Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Serwa Ghasemi"'
Autor:
Hamed Hesami, Serwa Ghasemi, Golnaz Houshmand, Yalda Nilipour, Mahshid Hesami, Alireza Biglari, Shahriar Nafissi, Majid Maleki, Samira Kalayinia
Publikováno v:
BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background Limb girdle muscular dystrophies (LGMDs) constitute a heterogeneous group of neuromuscular disorders with a very variable clinical presentation and overlapping traits. The clinical symptoms of LGMD typically appear in adolescence
Externí odkaz:
https://doaj.org/article/8f548777472647cfb5bf30df13f1a719
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
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-9 (2023)
Abstract Background Dilated cardiomyopathy (DCM) is a major cause of sudden cardiac death and heart failure. Up to 50% of all DCM cases have a genetic background, with variants in over 250 genes reported in association with DCM. Whole-exome sequencin
Externí odkaz:
https://doaj.org/article/d0c758942cce462899007f16ff54b766
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
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-8 (2022)
Abstract Background Familial dilated cardiomyopathy (DCM) is a genetic heart disorder characterized by progressive heart failure and sudden cardiac death. Over 250 genes have been reported in association with DCM; nonetheless, the genetic cause of mo
Externí odkaz:
https://doaj.org/article/4715e5fba3134031bcc008c6b88c3ed7
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 11, Iss 4, Pp 287-299 (2019)
Introduction: Congenital heart disease (CHD) affects 1% to 2 % of live births. The Nkx2-5 gene, is known as the significant heart marker during embryonic evolution and it is also necessary for the survival of cardiomyocytes and homeostasis in adultho
Externí odkaz:
https://doaj.org/article/55a12807975542439f2ee3ab2b3348f9
Publikováno v:
Acta Medica Iranica, Vol 58, Iss 8 (2020)
Coronary artery disease (CAD) is a common multifactorial disease with a high rate of morbidity and mortality worldwide. The MEF2A gene transcription factor belongs to the myocyte enhancer factor-2 (MEF2) family and is involved in critical processes s
Externí odkaz:
https://doaj.org/article/8908e9c4cdfa42819992b96628f2f108
Autor:
Mohammad Mahdavi, Neda Mohsen-Pour, Majid Maleki, Serwa Ghasemi, Avisa Tabib, Golnaz Houshmand, Niloofar Naderi, Tannaz Masoumi, Hamidreza Pouraliakbar, Samira Kalayinia
Publikováno v:
Laboratory Medicine.
Objective We studied the clinical and molecular features of a family with hypertrophic cardiomyopathy (HCM). Background A very heterogeneous disease affecting the heart muscle, HCM is mostly caused by variants in the proteins of sarcomeres. The detec
Autor:
Katayoun Heshmatzad, Niloofar Naderi, Majid Maleki, Shiva Abbasi, Serwa Ghasemi, Nooshin Ashrafi, Amir Farjam Fazelifar, Mohammad Mahdavi, Samira Kalayinia
Publikováno v:
Journal of Cellular and Molecular Medicine.