Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sabereh Tashayoie Nejad"'
Autor:
Maryam Hassanzad, Soheila Khalilzadeh, Shabnam Eslampanah Nobari, Mohammadreza Bloursaz, Hooman Sharifi, Seyed Amir Mohajerani, Sabereh Tashayoie Nejad, Ali Akbar Velayati
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 14, Iss 1 (2015)
Asthma environmental triggers play important roles in severity of disease. Passive smoking could exacerbate asthma symptoms and enhance the decrease in lung function. Cotinine levels could be a reflection of passive exposure to the cigarette both in
Externí odkaz:
https://doaj.org/article/b60197c8e3814f1298d62b34969579a1
Autor:
Hassan Mozaffari Khosravi, Mohammad Ali Hojjati Kermani, Maryam Hassanzad, Mansour Rezaie, Sabereh Tashayoie-Nejad, Seyed Javad Sayedi, Ali Akbar Velayati
Publikováno v:
International Journal of Pediatrics, Vol 7, Iss 4, Pp 9285-9294 (2019)
Background: Cystic Fibrosis (CF) is a hereditary autosomal recessive genetic disorder that can affect many organs including the lungs and the digestive system. We aimed to assess the effects of coenzyme Q10 level on clinical parameters in cystic fibr
Autor:
Karim Rahimi Aghdam, Maryam Hassanzad, M R Boloursaz, Mehrdad Bakhshayeshkaram, Sabereh Tashayoie-Nejad, Ali Akbar Velayati, Hosseinali Ghaffaripour, Guitti Pourdowlat, Seyed Karen Hashemitari, Nooshin Baghaie, Davood Mansouri, Jalal Heshmatnia, Seyed Alireza Mahdaviani, Alireza Eslaminejad, Atefeh Fakharian, Payam Tabarsi, Mahshid Movahedi, Sepideh Darougar
Publikováno v:
Interventional Medicine & Applied Science
Background and aims Respiratory infections are expressed very soon in the life in humoral immunodeficiencies and often lead to chronic irreversible complications such as bronchiectasis and chronic airflow limitation. This study was conducted to evalu
Autor:
Maryam, Hassanzad, Sabereh, Tashayoie-Nejad, Mohammadreza, Boloursaz, Seyed Alireza, Mahdaviani, Nooshin, Baghaie, Hosseinali, Ghaffaripour, Farahnaz, Aghahosseini, Zargham, Hossein Ahmadi, Tahereh, Parsa, Behrooz, Farzanegan, Atefeh, Fakharian, Seyed Javad, Seyedi, Ali Akbar, Velayati
Publikováno v:
Tanaffos. 20(4)
Pulmonary Alveolar Proteinosis (PAP) is an uncommon pulmonary disease characterized by the accumulation of surfactant composed of proteins and lipids due to disruption of surfactant clearance by alveolar macrophages. The current standard treatment is
Autor:
Nooshin Baghaie, Sepideh Darougar, Seyed Alireza Nadji, Sabereh Tashayoie-Nejad, Maryam Hassanzad, Seyed Alireza Mahdaviani, Ali Akbar Velayati, Hosseinali Ghaffaripour, Mohammad Reza Boloursaz
Publikováno v:
Interventional Medicine & Applied Science
Interventional Medicine and Applied Science
Interventional Medicine and Applied Science
Introduction Asthma exacerbations may occur due to a variety of triggers including respiratory viruses. The aim of this study was to determine the role of particular viral infections in asthma exacerbations in children. Materials and methods The stud
Autor:
Sabereh Tashayoie Nejad, Maryam Hassanzad, Farzaneh Salem, Amir Ali Mahboobipour, Shadi Baniasadi
Publikováno v:
Drug metabolism and personalized therapy. 35(1)
Background Hospitalized pediatric patients are at an increased risk of experiencing potential drug-drug interactions (pDDIs) due to polypharmacy and the unlicensed and off-label administration of drugs. The aim of this study is to characterize clinic
Autor:
Soheila, Khalilzadeh, Maryam, Hassanzad, Mihan, PourAbdollah Toutkaboni, Sabereh, Tashayoie Nejad, Fatemeh-Maryam, Sheikholeslami, Ali Akbar, Velayati
Publikováno v:
Tanaffos
Background: Cystic Fibrosis (CF) is a life-threatening recessive genetic disorder resulting from mutations in the gene encoding the fibrosis transmembrane conductance regulator protein (CFTR). The CF clinical phenotype shows wide variation ranging fr
Publikováno v:
Paediatric Bronchology.
Autor:
Maryam Hassanzad, Ali Akbar Velayati, Sabereh Tashayoie Nejad, Shahram Kharabian Masouleh, Saba Karimzadeh
Publikováno v:
Iranian Journal of Pediatrics. 27
Background: Respiratory failure secondary to recurrent respiratory infections is the most common cause of death in Cystic fibrosis (CF). Objectives: To assess the efficacy of noninvasive positive pressure ventilation (NIPPV) on respiratory function,
Autor:
Sepideh Darougar, Sabereh Tashayoie Nejad, Seyed Karen Hashemitari, Seyed Amir Mohajerani, Nooshin Baghaie, Mohammad Reza Boloursaz, Ali Akbar Velayati, Maryam Hassanzad
Publikováno v:
Advances in Respiratory Medicine; Volume 84; Issue 6; Pages: 310-315
Introduction: Cystic fibrosis is a chronic disease with multiple organ involvement and chiefly results in chronic respiratory infections, pancreatic insufficiency and associated complications. The age at diagnosis, clinical presentation, rate of dise