Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Freidoon Noohi"'
Autor:
Azin Alizadehasl, Arezoo Mohamadifar, Bahram Mohebbi, Mohsen Ziyaeifard, Freidoon Noohi Bezanjani, Solmaz Valizadeh, Fatemeh Zohrian, Rasoul Azarfarin, Seifolah Abdi
Publikováno v:
Multidisciplinary Cardiovascular Annals. 11
Central venous access is commonly performed in the care of critically ill patients, for administration of repeated drug treatments. This routine procedure has multiple complications such as catheter malposition, migration, obstruction, infection, thr
Autor:
Mohammad Javad Alamzadeh Ansari, Azin Alizadehasl, Leili Poorafkari, Alireza Alizadeh Ghavidel, Behshid Ghadrdoost, Freidoon Noohi Bezanjani, Rashideh Siami
Publikováno v:
Multidisciplinary Cardiovascular Annals. 10
Introduction: Kawasaki disease (KD) is a systemic vasculitis syndrome usually presented with acute fever which occurs primarily in children younger than 5 years of age. KD has become the most common cause of acquired heart disease in pediatric popula
Autor:
Azin Alizadehasl, Samaneh Pourhosseinali, Freidoon Noohi, Raheleh Kaviani, Mohammad Mehdi Peighambari, Alireza Alizadeh Ghavidel, Rasoul Azarfarin, Majid Kyavar
Publikováno v:
Multidisciplinary Cardiovascular Annals.
Introduction: The left atrial appendage (LAA) lies within the confines of the pericardium in close relation to the free wall of the left ventricle. The LAA is long and thin with a narrow base. The LAA is best evaluated by transesophageal echocardiogr
Autor:
Akram Zamani, Nafiseh Kuchekian, Maryam Montazeri, Freidoon Noohi, Massoud Houshmand, Givtaj Nozar
Publikováno v:
Archives of Medical Science : AMS
Introduction mtDNA defects, both deletions and point mutations, have been associated with hypertrophic cardiomyopathies. The aim of this study was to establish a spectrum for mtDNA mutations in Iranian hypertrophic cardiomyopathy (HCM) patients. Mate