Search Results - "Boloursaz, Mohammadreza"

Whole lung lavage of nine children with pulmonary alveolar proteinosis: experience in a tertiary lung center by Badiozaman, Radpay, Tahereh, Parsa, Shideh, Dabir, Mohammadreza, Boloursaz, Ahmadreza, Arbab, Seyyedahmad, Tabatabaei

“…Pulmonary alveolar proteinosis (PAP) is a rare disease in children, characterized by intra-alveolar accumulation of large amounts of surfactant proteins, which…”
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Association Between Prevalence of Depression and Anxiety in Cystic Fibrosis Patients and Their Parents: A Cross-sectional Study in Iran by Orooji, Azam, Valinejadi, Ali, Hassanzad, Maryam, Boloursaz, Mohammadreza, Velayati, Ali Akbar

“…Background: Patients with chronic diseases and their caregivers are at risk for mental disorders, such as depression and anxiety. Objectives: This study aimed…”
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Evaluation of miR-155 Expression in Cystic Fibrosis Patients by Yasseri, Somayeh, Hassanzad, Maryam, Farnia, Poopak, Ghanavi, Jalaledin, Boloursaz, Mohammadreza, Velayati, Ali Akbar

“…Background: Cystic Fibrosis (CF) is the most fatal genetic disorder among white populations. It is a multi-system disease with various symptoms, which causes…”
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Evaluation of Quality of Life in Patients with Cystic Fibrosis Regarding Smoking History in Parents by Eslampanah, Shabnam, Hassanzad, Maryam, Valinejadi, Ali, Ghaffaripoor, Hossein Ali, Boloursaz, Mohammadreza, Mahdaviani, Seyed Alireza, Baghaei, Noushin, Daneshmandi, Zahra, Mohammadpour, Leila, Velayati, Ali Akbar

“…Background: The provision of facilities to achieve better living conditions for patients with cystic fibrosis (CF) is of particular importance. Smoking is one…”
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Pulmonary Alveolar Proteinosis in Children: Diagnosis and Treatment Outcomes by Hassanzad, Maryam, Tashayoie-Nejad, Sabereh, Boloursaz, Mohammadreza, Mahdaviani, Seyed Alireza, Baghaie, Nooshin, Ghaffaripour, Hosseinali, Aghahosseini, Farahnaz, Hossein Ahmadi, Zargham, Parsa, Tahereh, Farzanegan, Behrooz, Fakharian, Atefeh, Seyedi, Seyed Javad, Velayati, Ali Akbar

“…BackgroundPulmonary Alveolar Proteinosis (PAP) is an uncommon pulmonary disease characterized by the accumulation of surfactant composed of proteins and lipids…”
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Pulmonary complications of predominantly antibody immunodeficiencies in a tertiary lung center by Mahdaviani, Seyed Alireza, Darougar, Sepideh, Mansouri, Davood, Tashayoie-Nejad, Sabereh, Movahedi, Mahshid, Aghdam, Karim Rahimi, Ghaffaripour, Hosseinali, Baghaie, Nooshin, Hassanzad, Maryam, Eslaminejad, Alireza, Fakharian, Atefeh, Pourdowlat, Guitti, Heshmatnia, Jalal, Bakhshayeshkaram, Mehrdad, Boloursaz, Mohammadreza, Tabarsi, Payam, Hashemitari, Seyed Karen, Velayati, Ali Akbar

“…Respiratory infections are expressed very soon in the life in humoral immunodeficiencies and often lead to chronic irreversible complications such as…”
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Surgical and Medical Treatments of Empyema in Pediatric Patients by Hassanzad, Maryam, Khalilzadeh, Soheila, Boloursaz, Mohammadreza, Riazi Kermany, Khadijeh, Baghaie, Nooshin, Tashayoie Nejad, Sabereh, Mohajerani, Seyed Amir, Saghebi, Seyed Reza, Mehrian, Payam, Velayati, Ali Akbar

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Whole lung lavage of nine children with pulmonary alveolar proteinosis: experience in a tertiary lung center by Badiozaman, Radpay, Tahereh, Parsa, Shideh, Dabir, Mohammadreza, Boloursaz, Ahmadreza, Arbab, Seyyedahmad, Tabatabaei

“…BACKGROUNDPulmonary alveolar proteinosis (PAP) is a rare disease in children, characterized by intra-alveolar accumulation of large amounts of surfactant…”
Get full text