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
1.
Biglari S, Nikuei P, Mir A, Vahidnezhad H, Youssefian L, Moghaddam A, et al.
Clin Genet
. 2024 Dec;
107(3):366-368.
PMID: 39702880
Ataxia with Vitamin E Deficiency (AVED) is a rare autosomal recessive genetic disorder, that caused by pathogenic variants in the TTPA gene, which encodes the alpha-tocopherol transfer protein. This study...
2.
Sadr Z, Ghasemi M, Jafarpour S, Seyfi R, Ghasemi A, Boustanipour E, et al.
Mol Genet Genomics
. 2024 Dec;
300(1):1.
PMID: 39638969
Telomeres, which are situated at the terminal ends of chromosomes, undergo a reduction in length with each cellular division, ultimately reaching a critical threshold that triggers cellular senescence. Cancer cells...
3.
Sadr Z, Ghasemi A, Rohani M, Khorshid H, Habibi-Kavashkohie M, Mohammadi Y, et al.
Neurogenetics
. 2024 Nov;
26(1):12.
PMID: 39607444
Some subtypes of hereditary spastic paraplegia (HSP), especially with autosomal recessive inheritance (AR-HSP), have been reported rarely. In this study, we report the clinical features and molecular results of three...
4.
Esmaeilzadeh E, Biglari S, Mosallaei M, Khorshid H, Vahidnezhad H, Tabatabaiefar M
Mol Genet Genomic Med
. 2024 Nov;
12(11):e70031.
PMID: 39578953
Objective: Mammalian Diaphanous-Related Formin (mDia1), which is encoded by the DIAPH1 gene, serves as essential for the regulation of cell morphology and cytoskeletal organization. The role of DIAPH1 in brain...
5.
Darbandi M, Darbandi M, Darbandi S, Bado I, Hadizadeh M, Khorshid H
Eur J Cancer
. 2024 Jul;
209:114227.
PMID: 39053289
This article delves into the potential of artificial intelligence (AI) to enhance early breast cancer (BC) detection for improved treatment outcomes and patient care. Utilizing a multimethod approach comprising literature...
6.
Maroofi N, Sadat Mousavi Maleki M, Tahmasebi M, Khorshid H, Modaberi Y, Najafipour R, et al.
Mol Biotechnol
. 2024 Apr;
PMID: 38649638
Reactivation of the fetal hemoglobin (HbF) in adult erythroid cells via genome editing is a strategy for the treatment of β-thalassemia and sickle cell disease. In related reports, the reactivation...
7.
Alinaghi S, Mohseni M, Fattahi Z, Beheshtian M, Ghodratpour F, Ashrafi F, et al.
Arch Iran Med
. 2024 Apr;
27(2):79-88.
PMID: 38619031
Background: The study of Y-chromosomal variations provides valuable insights into male susceptibility in certain diseases like cardiovascular disease (CVD). In this study, we analyzed paternal lineage in different Iranian ethnic...
8.
Biglari S, Vahidnezhad H, Tabatabaiefar M, Khorshid H, Esmaeilzadeh E
Mol Genet Genomic Med
. 2024 Apr;
12(4):e2435.
PMID: 38618971
Background: Hypomyelinating leukodystrophy-9 (HLD-9) is caused by biallelic pathogenic variants in RARS1, which codes for the cytoplasmic tRNA synthetase for arginine (ArgRS). This study aims to evaluate the clinical, neuroradiological,...
9.
Feizabadi M, Alerasool M, Eslahi A, Esmaeilzadeh E, Vahidi Mehrjardi M, Saket M, et al.
Biochem Genet
. 2024 Feb;
63(1):22-42.
PMID: 38407766
Bardet-Biedl syndrome (BBS) is a rare inherited ciliopathy disorder characterized by a broad spectrum of clinical symptoms such as retinal dystrophy, obesity, polydactyly, genitourinary and kidney anomalies, learning disability, and...
10.
Zahedipour F, Khorshid H, Esmaeilzadeh E, Kamali K, Ebadifar A
J Dent Res Dent Clin Dent Prospects
. 2023 Nov;
17(3):149-153.
PMID: 38023796
Background: Cleft lip/palate (CL/P) is a prevalent congenital disorder. Matrix metalloproteinases (MMPs) play a role in palatogenesis and have been proposed to be associated with nonsyndromic CL/P development. This study...