- Gholamreza Z, Hosseinpour S, Ashrafi MR, Mohammadi M, Badv RS, Tavasoli AR, Akbari MG, Hosseini Bereshneh A, Malamiri RA, Heidari M (2022) Characteristics of Disease Progression and Genetic Correlation in Ambulatory Iranian Boys with Duchenne Muscular Dystrophy. BMC Neurology 22(1):162. [Abstract]
- Fatemeh R*, Hosseini Bereshneh A*, Ramezanzadeh M, Garshasbi M (2022) Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report. BMC Pediatrics 22(1):1-6. *contributed equally [Abstract]
- Hosseini Bereshneh A, Jafarinia E, Rajabi F, Ashrafi MR, Tavasoli AR, Garshasbi M (2021) Crystallographic modeling of the PNPT1: c. 1453A> G variant as a cause of mitochondrial dysfunction and autosomal recessive deafness; expanding the neuroimaging and clinical features. Mitochondrion 59:1-7. [Abstract]
- Mohamad P, Hessami K, Inaloo S, Nemati H, Katibeh P, Nejabat M, Darabi MH, Hosseini Bereshneh A (2021) Case report of RANBP2 mutation and familial acute necrotizing encephalopathy. International Journal of Pediatrics :doi: 10.1155/2021/6695119. [Abstract]
- Masoudi M, Hosseini Bereshneh A, Rasoulinezhad M, Ashrafi MR, Garshasbi M, Tavasoli AR (2020) Leukoencephalopathy in Al-Raqad Syndrome: Expanding the clinical and neuroimaging features caused by a biallelic novel missense variant in DCPS. American journal of medical genetics 182(10):2391-2398. [Abstract]
- Gholamreza Z, Hosseini Bereshneh A, Malamiri RA, Bagheri S, Moradi K, Ashrafi MR, Tavasoli AR, Mohammadi M, Badv RS, Akbari MG, Heidari M (2020) The first comprehensive cohort of the Duchenne muscular dystrophy in Iranian population: mutation spectrum of 314 patients and identifying two novel nonsense mutations. Journal of Molecular Neuroscience 70(10):1565-1573. [Abstract]
- Hosseini Bereshneh A, Hosseipour S, Rasoulinezhad MS, Pak N, Garshasbi M, Tavasoli AR (2020) Expanding the clinical and neuroimaging features of NKX6-2-related hereditary spastic ataxia type 8. European Journal of Medical Genetics 63(5):103868. [Abstract]
- Hosseini Bereshneh A, Garshasbi M (2018) Novel in-frame deletion in MFSD8 gene revealed by trio whole exome sequencing in an Iranian affected with neuronal ceroid lipofuscinosis type 7: a case report. Journal of Medical Case Reports 12(1):281. [Abstract]
- Salmaninejad A, Zamani MR, Pourvahedi M, Golchehre Z, Hosseini Bereshneh A, Rezaei N (2016) Cancer/testis antigens: expression, regulation, tumor invasion, and use in immunotherapy of cancers. Immunological investigations 45(7):619-640. [Abstract]
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