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Samira Kalayinia

Showing results (21-30 of 53) with videos related to

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Molecular Genetics & Genomic Medicine|June 8, 2026
MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular TachycardiaSamira Kalayinia, Tannaz Masoumi, Amirreza Taherkhani, et al.
BMC Cardiovascular Disorders|February 12, 2022
Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillationMahshid Malakootian, Masoumeh Jalilian, Samira Kalayinia, et al.
Journal of Arrhythmia|June 16, 2023
Identification of a novel pathogenic variant in <i>KCNH2</i> in an Iranian family with long QT syndrome 2 by whole-exome sequencingAmir Farjam Fazelifar, Maryam Pourirahim, Tannaz Masoumi, et al.
Laboratory Medicine|June 10, 2022
Whole-Exome Sequencing Revealed a Pathogenic Nonsense Variant in the SLC19A2 Gene in an Iranian Family with Thiamine-Responsive Megaloblastic AnemiaNeda Mohsen-Pour, Niloofar Naderi, Serwa Ghasemi, et al.
BMC Cardiovascular Disorders|October 4, 2023
A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathyNiloofar Naderi, Neda Mohsen-Pour, Yalda Nilipour, et al.
Journal of Cardiovascular and Thoracic Research|January 20, 2022
<i>In silico</i> analysis of <i>GATA4</i> variants demonstrates main contribution to congenital heart diseaseShiva Abbasi, Neda Mohsen-Pour, Niloofar Naderi, et al.
European Journal of Medical Research|December 10, 2022
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defectsAvisa Tabib, Taravat Talebi, Serwa Ghasemi, et al.
Gene|November 23, 2023
Catecholaminergic polymorphic ventricular tachycardia (and seizure) caused by a novel homozygous likely pathogenic variant in CASQ2 geneAmir Askarinejad, Shiva Esmaeili, Mohamad Dalili, et al.
Current Molecular Medicine|August 9, 2021
Chromosome 9 Inversion: Pathogenic or Benign? A Comprehensive Systematic Review of all Clinical ReportsNeda Mohsen-Pour, Taravat Talebi, Niloofar Naderi, et al.
ESC Heart Failure|February 8, 2024
A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weaknessMohammadHossein MozafaryBazargany, Shiva Esmaeili, Mahshid Hesami, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Molecular Genetics & Genomic Medicine|June 8, 2026
MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular TachycardiaSamira Kalayinia, Tannaz Masoumi, Amirreza Taherkhani, et al.
BMC Cardiovascular Disorders|February 12, 2022
Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillationMahshid Malakootian, Masoumeh Jalilian, Samira Kalayinia, et al.
Journal of Arrhythmia|June 16, 2023
Identification of a novel pathogenic variant in <i>KCNH2</i> in an Iranian family with long QT syndrome 2 by whole-exome sequencingAmir Farjam Fazelifar, Maryam Pourirahim, Tannaz Masoumi, et al.
Laboratory Medicine|June 10, 2022
Whole-Exome Sequencing Revealed a Pathogenic Nonsense Variant in the SLC19A2 Gene in an Iranian Family with Thiamine-Responsive Megaloblastic AnemiaNeda Mohsen-Pour, Niloofar Naderi, Serwa Ghasemi, et al.
BMC Cardiovascular Disorders|October 4, 2023
A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathyNiloofar Naderi, Neda Mohsen-Pour, Yalda Nilipour, et al.
Journal of Cardiovascular and Thoracic Research|January 20, 2022
<i>In silico</i> analysis of <i>GATA4</i> variants demonstrates main contribution to congenital heart diseaseShiva Abbasi, Neda Mohsen-Pour, Niloofar Naderi, et al.
European Journal of Medical Research|December 10, 2022
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defectsAvisa Tabib, Taravat Talebi, Serwa Ghasemi, et al.
Gene|November 23, 2023
Catecholaminergic polymorphic ventricular tachycardia (and seizure) caused by a novel homozygous likely pathogenic variant in CASQ2 geneAmir Askarinejad, Shiva Esmaeili, Mohamad Dalili, et al.
Current Molecular Medicine|August 9, 2021
Chromosome 9 Inversion: Pathogenic or Benign? A Comprehensive Systematic Review of all Clinical ReportsNeda Mohsen-Pour, Taravat Talebi, Niloofar Naderi, et al.
ESC Heart Failure|February 8, 2024
A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weaknessMohammadHossein MozafaryBazargany, Shiva Esmaeili, Mahshid Hesami, et al.
Pageof 6