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Dimensions of Critical Care Nursing : DCCN
|
April 5, 2017
Patients' and Families' Satisfaction With Visiting Policies in Cardiac Intensive Care Units
Shiva Khaleghparast, Soodabeh Joolaee, Majid Maleki, et al.
European Journal of Echocardiography : the Journal of the Working Group on Echocardiography of the European Society of Cardiology
|
August 29, 2006
Cardiac cavernous hemangioma
Maryam Esmaeilzadeh, Rozita Jalalian, Majid Maleki, et al.
Congestive Heart Failure (Greenwich, Conn.)
|
November 23, 2011
Pulmonary arterial elastance for estimating right ventricular afterload in systolic heart failure
Ahmad Amin, Sepideh Taghavi, Maryam Esmaeilzadeh, et al.
Cardiology Journal
|
October 9, 2012
Pheochromocytoma-induced reverse tako-tsubo with rapid recovery of left ventricular function
Nasim Naderi, Ahmad Amin, Ali Setayesh, et al.
Genetics Research
|
December 11, 2023
Genetic Variations in the Human Angiotensin-ConvertingEnzyme 2 and Susceptibility to Coronavirus Disease-19
Taravat Talebi, Tannaz Masoumi, Katayoun Heshmatzad, et al.
Molecular Genetics & Genomic Medicine
|
June 8, 2026
MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular Tachycardia
Samira Kalayinia, Tannaz Masoumi, Amirreza Taherkhani, et al.
Research in Cardiovascular Medicine
|
December 6, 2014
Development and Validation of the First Iranian Questionnaire to Assess Quality of Life in Patients With Heart Failure: IHF-QoL
Nasim Naderi, Hooman Bakhshandeh, Ahmad Amin, et al.
Archives of Medical Research
|
November 3, 2019
Modulatory Role of SIRT1 and Resistin as Therapeutic Targets in Patients with Aortic Valve Stenosis
Niloufar Samiei, Saeid Hosseini, Majid Maleki, 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 sequencing
Amir 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 Anemia
Neda Mohsen-Pour, Niloofar Naderi, Serwa Ghasemi, et al.
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of 17
Search research articles
Search
Showing results (51-60 of 170) with videos related to
Sort By:
Page
of 17
Dimensions of Critical Care Nursing : DCCN
|
April 5, 2017
Patients' and Families' Satisfaction With Visiting Policies in Cardiac Intensive Care Units
Shiva Khaleghparast, Soodabeh Joolaee, Majid Maleki, et al.
European Journal of Echocardiography : the Journal of the Working Group on Echocardiography of the European Society of Cardiology
|
August 29, 2006
Cardiac cavernous hemangioma
Maryam Esmaeilzadeh, Rozita Jalalian, Majid Maleki, et al.
Congestive Heart Failure (Greenwich, Conn.)
|
November 23, 2011
Pulmonary arterial elastance for estimating right ventricular afterload in systolic heart failure
Ahmad Amin, Sepideh Taghavi, Maryam Esmaeilzadeh, et al.
Cardiology Journal
|
October 9, 2012
Pheochromocytoma-induced reverse tako-tsubo with rapid recovery of left ventricular function
Nasim Naderi, Ahmad Amin, Ali Setayesh, et al.
Genetics Research
|
December 11, 2023
Genetic Variations in the Human Angiotensin-ConvertingEnzyme 2 and Susceptibility to Coronavirus Disease-19
Taravat Talebi, Tannaz Masoumi, Katayoun Heshmatzad, et al.
Molecular Genetics & Genomic Medicine
|
June 8, 2026
MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular Tachycardia
Samira Kalayinia, Tannaz Masoumi, Amirreza Taherkhani, et al.
Research in Cardiovascular Medicine
|
December 6, 2014
Development and Validation of the First Iranian Questionnaire to Assess Quality of Life in Patients With Heart Failure: IHF-QoL
Nasim Naderi, Hooman Bakhshandeh, Ahmad Amin, et al.
Archives of Medical Research
|
November 3, 2019
Modulatory Role of SIRT1 and Resistin as Therapeutic Targets in Patients with Aortic Valve Stenosis
Niloufar Samiei, Saeid Hosseini, Majid Maleki, 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 sequencing
Amir 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 Anemia
Neda Mohsen-Pour, Niloofar Naderi, Serwa Ghasemi, et al.
Page
of 17