Hasil Pencarian - Isa Abdi Rad

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  1. 1
    Report of a Novel Splicing Mutation in the Gene in a Patient With Sensorineural Hearing Loss and Spectrum of the Mutations

    Report of a Novel Splicing Mutation in the Gene in a Patient With Sensorineural Hearing Loss and Spectrum of the Mutations oleh Elinaz Akbariazar, Ali Vahabi, Isa Abdi Rad

    Diterbitkan 2019-09-01
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  2. 2
    A novel GTPBP2 splicing mutation in two siblings affected with microcephaly, generalized muscular atrophy, and hypotrichosis

    A novel GTPBP2 splicing mutation in two siblings affected with microcephaly, generalized muscular atrophy, and hypotrichosis oleh Isa Abdi Rad, Ali Vahabi, Elinaz Akbariazar

    Diterbitkan 2021-02-01
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  3. 3
    The use of stromal vascular fraction (SVF), platelet-rich plasma (PRP) and stem cells in the treatment of osteoarthritis: an overview of clinical trials

    The use of stromal vascular fraction (SVF), platelet-rich plasma (PRP) and stem cells in the treatment of osteoarthritis: an overview of clinical trials oleh Sahar Mehranfar, Isa Abdi Rad, Ebrahim Mostafavi, Abolfazl Akbarzadeh

    Diterbitkan 2019-12-01
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  4. 4
    Vitamin D Receptor TaqI Gene Variant in Exon 9 and Polycystic Ovary Syndrome Risk

    Vitamin D Receptor TaqI Gene Variant in Exon 9 and Polycystic Ovary Syndrome Risk oleh Morteza Bagheri, Isa Abdi Rad, Nima Hosseini Jazani, Fariba Nanbakhsh

    Diterbitkan 2013-07-01
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  5. 5
    C677T and A1298C Mutations in the Methylenetetrahydrofolate Reductase Gene in Patients with Recurrent Abortion from the Iranian Azeri Turkish

    C677T and A1298C Mutations in the Methylenetetrahydrofolate Reductase Gene in Patients with Recurrent Abortion from the Iranian Azeri Turkish oleh Morteza Bagheri, Isa Abdi Rad, Mir Davood Omrani, Fariba Nanbakhsh

    Diterbitkan 2010-10-01
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  6. 6
    جهش اکتسابی تیروزین کیناز JAK2 V617F در بيماری‌های Myeloproliferative مزمن ABL-BCR منفی در یک جمعیت از استان آذربایجان غربی

    جهش اکتسابی تیروزین کیناز JAK2 V617F در بيماری‌های Myeloproliferative مزمن ABL-BCR منفی در یک جمعیت از استان آذربایجان غربی... oleh Morteza Bagheri, Isa Abdi-Rad, Davood Malek, Ali Eishi, Nasim Valizadeh

    Diterbitkan 2018-02-01
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  7. 7
    Mutation analysis of the phenylalanine hydroxylase gene in Azerbaijani population, a report from West Azerbaijan province of Iran

    Mutation analysis of the phenylalanine hydroxylase gene in Azerbaijani population, a report from West Azerbaijan province of Iran oleh Morteza Bagheri, Isa Abdi Rad, Nima Hosseini Jazani, Rasoul Zarrin, Ahad Ghazavi

    Diterbitkan 2015-07-01
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  8. 8
    Zinc Protects against MDMA-Induced Apoptosis of Sertoli Cells in Mouse via Attenuation of Caspase-3

    Zinc Protects against MDMA-Induced Apoptosis of Sertoli Cells in Mouse via Attenuation of Caspase-3 oleh Nadia Hossein-Zadeh, Morteza Bagheri, Isa Abdi Rad, Marziyeh Lozeie, Mahdieh Nasir-Zadeh

    Diterbitkan 2020-10-01
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  9. 9
    Zinc attenuates ecstasy-induced apoptosis through downregulation of caspase-3 in cultured TM3 cells: An experimental study

    Zinc attenuates ecstasy-induced apoptosis through downregulation of caspase-3 in cultured TM3 cells: An experimental study oleh Marziyeh Lozeie, Morteza Bagheri, Isa Abdi Rad, Nadia Hossein-Zadeh, Mahdyieh Nasir-Zadeh

    Diterbitkan 2020-09-01
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  10. 10
    A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy

    A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy oleh Saeed Farajzadeh Valilou, Javad Karimzad Hagh, Mohammad Salimi Asl, Isa Abdi Rad, Masoud Edizadeh, Arash Pooladi

    Diterbitkan 2021-08-01
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  11. 11
    Frequency of the R202Q mutation of MEFV gene in Iranian patients with premature coronary artery disease: a report from West Azerbaijan province of Iran

    Frequency of the R202Q mutation of MEFV gene in Iranian patients with premature coronary artery disease: a report from West Azerbaijan province of Iran oleh Morteza Bagheri, Kamal Khadem-Vatani, Isa Abdi Rad, MirHossein Seyed-Mohammadzad, Alireza Rostamzadeh, Behzad Rahimi, Negin Kavosi

    Diterbitkan 2024-04-01
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  12. 12
    Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran

    Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran oleh Morteza Bagheri, Kamal Khadem-Vatani, Mir Hossein Seyed Mohammad Zad, Isa Abdi Rad, Behzad Rahimi, Alireza Rostamzadeh, Mojtaba Godarzi, Shabnam Ashena

    Diterbitkan 2018-03-01
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