Showing 1 - 8 results of 8 for search 'Niloofar Naderi', query time: 0.03s Refine Results
  1. 1
    Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing

    Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing by Katayoun Heshmatzad, Niloofar Naderi, Tannaz Masoumi, Hamidreza Pouraliakbar, Samira Kalayinia

    Published 2022-09-01
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  2. 2
    Comparing the Effect of Probiotic and Non-probiotic Yogurt Drinks on Two Common Oral Microorganisms: An In Vitro Study

    Comparing the Effect of Probiotic and Non-probiotic Yogurt Drinks on Two Common Oral Microorganisms: An In Vitro Study by Arezoo Rayani, Mohammad Ahanjan, Hamid Reza Goli, Niloofar Naderi fard, Maryam zamanzdeah

    Published 2020-05-01
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  3. 3
    A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy

    A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy by Niloofar Naderi, Neda Mohsen-Pour, Yalda Nilipour, Maryam Pourirahim, Majid Maleki, Samira Kalayinia

    Published 2023-10-01
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  4. 4
    In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease

    In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease by Shiva Abbasi, Neda Mohsen-Pour, Niloofar Naderi, Shahin Rahimi, Majid Maleki, Samira Kalayinia

    Published 2021-12-01
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  5. 5
    A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects

    A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects by Avisa Tabib, Taravat Talebi, Serwa Ghasemi, Maryam Pourirahim, Niloofar Naderi, Majid Maleki, Samira Kalayinia

    Published 2022-12-01
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  6. 6
    A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features

    A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features by Amir Ghaffari Jolfayi, Niloofar Naderi, Serwa Ghasemi, Alireza Salmanipour, Sara Adimi, Majid Maleki, Samira Kalayinia

    Published 2024-01-01
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  7. 7
    Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population

    Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population by Golnaz Houshmand, Mohammad Javad Alemzadeh-Ansari, Saeideh Mazloumzadeh, Niloofar Naderi, Maryam Pourirahim, Katayoun Heshmatzad, Majid Maleki, Samira Kalayinia

    Published 2023-09-01
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  8. 8
    Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies

    Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies by Amir Ghaffari Jolfayi, Erfan Kohansal, Serwa Ghasemi, Niloofar Naderi, Mahshid Hesami, MohammadHossein MozafaryBazargany, Maryam Hosseini Moghadam, Amir Farjam Fazelifar, Majid Maleki, Samira Kalayinia

    Published 2024-03-01
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