Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Maryam Aliramezany"'
Autor:
Maryam Aliramezany
Publikováno v:
Journal of Mazandaran University of Medical Sciences, Vol 34, Iss 232, Pp 191-203 (2024)
Background and purpose: Considering the progress made in the field of diagnosis and treatment of heart diseases, one of the heart diseases that has a high prevalence today is congenital heart disease. These people have their own special needs because
Externí odkaz:
https://doaj.org/article/ef8209e202f648be9f051205dadd0772
Autor:
Zahra Khajali, Nasibeh Mohammadi, Yaser Toloueitabar, Majid Maleki, Sedigheh Saedi, Zeinab Norouzi, Saeedeh Mazloum-Zadeh, Maryam Chenaghlou, Amirhossein Jalali, Hassan Tatari, Maryam Aliramezany
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 18, Iss 1, Pp 1-6 (2023)
Abstract Objectives Tetralogy of Fallot (TOF) is a common congenital heart disease which should be corrected. The recommended time for the Tetralogy of Fallot Total Correction (TFTC) surgery is during the infancy for the possible difficulties during
Externí odkaz:
https://doaj.org/article/47d38420e8424178a16754a16fe37edc
Autor:
Zahra Khajali, Nasibeh Mohammadi, Yaser Toloueitabar, Majid Maleki, Sedigheh Saedi, Zeinab nourouzi, Saeideh Mazloum-Zadeh, Maryam Chenaghloo, Amirhossein Jalali, Hassan Tatari, Maryam Aliramezany
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundTetralogy of Fallot is a common congenital heart disease characterized by cyanosis. The primary treatment approach involves corrective surgery typically performed within the first year of life to achieve complete resolution. However, certai
Externí odkaz:
https://doaj.org/article/18d97493244c4cf4afddfd2b0b87c0c7
Publikováno v:
Clinical Case Reports, Vol 11, Iss 9, Pp n/a-n/a (2023)
Key Clinical Message Although the combination of hypertrophic cardiomyopathy and slow flow coronary artery is a rare phenomenon, but a comprehensive evaluation of these patients is essential. Because timely diagnosis and treatment can prevent irrever
Externí odkaz:
https://doaj.org/article/f410f10d7c8d448d81f1c2ff8116593d
Publikováno v:
Journal of Emergency Practice and Trauma, Vol 8, Iss 2, Pp 152-155 (2022)
Objective: COVID-19 has now become a worldwide health problem with many new cases diagnosed every day. people with underlying heart diseases are more likely to get infected and have poor prognosis. Of them, adult patients with congenital heart diseas
Externí odkaz:
https://doaj.org/article/80fab5d04ca14da2bc565ae820a188c7
Autor:
Zahra Khajali, Maryam Aliramezany, Fateme Jorfi, Homa Ghaderian, Majid Maleki, Hadi Malek, Sara Lotfian, Yasaman Khalili, Nasim Naderi
Publikováno v:
JCSM Rapid Communications, Vol 5, Iss 1, Pp 77-85 (2022)
Abstract Background The chronic nature of congenital heart diseases (CHDs) leads to the activation of inflammatory and neurohormonal processes in the body, and there is a possibility of the occurrence of other complications such as sarcopenia. The ai
Externí odkaz:
https://doaj.org/article/99e93ea4f4c64c489d337eb36c63cda5
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2023)
IntroductionPrevalence of congenital heart disease (CHD) has increased in recent years, and patients with CHD have to deal with sequelae of the multiple medical and surgical treatments that can affect different aspects of their life which could be re
Externí odkaz:
https://doaj.org/article/526e49b3ca1d42d8a20acf1b78ce7906
Publikováno v:
Clinical Case Reports, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract Ebstein's anomaly is an uncommon congenital malformation which might be associated with atrial septal defect and atrio‐fascicular Mahaim. Here, we report a known case of Ebstein's anomaly with atrial septal defect and concomitant atrio‐f
Externí odkaz:
https://doaj.org/article/bff779e0beb74e2d821effa98982429d
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 12, Iss 3, Pp 237-243 (2020)
Hypoplastic right ventricle is a rare congenital disease usually associated with pulmonary atresia or tricuspid atresia. Isolated right ventricular hypoplasia is a rare anomaly without important valvular abnormalities. It is associated with inter atr
Externí odkaz:
https://doaj.org/article/062c137acf374887b58b4f5924c1173a
Publikováno v:
The Egyptian Heart Journal, Vol 72, Iss 1, Pp 1-5 (2020)
Abstract Background Aortic coarctation is currently treated by both surgical and transcatheter methods. Patients can present with late complication of prior surgical repair including recoarctation and aneurysm formation. There are limited reports on
Externí odkaz:
https://doaj.org/article/0762cf14546442d9a7d0f72f2c21c525