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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 approaches
Mohammadrafie 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 disease
Samira 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 Fallot
Samira 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 disease
Samira 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 cardiomyopathy
Tannaz Masoumi, Hamed Hesami, Majid Maleki, et al.
Annals of Medicine
|
October 14, 2017
Next generation sequencing applications for cardiovascular disease
Samira 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 sequencing
Katayoun 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 Cardiomyopathy
Maryam 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 1
Samira Kalayinia, Mohammad Dalili, Maryam Pourirahim, et al.
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Search research articles
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Showing results (1-10 of 53) with videos related to
Sort By:
Page
of 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 approaches
Mohammadrafie 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 disease
Samira 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 Fallot
Samira 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 disease
Samira 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 cardiomyopathy
Tannaz Masoumi, Hamed Hesami, Majid Maleki, et al.
Annals of Medicine
|
October 14, 2017
Next generation sequencing applications for cardiovascular disease
Samira 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 sequencing
Katayoun 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 Cardiomyopathy
Maryam 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 1
Samira Kalayinia, Mohammad Dalili, Maryam Pourirahim, et al.
Page
of 6