Hasil Pencarian - Ali Hosseini Bereshneh

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  1. 1
    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

    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 oleh Ali Hosseini Bereshneh, Masoud Garshasbi

    Diterbitkan 2018-09-01
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  2. 2
    Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report

    Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report oleh Fatemeh Rajabi, Ali Hosseini Bereshneh, Mahboubeh Ramezanzadeh, Masoud Garshasbi

    Diterbitkan 2022-01-01
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  3. 3
    Stem cells: progressions and applications in clinical medicine

    Stem cells: progressions and applications in clinical medicine oleh Ali Hosseini Bereshneh, Danesh Soltani, Reza Roodbarani, Mohammad Hossein Modarressi

    Diterbitkan 2016-05-01
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  4. 4
    Pharmacogenetics and Personalized Medicine in Pancreatic Cancer

    Pharmacogenetics and Personalized Medicine in Pancreatic Cancer oleh Ali Hosseini Bereshneh, Fatemeh Morshedi, Mahsa Hematyar, Arastoo Kaki, Masoud Garshasbi

    Diterbitkan 2017-03-01
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  5. 5
    Horizons of personalized medicine in breast cancer treatment: review article

    Horizons of personalized medicine in breast cancer treatment: review article oleh Ali Hosseini Bereshneh, Danesh Soltani, Negar Veisi, Mohammad Khademi, Mohammad Hossein Modarressi

    Diterbitkan 2016-12-01
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  6. 6
    Frequent Novel Variations Within MSH2 and MLH1 Genes in a Subset of Iranian Families With Hereditary Non-Polyposis Colorectal Cancer

    Frequent Novel Variations Within MSH2 and MLH1 Genes in a Subset of Iranian Families With Hereditary Non-Polyposis Colorectal Cancer oleh Shadi Javan, Alireza Andalib, Ali Hosseini Bereshneh, Mohammad Hassan Emami, Rasul Salehi, Fatemeh Karami

    Diterbitkan 2019-05-01
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  7. 7
    Case Report of RANBP2 Mutation and Familial Acute Necrotizing Encephalopathy

    Case Report of RANBP2 Mutation and Familial Acute Necrotizing Encephalopathy oleh Mohamad Paktinat, Kamran Hessami, Soroor Inaloo, Hamid Nemati, Pegah Katibeh, Marzieh Nejabat, Mohammad Hassan Darabi, Ali Hosseini Bereshneh

    Diterbitkan 2021-01-01
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  8. 8
    Methylation Assessment of Two DKK2 and DKK4 Genes in Oral Squamous Cell Carcinoma Patients

    Methylation Assessment of Two DKK2 and DKK4 Genes in Oral Squamous Cell Carcinoma Patients oleh Sedigheh KHEIRANDISH, Nosratollah ESHGHYAR, Farzad YAZDANI, Pouyan AMINI SHAKIB, Ali HOSSEINI-BERESHNEH, Zahra NOURI, Ali KHEIRANDISH, Fatemeh KARAMI

    Diterbitkan 2020-10-01
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  9. 9
    Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy

    Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy oleh Gholamreza Zamani, Sareh Hosseinpour, Mahmoud Reza Ashrafi, Mahmoud Mohammadi, Reza Shervin Badv, Ali Reza Tavasoli, Masood Ghahvechi Akbari, Ali Hosseini Bereshneh, Reza Azizi Malamiri, Morteza Heidari

    Diterbitkan 2022-05-01
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