Showing 1 - 7 results of 7 for search 'Maryam Pourirahim', query time: 0.03s Refine Results
  1. 1
    A novel stop-gain pathogenic variant in the KCNQ1 gene causing long QT syndrome 1

    A novel stop-gain pathogenic variant in the KCNQ1 gene causing long QT syndrome 1 by Samira Kalayinia, Mohammad Dalili, Maryam Pourirahim, Majid Maleki, Nejat Mahdieh

    Published 2023-01-01
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  2. 2
    Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac death

    Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac death by Amir Azimi, Maryam Pourirahim, Golnaz Houshmand, Sara Adimi, Majid Maleki, Samira Kalayinia

    Published 2023-10-01
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  3. 3
    Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathy

    Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathy by Samira Kalayinia, Mohammad Mahdavi, Golnaz Houshmand, Mahshid Hesami, Maryam Pourirahim, Majid Maleki

    Published 2022-08-01
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  4. 4
    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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  5. 5
    Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing

    Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing by Amir Farjam Fazelifar, Maryam Pourirahim, Tannaz Masoumi, Alireza Biglari, Majid Maleki, Samira Kalayinia

    Published 2023-06-01
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  6. 6
    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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  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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