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Samira Kalayinia

Showing results (1-10 of 53) with videos related to

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International Journal of Emergency Medicine|February 10, 2025
Primary diagnosis of atrioventricular pseudo-block in a neonate with definitive diagnosis of long QT syndrome: diagnostic considerations and therapeutic approachesMohammadrafie Khorgami, Fatemeh Naderi, Samira Kalayinia
Journal of Cardiovascular and Thoracic Research|December 12, 2019
A comprehensive in silico analysis, distribution and frequency of human <i>Nkx2-5</i> mutations; A critical gene in congenital heart diseaseSamira Kalayinia, Serwa Ghasemi, Nejat Mahdieh
Laboratory Medicine|May 4, 2021
Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of FallotSamira Kalayinia, Majid Maleki, Mohammad Mahdavi, et al.
Journal of Clinical Laboratory Analysis|December 24, 2019
A novel de novo dominant mutation of NOTCH1 gene in an Iranian family with non-syndromic congenital heart diseaseSamira Kalayinia, Majid Maleki, Mohammad Mahdavi, et al.
BMC Medical Genomics|April 30, 2025
Exploring the c.406 C > T variant in TNNI3 gene: pathogenic insights into restrictive cardiomyopathyTannaz Masoumi, Hamed Hesami, Majid Maleki, et al.
Annals of Medicine|October 14, 2017
Next generation sequencing applications for cardiovascular diseaseSamira Kalayinia, Hamidreza Goodarzynejad, Majid Maleki, et al.
European Journal of Medical Research|September 10, 2022
Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencingKatayoun Heshmatzad, Niloofar Naderi, Tannaz Masoumi, et al.
BMC Cardiovascular Disorders|April 23, 2024
Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic CardiomyopathyMaryam Pourirahim, Golnaz Houshmand, Leyla Abdolkarimi, et al.
International Journal of Endocrinology|December 23, 2021
An Iranian Congenital Adrenal Hypoplasia Patient with Elevated Testosterone in Infancy due to a Novel Pathogenic Frameshift Variant in <i>NR0B1</i>Samira Kalayinia, Saeed Talebi, Mohammad Miryounesi, et al.
European Journal of Medical Research|January 12, 2023
A novel stop-gain pathogenic variant in the KCNQ1 gene causing long QT syndrome 1Samira Kalayinia, Mohammad Dalili, Maryam Pourirahim, et al.
Pageof 6

Showing results (1-10 of 53) with videos related to

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Pageof 6
International Journal of Emergency Medicine|February 10, 2025
Primary diagnosis of atrioventricular pseudo-block in a neonate with definitive diagnosis of long QT syndrome: diagnostic considerations and therapeutic approachesMohammadrafie Khorgami, Fatemeh Naderi, Samira Kalayinia
Journal of Cardiovascular and Thoracic Research|December 12, 2019
A comprehensive in silico analysis, distribution and frequency of human <i>Nkx2-5</i> mutations; A critical gene in congenital heart diseaseSamira Kalayinia, Serwa Ghasemi, Nejat Mahdieh
Laboratory Medicine|May 4, 2021
Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of FallotSamira Kalayinia, Majid Maleki, Mohammad Mahdavi, et al.
Journal of Clinical Laboratory Analysis|December 24, 2019
A novel de novo dominant mutation of NOTCH1 gene in an Iranian family with non-syndromic congenital heart diseaseSamira Kalayinia, Majid Maleki, Mohammad Mahdavi, et al.
BMC Medical Genomics|April 30, 2025
Exploring the c.406 C > T variant in TNNI3 gene: pathogenic insights into restrictive cardiomyopathyTannaz Masoumi, Hamed Hesami, Majid Maleki, et al.
Annals of Medicine|October 14, 2017
Next generation sequencing applications for cardiovascular diseaseSamira Kalayinia, Hamidreza Goodarzynejad, Majid Maleki, et al.
European Journal of Medical Research|September 10, 2022
Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencingKatayoun Heshmatzad, Niloofar Naderi, Tannaz Masoumi, et al.
BMC Cardiovascular Disorders|April 23, 2024
Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic CardiomyopathyMaryam Pourirahim, Golnaz Houshmand, Leyla Abdolkarimi, et al.
International Journal of Endocrinology|December 23, 2021
An Iranian Congenital Adrenal Hypoplasia Patient with Elevated Testosterone in Infancy due to a Novel Pathogenic Frameshift Variant in <i>NR0B1</i>Samira Kalayinia, Saeed Talebi, Mohammad Miryounesi, et al.
European Journal of Medical Research|January 12, 2023
A novel stop-gain pathogenic variant in the KCNQ1 gene causing long QT syndrome 1Samira Kalayinia, Mohammad Dalili, Maryam Pourirahim, et al.
Pageof 6