Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Niloofar Naderi"'
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-6 (2024)
Abstract Background Long QT syndrome (LQTS) is a cardiac channelopathy characterized by impaired myocardial repolarization that predisposes to life-threatening arrhythmias. This study aimed to elucidate the genetic basis of LQTS in an affected Irania
Externí odkaz:
https://doaj.org/article/4dd9f0aba2894789862d57753028ee8d
Autor:
Amir Ghaffari Jolfayi, Erfan Kohansal, Serwa Ghasemi, Niloofar Naderi, Mahshid Hesami, MohammadHossein MozafaryBazargany, Maryam Hosseini Moghadam, Amir Farjam Fazelifar, Majid Maleki, Samira Kalayinia
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-37 (2024)
Abstract The giant protein titin (TTN) is a sarcomeric protein that forms the myofibrillar backbone for the components of the contractile machinery which plays a crucial role in muscle disorders and cardiomyopathies. Diagnosing TTN pathogenic variant
Externí odkaz:
https://doaj.org/article/46596c2876cf453eb68b68e370b610e2
Autor:
Amir Ghaffari Jolfayi, Niloofar Naderi, Serwa Ghasemi, Alireza Salmanipour, Sara Adimi, Majid Maleki, Samira Kalayinia
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background Primary carnitine deficiency (PCD) denotes low carnitine levels with an autosomal recessive pattern of inheritance. Cardiomyopathy is the most common cardiac symptom in patients with PCD, and early diagnosis can prevent complicati
Externí odkaz:
https://doaj.org/article/8f8f56202bda48dea0593a5490d12308
Autor:
Niloofar Naderi, Neda Mohsen-Pour, Yalda Nilipour, Maryam Pourirahim, Majid Maleki, Samira Kalayinia
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background The MYH7 gene, which encodes the slow/ß-cardiac myosin heavy chain, is mutated in myosin storage myopathy (MSM). The clinical spectrum of MSM is quite heterogeneous in that it ranges from cardiomyopathies to skeletal myopathies o
Externí odkaz:
https://doaj.org/article/8b12a116693c433e8ac666d8a14ee3bf
Autor:
Golnaz Houshmand, Mohammad Javad Alemzadeh-Ansari, Saeideh Mazloumzadeh, Niloofar Naderi, Maryam Pourirahim, Katayoun Heshmatzad, Majid Maleki, Samira Kalayinia
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 15, Iss 3, Pp 168-173 (2023)
Introduction: Coronary artery disease (CAD) is the leading health complication worldwide because of its high prevalence and mortality. The association between CAD susceptibility and the rs599839 (C/T) polymorphism in the human proline and serine-rich
Externí odkaz:
https://doaj.org/article/ada3f08363b14d21ac149f14f958e959
Autor:
Avisa Tabib, Taravat Talebi, Serwa Ghasemi, Maryam Pourirahim, Niloofar Naderi, Majid Maleki, Samira Kalayinia
Publikováno v:
European Journal of Medical Research, Vol 27, Iss 1, Pp 1-16 (2022)
Abstract Background Congenital heart defects (CHDs) are the most common congenital malformations, including structural malformations in the heart and great vessels. CHD complications such as low birth weight, prematurity, pregnancy termination, morta
Externí odkaz:
https://doaj.org/article/81e4cb87de9b4d5bb69d250fdee36d66
Autor:
Katayoun Heshmatzad, Niloofar Naderi, Tannaz Masoumi, Hamidreza Pouraliakbar, Samira Kalayinia
Publikováno v:
European Journal of Medical Research, Vol 27, Iss 1, Pp 1-23 (2022)
Abstract Background Alexander disease (AxD) is a rare leukodystrophy with an autosomal dominant inheritance mode. Variants in GFAP lead to this disorder and it is classified into three distinguishable subgroups: infantile, juvenile, and adult-onset t
Externí odkaz:
https://doaj.org/article/d2c6d88c908643f38a0f019c530ddd3a
Autor:
Shiva Abbasi, Neda Mohsen-Pour, Niloofar Naderi, Shahin Rahimi, Majid Maleki, Samira Kalayinia
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 13, Iss 4, Pp 336-354 (2021)
Introduction: Congenital heart disease (CHD) is the most common congenital abnormality and the main cause of infant mortality worldwide. Some of the mutations that occur in the GATA4 gene region may result in different types of CHD. Here, we report o
Externí odkaz:
https://doaj.org/article/b453de74e76747548322e1ba4d812212
Publikováno v:
Journal of Mazandaran University of Medical Sciences, Vol 30, Iss 185, Pp 33-40 (2020)
Background and purpose: Decrease in the number of oral microorganisms leads to reduction in caries score. Bacterial therapy, such as using probiotic bacteria, is an alternative procedure in treatment of infections caused by microorganisms. The purpos
Externí odkaz:
https://doaj.org/article/6704bef089134f83b76c6d2a22977204
Autor:
Elnaz Agi, Saber Asghari, Ali Namvar, Niloofar Khairkhah, Niloofar Naderi, Ali Anvar, Alireza Azizi Saraji, Azam Bolhassani
Publikováno v:
Journal of Medical Microbiology and Infectious Diseases, Vol 8, Iss 1, Pp 1-6 (2020)
Introduction: A new pathological form of HCV named as occult HCV infection (OCI) has been recently characterized by the presence of HCV RNA in liver biopsy and/or peripheral blood mononuclear cell specimens (PBMCs) and the absence of detectable circu
Externí odkaz:
https://doaj.org/article/3f3b5b4694a94104a200d4cd0cb55f99