khorshid H
Avicenna J Med Biotechnol
. 2022 May;
14(2):181-185.
PMID: 35633982
Background: Non-syndromic cleft lip occurs by the interaction of environmental and genetic factors. The purpose of the current study was to analyze the association of Single Nucleotide Polymorphisms (SNPs) in...
19.
Esmaeilzadeh E, Ghaderi Z, Moradi A, Khorshid H
CEN Case Rep
. 2022 Feb;
11(4):404-407.
PMID: 35179696
Pathogenic variants in FAT1 gene have recently been described in association with coloboma, nephropathy, and facial dismorphism. Here we describe a 5-year-old Iranian boy with iris coloboma and nephropathy, born...
20.
Darbandi S, Darbandi M, Khorshid H, Sengupta P
World J Mens Health
. 2022 Jan;
40(3):442-455.
PMID: 35021309
Purpose: Oocytes and spermatozoa are electrogenic cells with the ability to respond to electrical stimuli and modulate their electrical properties accordingly. Determination of the ionic events during the gamete maturation...