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Samira Kalayinia

Showing results (31-40 of 53) with videos related to

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BMC Medical Genomics|May 8, 2022
Dilated cardiomyopathy caused by a pathogenic nucleotide variant in RBM20 in an Iranian familyMahshid Malakootian, Mahrokh Bagheri Moghaddam, Samira Kalayinia, et al.
ESC Heart Failure|June 14, 2024
Identification of a novel likely pathogenic TPM1 variant linked to hypertrophic cardiomyopathy in a family with sudden cardiac deathAmir Azimi, Mahdieh Soveizi, Alireza Salmanipour, et al.
The Indian Journal of Medical Research|June 1, 2016
Extracellular matrix protein 1 gene (ECM1) mutations in nine Iranian families with lipoid proteinosisFarzad Izadi, Frouzandeh Mahjoubi, Mohammad Farhadi, et al.
Cardiology Research and Practice|September 5, 2025
Beyond the Beat, Next-Generation Sequencing Discovery of Novel <i>RYR2</i> Gene Variant in Long QT SyndromeSamira Kalayinia, Amir Ghaffari Jolfayi, Amirali Soheili, et al.
Journal of Clinical Laboratory Analysis|September 28, 2018
Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case reportSamira Kalayinia, Tina Shahani, Alireza Biglari, et al.
BMC Cardiovascular Disorders|January 3, 2024
A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy featuresAmir Ghaffari Jolfayi, Niloofar Naderi, Serwa Ghasemi, et al.
Laboratory Medicine|December 19, 2023
Whole-exome sequencing uncovers a novel EFEMP2 gene variant (c.C247T) associated with dominant nonsyndromic thoracic aortic aneurysmParham Sadeghipour, Marzieh Valuian, Serwa Ghasemi, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|August 14, 2023
Prediction of Parkinson's disease pathogenic variants using hybrid Machine learning systems and radiomic featuresGhasem Hajianfar, Samira Kalayinia, Mahdi Hosseinzadeh, et al.
Coronary Artery Disease|February 4, 2014
Association between the atrial natriuretic peptide rs5065 gene polymorphism and the presence and severity of coronary artery disease in an Iranian populationShayan Ziaee, Samira Kalayinia, Mohammad A Boroumand, et al.
Journal of Clinical Laboratory Analysis|May 23, 2019
GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart diseaseSamira Kalayinia, Majid Maleki, Hassan Rokni-Zadeh, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
BMC Medical Genomics|May 8, 2022
Dilated cardiomyopathy caused by a pathogenic nucleotide variant in RBM20 in an Iranian familyMahshid Malakootian, Mahrokh Bagheri Moghaddam, Samira Kalayinia, et al.
ESC Heart Failure|June 14, 2024
Identification of a novel likely pathogenic TPM1 variant linked to hypertrophic cardiomyopathy in a family with sudden cardiac deathAmir Azimi, Mahdieh Soveizi, Alireza Salmanipour, et al.
The Indian Journal of Medical Research|June 1, 2016
Extracellular matrix protein 1 gene (ECM1) mutations in nine Iranian families with lipoid proteinosisFarzad Izadi, Frouzandeh Mahjoubi, Mohammad Farhadi, et al.
Cardiology Research and Practice|September 5, 2025
Beyond the Beat, Next-Generation Sequencing Discovery of Novel <i>RYR2</i> Gene Variant in Long QT SyndromeSamira Kalayinia, Amir Ghaffari Jolfayi, Amirali Soheili, et al.
Journal of Clinical Laboratory Analysis|September 28, 2018
Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case reportSamira Kalayinia, Tina Shahani, Alireza Biglari, et al.
BMC Cardiovascular Disorders|January 3, 2024
A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy featuresAmir Ghaffari Jolfayi, Niloofar Naderi, Serwa Ghasemi, et al.
Laboratory Medicine|December 19, 2023
Whole-exome sequencing uncovers a novel EFEMP2 gene variant (c.C247T) associated with dominant nonsyndromic thoracic aortic aneurysmParham Sadeghipour, Marzieh Valuian, Serwa Ghasemi, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|August 14, 2023
Prediction of Parkinson's disease pathogenic variants using hybrid Machine learning systems and radiomic featuresGhasem Hajianfar, Samira Kalayinia, Mahdi Hosseinzadeh, et al.
Coronary Artery Disease|February 4, 2014
Association between the atrial natriuretic peptide rs5065 gene polymorphism and the presence and severity of coronary artery disease in an Iranian populationShayan Ziaee, Samira Kalayinia, Mohammad A Boroumand, et al.
Journal of Clinical Laboratory Analysis|May 23, 2019
GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart diseaseSamira Kalayinia, Majid Maleki, Hassan Rokni-Zadeh, et al.
Pageof 6