Ali Hosseini Bereshneh to Humans
This is a "connection" page, showing publications Ali Hosseini Bereshneh has written about Humans.
Connection Strength
0.058
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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. 2021 07; 59:1-7.
Score: 0.015
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Expanding the clinical and neuroimaging features of NKX6-2-related hereditary spastic ataxia type 8. Eur J Med Genet. 2020 May; 63(5):103868.
Score: 0.014
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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. J Med Case Rep. 2018 Sep 25; 12(1):281.
Score: 0.012
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Pharmacogenetics and Personalized Medicine in Pancreatic Cancer. Acta Med Iran. 2017 Mar; 55(3):194-199.
Score: 0.011
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The First Comprehensive Cohort of the Duchenne Muscular Dystrophy in Iranian Population: Mutation Spectrum of 314 Patients and Identifying Two Novel Nonsense Mutations. J Mol Neurosci. 2020 Oct; 70(10):1565-1573.
Score: 0.003
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Cancer/Testis Antigens: Expression, Regulation, Tumor Invasion, and Use in Immunotherapy of Cancers. Immunol Invest. 2016 Oct; 45(7):619-40.
Score: 0.003