Hasil Pencarian - Masoumeh Falah

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  1. 1
    پیرگوشی: از دانش کنونی تا چشم‌اندازهای آینده‌ی درمان

    پیرگوشی: از دانش کنونی تا چشم‌اندازهای آینده‌ی درمان oleh Masoumeh Falah, Massoud Houshmand, Mohammad Farhadi

    Diterbitkan 2016-07-01
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  2. 2
    پیش‌بینی بهزیستی روان‌شناختی بر اساس مؤلفه‌های نگرش مذهبی و حرمت خود در سالمندان شهر اهواز

    پیش‌بینی بهزیستی روان‌شناختی بر اساس مؤلفه‌های نگرش مذهبی و حرمت خود در سالمندان شهر اهواز oleh Nahid Karimi, Sara Mousavi, Masoumeh Falah-Neudehi

    Diterbitkan 2020-12-01
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  3. 3
    Emotion Regulation Training on Irritability, Alexithymia, and Interpersonal Problems of Adolescents With Disruptive Mood Dysregulation Disorder

    Emotion Regulation Training on Irritability, Alexithymia, and Interpersonal Problems of Adolescents With Disruptive Mood Dysregulation Disorder oleh Masoumeh Falah Neudehi, Farnaz Rezaei, Ameneh Bozorgi Kazerooni, Zahra Ebadi

    Diterbitkan 2023-10-01
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  4. 4
    Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness

    Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness oleh Sima Rayat, Mohammad Farhadi, Hessamaldin Emamdjomeh, Saeid Morovvati, Masoumeh Falah

    Diterbitkan 2022-06-01
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  5. 5
    Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation

    Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation oleh Masoumeh Falah, Massoud Houshmand, Susan Akbaroghli, Saeid Mahmodian, Yaser Ghavami, Mohammad Farhadi

    Diterbitkan 2011-05-01
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  6. 6
    The genetic landscape and possible therapeutics of neurofibromatosis type 2

    The genetic landscape and possible therapeutics of neurofibromatosis type 2 oleh Mohammad Amin Ghalavand, Alimohamad Asghari, Mohammad Farhadi, Farzad Taghizadeh-Hesary, Masoud Garshasbi, Masoumeh Falah

    Diterbitkan 2023-05-01
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  7. 7
    Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population

    Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population oleh Sima Rayat, Nasim Ramezanidoraki, Nima Kazemi, Mohammad H. Modarressi, Masoumeh Falah, Safoura Zardadi, Saeid Morovvati

    Diterbitkan 2022-06-01
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  8. 8
    Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12

    Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12 oleh Ahmad Daneshi, Masoud Garshasbi, Mohammad Farhadi, Khalil Ghasemi Falavarjani, Mohammad Vafaee-Shahi, Navid Almadani, MohammadSina Zabihi, Mohammad Amin Ghalavand, Masoumeh Falah

    Diterbitkan 2023-10-01
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