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Majid Maleki

Showing results (41-50 of 170) with videos related to

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BMC Medical Genomics|May 7, 2024
Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencingErfan Kohansal, Niloofar Naderi, Amir Farjam Fazelifar, et al.
Global Journal of Health Science|January 13, 2016
A Review of Visiting Policies in Intensive Care UnitsShiva Khaleghparast, Soodabeh Joolaee, Behrooz Ghanbari, et al.
Nursing Ethics|May 9, 2017
New visiting policy: A step toward nursing ethicsShiva Khaleghparast, Soodabeh Joolaee, Majid Maleki, et al.
Medical Journal of the Islamic Republic of Iran|July 7, 2018
A novel <i>PKP2</i> mutation and intrafamilial phenotypic variability in ARVC/DNejat Mahdieh, Sedigheh Saedi, Mahdieh Soveizi, et al.
ESC Heart Failure|July 1, 2020
Cardio-oncology discipline: focus on the necessities in developing countriesAzin Alizadehasl, Ahmad Amin, Majid Maleki, et al.
Research in Cardiovascular Medicine|December 6, 2014
Normal reference values of tissue Doppler imaging parameters for right ventricular function in young adults: a population based studyMaryam Shojaeifard, Maryam Esmaeilzadeh, Majid Maleki, et al.
Research in Cardiovascular Medicine|December 6, 2014
Insulin resistance in pulmonary arterial hypertension, is it a novel disease modifier?Nasim Naderi, Pedram Boobejame, Hooman Bakhshandeh, et al.
BMC Medical Genomics|October 27, 2023
Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac deathAmir Azimi, Maryam Pourirahim, Golnaz Houshmand, et al.
BMC Cardiovascular Disorders|August 6, 2022
Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathySamira Kalayinia, Mohammad Mahdavi, Golnaz Houshmand, et al.
Cardiology Research and Practice|November 19, 2025
Unlocking the Secrets of Andersen-Tawil Syndrome: The Role of Next-Generation Sequencing in a Family With Long QT SyndromeMansoor Namazi, Niloofar Naderi, Amir Askarinejad, et al.
Pageof 17

Showing results (41-50 of 170) with videos related to

Sort By:
Pageof 17
BMC Medical Genomics|May 7, 2024
Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencingErfan Kohansal, Niloofar Naderi, Amir Farjam Fazelifar, et al.
Global Journal of Health Science|January 13, 2016
A Review of Visiting Policies in Intensive Care UnitsShiva Khaleghparast, Soodabeh Joolaee, Behrooz Ghanbari, et al.
Nursing Ethics|May 9, 2017
New visiting policy: A step toward nursing ethicsShiva Khaleghparast, Soodabeh Joolaee, Majid Maleki, et al.
Medical Journal of the Islamic Republic of Iran|July 7, 2018
A novel <i>PKP2</i> mutation and intrafamilial phenotypic variability in ARVC/DNejat Mahdieh, Sedigheh Saedi, Mahdieh Soveizi, et al.
ESC Heart Failure|July 1, 2020
Cardio-oncology discipline: focus on the necessities in developing countriesAzin Alizadehasl, Ahmad Amin, Majid Maleki, et al.
Research in Cardiovascular Medicine|December 6, 2014
Normal reference values of tissue Doppler imaging parameters for right ventricular function in young adults: a population based studyMaryam Shojaeifard, Maryam Esmaeilzadeh, Majid Maleki, et al.
Research in Cardiovascular Medicine|December 6, 2014
Insulin resistance in pulmonary arterial hypertension, is it a novel disease modifier?Nasim Naderi, Pedram Boobejame, Hooman Bakhshandeh, et al.
BMC Medical Genomics|October 27, 2023
Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac deathAmir Azimi, Maryam Pourirahim, Golnaz Houshmand, et al.
BMC Cardiovascular Disorders|August 6, 2022
Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathySamira Kalayinia, Mohammad Mahdavi, Golnaz Houshmand, et al.
Cardiology Research and Practice|November 19, 2025
Unlocking the Secrets of Andersen-Tawil Syndrome: The Role of Next-Generation Sequencing in a Family With Long QT SyndromeMansoor Namazi, Niloofar Naderi, Amir Askarinejad, et al.
Pageof 17