Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mohammad Reza Samienasab"'
Autor:
Mahshid Givi, Nizal Sarrafzadegan, Mohammad Garakyaraghi, Ghasem Yadegarfar, Masoumeh Sadeghi, Alireza Khosravi, Amir Hossein Azhari, Mohammad Reza Samienasab, Davood Shafie, Mohammad Saadatnia, Hamidreza Roohafza, Navid Paydari, Azam Soleimani, Mohsen Hosseinzadeh, Seyed Abdullah Ahmadi, Leila Dehghani, Jamshid Najafian, Elham Andalib, Javad Shahabi, Mohammad Reza Sabri
Publikováno v:
ARYA Atherosclerosis, Vol 13, Iss 5, Pp 236-244 (2017)
BACKGROUND: Our aim was to create and establish a database called “Persian Registry Of cardioVascular diseasE (PROVE)” in order to be used for future research and in addition, as a tool to develop national guidelines for diagnosis, treatment, and
Externí odkaz:
https://doaj.org/article/d726e95f4b974291b8bf5d3e95902dd7
Publikováno v:
Advanced Biomedical Research, Vol 6, Iss 1, Pp 32-32 (2017)
Background: Mutations in different genes including dystrophin-associated glycoprotein complex caused familial dilated cardiomyopathy which is a genetically heterogeneous disease. The δ-SG gene contains nine exons spanning a 433-kb region of genomic
Externí odkaz:
https://doaj.org/article/87517c6bd18b4d47ac0f0aa41d2a560d
Genetic analysis of Iranian family with hereditary cardiac arrhythmias by next generation sequencing
Autor:
Marzieh Asadi, Roger Foo, Mohammad Reza Samienasab, Ahmad Reza Salehi, Majid Kheirollahi, Hossein Khanahmad, Rasoul Salehi
Publikováno v:
Advanced Biomedical Research, Vol 5, Iss 1, Pp 55-55 (2016)
Background: Cardiac arrhythmias are responsible for several cases of syncope and sudden cardiac death annually worldwide. Due to overlapping clinical symptoms in some cardiac arrhythmias genetic studies would help to confirm the primary clinical diag
Externí odkaz:
https://doaj.org/article/e4bc69ca822b4435929cbec1e6ec4336
Autor:
Marzi Asadi, Zahurul A. Bhuiyan, Ahmad Reza Salehi, Mohammad Reza Samienasab, Rasoul Salehi, Roger Foo, Shahab Shahrzad
Publikováno v:
Anatolian journal of cardiology, vol. 16, no. 3, pp. 170-174
Anatolian Journal of Cardiology
Anatolian Journal of Cardiology
Objective: SCN5A encodes alpha subunit of the major sodium channel (Nav1.5) in human cardiac tissue. Malfunction of this cardiac sodium channel is associated with a variety of cardiac arrhythmias and myocardial inherited diseases. Methods: Fifty-thre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::681d9000b6dd76a242ec76dc1c5a8105
https://doi.org/10.5152/akd.2015.6060
https://doi.org/10.5152/akd.2015.6060
Genetic analysis of Iranian family with hereditary cardiac arrhythmias by next generation sequencing
Autor:
Mohammad Reza Samienasab, Ahmad Reza Salehi, Roger Foo, Majid Kheirollahi, Marzieh Asadi, Rasoul Salehi, Hossein Khanahmad
Publikováno v:
Advanced Biomedical Research
Advanced Biomedical Research, Vol 5, Iss 1, Pp 55-55 (2016)
Advanced Biomedical Research, Vol 5, Iss 1, Pp 55-55 (2016)
Background: Cardiac arrhythmias are responsible for several cases of syncope and sudden cardiac death annually worldwide. Due to overlapping clinical symptoms in some cardiac arrhythmias genetic studies would help to confirm the primary clinical diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e18b7868cc8be98b717f97cf9c938c6d
https://pubmed.ncbi.nlm.nih.gov/27110552
https://pubmed.ncbi.nlm.nih.gov/27110552
Publikováno v:
Advanced Biomedical Research
Advanced Biomedical Research, Vol 6, Iss 1, Pp 32-32 (2017)
Advanced Biomedical Research, Vol 6, Iss 1, Pp 32-32 (2017)
Background: Mutations in different genes including dystrophin-associated glycoprotein complex caused familial dilated cardiomyopathy which is a genetically heterogeneous disease. The δ-SG gene contains nine exons spanning a 433-kb region of genomic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f659e452e17a2da397c8935217bfcab
https://doi.org/10.4103/2277-9175.188492
https://doi.org/10.4103/2277-9175.188492