Hasil Pencarian - Sahand Tehrani Fateh

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  1. 1
    Novel BRAT1 variant associated with neurodevelopmental disorder with cerebellar atrophy and seizure: Case report and a literature review

    Novel BRAT1 variant associated with neurodevelopmental disorder with cerebellar atrophy and seizure: Case report and a literature review oleh Mohammad-Reza Ghasemi, Sahand Tehrani Fateh, Farzad Hashemi-Gorji, Morteza Sheikhi Nooshabadi, Sahar Alijanpour, Ali Mardi, Mohammad Miryounesi

    Diterbitkan 2024-01-01
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  2. 2
    Expanding genetic and clinical aspects of Schwartz-Jampel syndrome: A report of two cases with literature review

    Expanding genetic and clinical aspects of Schwartz-Jampel syndrome: A report of two cases with literature review oleh Iman Elahi Vahed, Sahand Tehrani Fateh, Melika Kamali, Farzad Hashemi-Gorji, Zahra Esmaeilzadeh, Hossein Sadeghi, Mohammad Miryounesi, Mohammad-Reza Ghasemi

    Diterbitkan 2024-09-01
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  3. 3
    Non-coding RNAs as potential therapeutic targets for receptor tyrosine kinase signaling in solid tumors: current status and future directions

    Non-coding RNAs as potential therapeutic targets for receptor tyrosine kinase signaling in solid tumors: current status and future directions oleh Aysan Moeinafshar, Mohammad Nouri, Nima Shokrollahi, Mahdi Masrour, Amirmohammad Behnam, Sahand Tehrani Fateh, Hossein Sadeghi, Mohammad Miryounesi, Mohammad-Reza Ghasemi

    Diterbitkan 2024-01-01
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  4. 4
    The Effects of Sesquiterpene Lactones on the Differentiation of Human or Animal Cells Cultured In-Vitro: A Critical Systematic Review

    The Effects of Sesquiterpene Lactones on the Differentiation of Human or Animal Cells Cultured In-Vitro: A Critical Systematic Review oleh Sepand Tehrani Fateh, Sahand Tehrani Fateh, Faezeh Shekari, Majid Mahdavi, Amir Reza Aref, Amir Reza Aref, Amir Salehi-Najafabadi, Amir Salehi-Najafabadi

    Diterbitkan 2022-04-01
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  5. 5
    Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers

    Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers oleh Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Hadi Aghajani, Afshin Bahramy, Seyed Mohammad Salar Zaheryani, Javad Behroozi, Seyyed Mohammad Kahani, Pouria Mohammadi, Masoud Garshasbi

    Diterbitkan 2023-10-01
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  6. 6
    The effects of hesperidin supplementation on cardiovascular risk factors in adults: a systematic review and dose–response meta-analysis

    The effects of hesperidin supplementation on cardiovascular risk factors in adults: a systematic review and dose–response meta-analysis oleh Atie Sadat Khorasanian, Sahand Tehrani Fateh, Fatemeh Gholami, Niloufar Rasaei, Hadis Gerami, Hadis Gerami, Sayyed Saeid Khayyatzadeh, Sayyed Saeid Khayyatzadeh, Farideh Shiraseb, Omid Asbaghi, Omid Asbaghi

    Diterbitkan 2023-07-01
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  7. 7
    Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases

    Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases oleh Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Farzad Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad-Reza Ghasemi

    Diterbitkan 2024-01-01
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  8. 8
    Identification of novel mutations in TPK1 and SLC19A3 genes in families exhibiting thiamine metabolism dysfunction syndrome

    Identification of novel mutations in TPK1 and SLC19A3 genes in families exhibiting thiamine metabolism dysfunction syndrome oleh Fatemeh Norouzi Rostami, Hossein Sadeghi, Farzad Hashemi-Gorji, Sahand Tehrani Fateh, Reza Mirfakhraie, Parvaneh Karimzadeh, Milad Davarpanah, Sanaz Jamshidi, Rasoul Madannejad, Parinaz Moghimi, Mahdis Ekrami, Mohammad Miryounesi, Mohammad-Reza Ghasemi

    Diterbitkan 2024-03-01
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  9. 9
    Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review

    Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review oleh Mohammad-Reza Ghasemi, Sahand Tehrani Fateh, Aysan Moeinafshar, Hossein Sadeghi, Parvaneh Karimzadeh, Reza Mirfakhraie, Mitra Rezaei, Farzad Hashemi-Gorji, Morteza Rezvani Kashani, Fatemehsadat Fazeli Bavandpour, Saman Bagheri, Parinaz Moghimi, Masoumeh Rostami, Rasoul Madannejad, Hassan Roudgari, Mohammad Miryounesi

    Diterbitkan 2024-02-01
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  10. 10
    Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran

    Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran oleh Sara Asgarian, Hossein Lanjanian, Shiva Rahimipour Anaraki, Farzad Hadaegh, Maryam Moazzam-Jazi, Leila Najd-Hassan-Bonab, Sajedeh Masjoudi, Asiyeh Sadat Zahedi, Maryam Zarkesh, Bita Shalbafan, Mahdi Akbarzadeh, Sahand Tehrani Fateh, Davood Khalili, Amirabbas Momenan, Narges Sarbazi, Mehdi Hedayati, Fereidoun Azizi, Maryam S. Daneshpour

    Diterbitkan 2024-08-01
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  11. 11
    The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes

    The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes oleh Mahmoud Amiri Roudbar, Seyed Milad Vahedi, Jin Jin, Mina Jahangiri, Hossein Lanjanian, Danial Habibi, Sajedeh Masjoudi, Parisa Riahi, Sahand Tehrani Fateh, Farideh Neshati, Asiyeh Sadat Zahedi, Maryam Moazzam-Jazi, Leila Najd-Hassan-Bonab, Seyedeh Fatemeh Mousavi, Sara Asgarian, Maryam Zarkesh, Mohammad Reza Moghaddas, Albert Tenesa, Anoshirvan Kazemnejad, Hassan Vahidnezhad, Hakon Hakonarson, Fereidoun Azizi, Mehdi Hedayati, Maryam Sadat Daneshpour, Mahdi Akbarzadeh

    Diterbitkan 2024-09-01
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