Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Maziar Gholampour dehaki"'
Autor:
Zahra Amirsardari, Fatemeh Amirsardari, Erfan Kohansal, Amir Ghaffari Jolfay, Maziar Gholampour Dehaki, Vahid Ziaee
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-8 (2024)
Abstract Background Kawasaki Disease (KD) involves arterial inflammation, primarily affecting the coronary arteries and leading to coronary artery lesions. Recent advancements in understanding the immunomodulatory roles of vitamin D have prompted inv
Externí odkaz:
https://doaj.org/article/749ae1eef74e49e3a6968c24e9d9ea33
Autor:
Mohammad Mahdavi, Golnar Mortaz Hejri, Hossein Shahzadi, Maziar Gholampour Dehaki, Golnaz Houshmand
Publikováno v:
ESC Heart Failure, Vol 10, Iss 4, Pp 2630-2636 (2023)
Abstract Aims Transplant services were imposed to the multiple challenges of insufficient facilities and resources during the COVID‐19 pandemic. Thus, each centre modified and altered its routine practice to maintain the service. We report our expe
Externí odkaz:
https://doaj.org/article/f0bd492897f14b2c9ece3c655d2fb0ab
Autor:
Shiva Khaleghparast, Majid Maleki, Ghasem Hajianfar, Esmaeil Soumari, Mehrdad Oveisi, Hassan Maleki Golandouz, Feridoun Noohi, Maziar Gholampour dehaki, Reza Golpira, Saeideh Mazloomzadeh, Maedeh Arabian, Samira Kalayinia
Publikováno v:
BMC Health Services Research, Vol 23, Iss 1, Pp 1-12 (2023)
Abstract Background Patients’ rights are integral to medical ethics. This study aimed to perform sentiment analysis and opinion mining on patients’ messages by a combination of lexicon-based and machine learning methods to identify positive or ne
Externí odkaz:
https://doaj.org/article/7ae8a87605cc4c99bdc49d9b83d81a7b
Autor:
Hassan Tatari, Gholamreza Omrani, Maedeh Arabian, Kambiz Mozaffari, Yaser Toloueitabar, Sanaz Asadian, Nader Givtaj, Maziar Gholampour Dehaki, Amirhosein Jalali
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 14, Iss 1, Pp 47-52 (2022)
Introduction: The autologous pericardium, treated or fresh, is used in reconstructive cardiovascular surgery. We aimed to describe the features of fresh pericardium utilized in right ventricular outflow tract (RVOT) reconstruction, years after the in
Externí odkaz:
https://doaj.org/article/88c64e1948b74b02a466e55336f966c3
Autor:
Anita Sadeghpour, MD, Nakisa Khansari, MD, Marziyeh Pakbaz, MD, Kiara Rezaei Kalantari, MD, Hamidreza Pouraliakbar, MD, Maziar Gholampour Dehaki, MD
Publikováno v:
JACC: Case Reports, Vol 1, Iss 4, Pp 540-544 (2019)
Double aortic arch, the most common vascular ring, causes a complete ring surrounding the esophagus and trachea that leads to compressive symptoms. This report describes a young woman with a history of totally corrected tetralogy of Fallot who was a
Externí odkaz:
https://doaj.org/article/497f60246551488e8f13f176b984c2f5
Autor:
Maziar Gholampour dehaki, Rasol Azarfarin, Hooman Bakhshande Abkenar, Mohammad Mahdavi, Azin Aliazdehasl, Sana Niknam, Azadeh Niknam
Publikováno v:
مراقبت پرستاری و مامایی ابن سینا, Vol 27, Iss 2, Pp 107-115 (2019)
Introduction: Pediatric Cardiopulmonary Bypass (CPB) circuit invariably requires priming with Packed Red Blood Cells (PRBCs). Metabolic composition of stored PRBCs is unphysiological. Commencement of PRBC primed CPB leads to rapid transfusion of mass
Externí odkaz:
https://doaj.org/article/80be3f0c86d14be3b9aef27d38b276aa
Autor:
Mohammad Mahdavi, Golnar Morataz Hejri, Hooman Bakhshandeh, Ahmad Amin, Ali Sadeghpour Tabaei, Maziar Gholampour Dehaki, Saeid Hosseini, Zeai Totonchi, Bahador Baharestani
Publikováno v:
Research in Cardiovascular Medicine, Vol 7, Iss 1, Pp 31-34 (2018)
Introduction: Heart transplantation is the ultimate treatment method for many infants and children with the diagnosis of cardiomyopathy or final stages of congenital heart failure. Purpose: This report provides the results of children's heart transpl
Externí odkaz:
https://doaj.org/article/964f5013d2db485190fdc1bee8067b31
Autor:
Alwaleed Al-Dairy, Yousef Rezaei, Maziar Gholampour Dehaki, Anita Sadeghpour, Zia Totonchi, Hamidreza Pouraliakbar, Alireza Alizadeh Ghavidel
Publikováno v:
Iranian Journal of Medical Sciences, Vol 42, Iss 6, Pp 599-602 (2017)
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiac malformation. We report three cases of ALCAPA who survived to adulthood. The first case was a 51-year-old woman who complained of typical che
Externí odkaz:
https://doaj.org/article/ac91c9bcfa274c10b6995edd529b35bb
Autor:
Maziar Gholampour Dehaki, Alwaleed Al-Dairy, Yousef Rezaei, Alireza Alizadeh Ghavidel, Gholamreza Omrani, Nader Givtaj, Reza Sadat Afjehi, Hassan Tatari, Amir Hossein Jalali, Mohammad Mahdavi
Publikováno v:
Annals of Pediatric Cardiology, Vol 10, Iss 2, Pp 137-143 (2017)
Background: Anomalous origin of left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital malformation. We sought to evaluate in-hospital and mid-term outcomes of patients with a diagnosis of ALCAPA who underwent surgical repair. O
Externí odkaz:
https://doaj.org/article/8f1a2c990adb4f248a56eee5b0b76d4b
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 6, Iss 2, Pp 91-95 (2014)
Introduction: Excessive bleeding presents a risk for the patient in cardiovascular surgery. Local haemostatic agents are of great value to reduce bleeding and related complications. TachoSil (Nycomed, Linz, Austria) is a sterile, haemostatic agent th
Externí odkaz:
https://doaj.org/article/904dc20660814f179c810fd9ae575409