Mohammad Miryounesi
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Explore the profile of Mohammad Miryounesi including associated specialties, affiliations and a list of published articles.
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64
Citations
220
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Recent Articles
1.
Aghaei-Zarch S, Mahmoudieh L, Miryounesi M, Aghazadeh M, Reihani-Ardabili M, Zamani M, et al.
Cytokine
. 2025 Feb;
188:156892.
PMID: 39970816
Background: Diabetic nephropathy (DN) is a significant driver of end-stage renal disease, requiring kidney replacement therapies such as transplantation and dialysis. Given the critical importance of understanding the onset and...
2.
Ghasemi M, Esmaeilizadeh Z, Tehrani Fateh S, Sadeghi H, Bagheri S, Hashemi-Gorji F, et al.
Mol Genet Genomic Med
. 2025 Jan;
13(1):e70057.
PMID: 39835750
Background: X-linked intellectual disability (XLID) is a genetically heterogeneous disorder that results in cognitive impairment and developmental delays. Mutations in the KDM5C gene have been identified as a causative factor...
3.
Fathi M, Khalilian S, Miryounesi M, Ghafouri-Fard S
Biochem Genet
. 2025 Jan;
PMID: 39806039
Metachromatic leukodystrophy (MLD) is an autosomal recessive disorder caused by mutations in the arylsulfatase A (ARSA) gene. Few studies have assessed the spectrum of ARSA mutations among Iranian patients. Here,...
4.
Ghasemi M, Tehrani Fateh S, Ben-Mahmoud A, Gupta V, Stuhn L, Lesca G, et al.
Am J Med Genet A
. 2024 Dec;
:e63963.
PMID: 39707601
The Houge type of X-linked syndromic intellectual developmental disorder (MRXSHG) encompasses a spectrum of neurodevelopmental disorders characterized by intellectual disability (ID), language/speech delay, attention issues, and epilepsy. These conditions arise...
5.
Khalilian S, Fathi M, Ghahghaei-Nezamabadi A, Miryounesi M, Ghafouri-Fard S
Neurogenetics
. 2024 Dec;
26(1):14.
PMID: 39627470
Neurodegeneration with brain iron accumulation 5 (NBIA5) is a distinctive type of NBIA phenotype that is caused by mutations in the WDR45 gene. This disorder is inherited in an X-linked...
6.
Moeinafshar A, Tehrani Fateh S, Hashemi-Gorji F, Karimzadeh P, Gholibeglou E, Rostami M, et al.
BMC Neurol
. 2024 Nov;
24(1):455.
PMID: 39567938
Background: Hereditary sensory and autonomic neuropathy type 9 (HSAN9) is a rare genetic disorder caused by genetic alterations in the TECPR2 locus and is characterized by developmental and intellectual disability,...
7.
Alijanpour S, Ghafouri-Fard S, Tonekaboni S, Karimzadeh P, Ahmadabadi F, Rahimian E, et al.
Basic Clin Neurosci
. 2024 Nov;
15(4):541-552.
PMID: 39553263
Introduction: Developmental and epileptic encephalopathy 9 (DEE9) is caused by pathogenic variants in the gene. The clinical features include early-onset seizures that are often provoked by fever and display clustered...
8.
Altered expression of Csnk1a1p in Autism Spectrum Disorder in Iranian population: case-control study
Rahmani Z, Rahmani D, Jazi M, Ghasemi M, Sadeghi H, Miryounesi M, et al.
Sci Rep
. 2024 Nov;
14(1):28307.
PMID: 39550379
Over the past decade, substantial scientific evidence has showed that long non-coding RNAs (lncRNAs) are extensively expressed and play a crucial role in gene modulation through a diverse range of...
9.
Khalilian S, Fathi M, Miryounesi M, Ghafouri-Fard S
Neurol Sci
. 2024 Oct;
46(2):999-1007.
PMID: 39470906
Aicardi-Goutières syndrome (AGS) is a rare neurodevelopmental disorder that can be misdiagnosed with infectious disorders. Molecular genetics tools and subsequent counseling have an important role in the estimation of recurrence...
10.
Cali E, Quirin T, Rocca C, Efthymiou S, Riva A, Marafi D, et al.
Genet Med
. 2024 Sep;
:101251.
PMID: 39275948
Purpose: This study aims to comprehensively delineate the phenotypic spectrum of ACTL6B-related disorders, previously associated with both autosomal recessive and autosomal dominant neurodevelopmental disorders. Molecularly, the role of the nucleolar...