Hasil Pencarian - Akram Sarmadi

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  1. 1
    Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia

    Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsi... oleh Zahra Nouri, Akram Sarmadi, Sina Narrei, Hamidreza Kianersi, Farzan Kianersi, Mohammad Amin Tabatabaiefar

    Diterbitkan 2024-07-01
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  2. 2
    Molecular genetic study in a cohort of Iranian families suspected to maturity-onset diabetes of the young, reveals a recurrent mutation and a high-risk variant in the CEL gene

    Molecular genetic study in a cohort of Iranian families suspected to maturity-onset diabetes of the young, reveals a recurrent mutation and a high-risk variant in the CEL gene oleh Akram Sarmadi, Aliasgar Mohammadi, Fatemeh Tabatabaei, Zahra Nouri, Morteza Hashemzadeh Chaleshtori, Mohammad Amin Tabatabaiefar

    Diterbitkan 2020-01-01
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  3. 3
    Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran

    Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran oleh Aliasgar Mohammadi, Ameneh Eskandari, Akram Sarmadi, Mehrali Rahimi, Bijan Iraj, Mahin Hashemipour, Morteza Hashmezadeh Chaleshtori, Mohammad Amin Tabatabaiefar

    Diterbitkan 2019-01-01
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  4. 4
    Alteration in CD8+ T cell subsets in enterovirus-infected patients: An alarming factor for type 1 diabetes mellitus

    Alteration in CD8+ T cell subsets in enterovirus-infected patients: An alarming factor for type 1 diabetes mellitus oleh Omid Zargari Samani, Lila Mahmoodnia, Maryam Izad, Hedayatollah Shirzad, Azam Jamshidian, Mahdi Ghatrehsamani, Soleiman Kheiri, Ladan Sadeghian, Amin Soltani, Akram Sarmadi

    Diterbitkan 2018-05-01
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  5. 5
    A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family

    A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family oleh Akram Sarmadi, Samane Nasrniya, Maryam Soleimani Farsani, Sina Narrei, Zahra Nouri, Mahsa Sepehrnejad, Mohammad Hussein Nilforoush, Hamidreza Abtahi, Mohammad Amin Tabatabaiefar

    Diterbitkan 2020-06-01
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