Search research articles
Contact Us
Filters
Showing results (21-30 of 32) with videos related to
Page
of 4
Sort By:
The Egyptian Heart Journal : (EHJ) : Official Bulletin of the Egyptian Society of Cardiology
|
April 16, 2025
Evaluation of dyssynchrony in children with dilated cardiomyopathy: a comparison of electrical and mechanical delay using Doppler, tissue imaging and strain
Fariba Rashidi Ghader, Mohammad Mahdavi, Hossein Mehrali, et al.
American Journal of Medical Genetics. Part A
|
August 20, 2021
Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome
Bahareh Rabbani, Mohammadrafi Khorgami, Mohammad Dalili, et al.
Research in Cardiovascular Medicine
|
March 20, 2015
Single Dose Corticosteroid Therapy After Surgical Repair of Fallot's Tetralogy; A Randomized Controlled Clinical Trial
Mohammad Dalili, Ahmad Vesal, Avisa Tabib, et al.
Pediatric Cardiology
|
October 21, 2024
The Influence of Arrhythmia on the Outcomes of Pediatric Patients with Idiopathic Dilated Cardiomyopathy
Mohammad Dalili, Marieh Dastafshan, Mohammad Mahdavi, et al.
Journal of Electrocardiology
|
October 17, 2017
Identification and characterization of a novel recessive KCNQ1 mutation associated with Romano-Ward Long-QT syndrome in two Iranian families
Zahra Zafari, Mohammad Dalili, Sirus Zeinali, 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 Syndrome
Samira Kalayinia, Amir Ghaffari Jolfayi, Amirali Soheili, et al.
Iranian Biomedical Journal
|
February 25, 2019
Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families
Azam Amirian, Zahra Zafari, Morteza Karimipoor, et al.
Iranian Journal of Basic Medical Sciences
|
January 27, 2018
Novel frameshift mutation in the <i>KCNQ1</i> gene responsible for Jervell and Lange-Nielsen syndrome
Azam Amirian, Seyed Mohammad Dalili, Zahra Zafari, et al.
Acta Medica Iranica
|
May 21, 2011
Growth status of Iranian children with hemodynamically important congenital heart disease
Mohammad Dalili, Seyed Mahmood Meraji, Paridokht Davari, et al.
Journal of Arrhythmia
|
June 29, 2018
Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families
Azam Amirian, Zahra Zafari, Mohammad Dalili, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
The Egyptian Heart Journal : (EHJ) : Official Bulletin of the Egyptian Society of Cardiology
|
April 16, 2025
Evaluation of dyssynchrony in children with dilated cardiomyopathy: a comparison of electrical and mechanical delay using Doppler, tissue imaging and strain
Fariba Rashidi Ghader, Mohammad Mahdavi, Hossein Mehrali, et al.
American Journal of Medical Genetics. Part A
|
August 20, 2021
Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome
Bahareh Rabbani, Mohammadrafi Khorgami, Mohammad Dalili, et al.
Research in Cardiovascular Medicine
|
March 20, 2015
Single Dose Corticosteroid Therapy After Surgical Repair of Fallot's Tetralogy; A Randomized Controlled Clinical Trial
Mohammad Dalili, Ahmad Vesal, Avisa Tabib, et al.
Pediatric Cardiology
|
October 21, 2024
The Influence of Arrhythmia on the Outcomes of Pediatric Patients with Idiopathic Dilated Cardiomyopathy
Mohammad Dalili, Marieh Dastafshan, Mohammad Mahdavi, et al.
Journal of Electrocardiology
|
October 17, 2017
Identification and characterization of a novel recessive KCNQ1 mutation associated with Romano-Ward Long-QT syndrome in two Iranian families
Zahra Zafari, Mohammad Dalili, Sirus Zeinali, 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 Syndrome
Samira Kalayinia, Amir Ghaffari Jolfayi, Amirali Soheili, et al.
Iranian Biomedical Journal
|
February 25, 2019
Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families
Azam Amirian, Zahra Zafari, Morteza Karimipoor, et al.
Iranian Journal of Basic Medical Sciences
|
January 27, 2018
Novel frameshift mutation in the <i>KCNQ1</i> gene responsible for Jervell and Lange-Nielsen syndrome
Azam Amirian, Seyed Mohammad Dalili, Zahra Zafari, et al.
Acta Medica Iranica
|
May 21, 2011
Growth status of Iranian children with hemodynamically important congenital heart disease
Mohammad Dalili, Seyed Mahmood Meraji, Paridokht Davari, et al.
Journal of Arrhythmia
|
June 29, 2018
Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families
Azam Amirian, Zahra Zafari, Mohammad Dalili, et al.
Page
of 4