Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Nooshin, Baghaie"'
Autor:
Mahsa Eskian, Payam Tabarsi, Mahshid Movahedi, Mehrnaz Mesdaghi, Mihan Poorabdolah, Abdollah Karimi, Parisa Farnia, Davood Mansouri, Majid Zaki-Dizaji, Mehdi Ghaini, Jean-Laurent Casanova, Ali Akbar Velayati, Majid Marjani, Zahra Chavoshzadeh, MirHojjat Khorasanizadeh, Nima Rezaei, Jacinta Bustamante, Hosseinali Ghaffaripour, Shabnam Eskandarzadeh, Seyed Alireza Mahdaviani, Maryam Hassanzad, Karim Rahimi Aghdam, Nooshin Baghaie, Farzad Noori, Shahram Kahkooi, Mahnaz Jamee, Stéphanie Boisson-Dupuis, Mahboubeh Mansouri, Esmail Mortaz, Afshin Moniri
Publikováno v:
Journal of Clinical Immunology. 40:872-882
Mendelian susceptibility to mycobacterial diseases (MSMD) is a rare congenital condition characterized by a selective predisposition to infections caused by weakly virulent mycobacteria and other types of intra-macrophagic pathogens. The 16 genes ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e104f0e204bb5c9db69a23319cd7dc6a
https://doi.org/10.1007/s10875-020-00813-7
https://doi.org/10.1007/s10875-020-00813-7
Autor:
Soheila Khalilzadeh, Shahram Kahkouee, Maryam Hassanzad, Nazanin Parsanejad, Nooshin Baghaie, Mohammad Reza Bloorsaz
Publikováno v:
Iranian Journal of Medical Sciences, Vol 36, Iss 1, Pp 18-23 (2011)
Background: To reduce the mortality and morbidity rates of cystic fibrosis (CF) patients, and to have an effective clinical management, it is important to monitor the progression of the disease. The aim of this study was to evaluate the progression o
Externí odkaz:
https://doaj.org/article/c5a6c8dbc24147a1a1b46f8f80f68b5f
Autor:
Nooshin Baghaie, Soheila Khalilzade, Mohammad Reza Boloursaz, Amir Ali Khodayari, Ali Akbar Velayati
Publikováno v:
Acta Medica Iranica, Vol Vol. 48, Iss No. 4, Pp 239-243 (2010)
"nTuberculosis (TB) is an important health problem in developing countries, with varying clinical presentations depending on the organs/systems involved. To study the spectrum of clinical and paraclinical aspects of extra pulmonary TB in children suf
Externí odkaz:
https://doaj.org/article/cd6af06c92084a5b84e36d8b742f98e9
Autor:
Mohmmad Reza Boloursaz, Soheila Khalilzadeh, Nooshin Baghaie, Amir Ali Khodayari, Ali Akbar Velayati
Publikováno v:
Acta Medica Iranica, Vol Vol. 48, Iss No. 4, Pp 244-249 (2010)
"nDespite the extensive preventive and therapeutic measures present against tuberculosis (TB), this disease still remains as one of the important causes of mortality and morbidity in the world. Considering the high incidence of TB in children, rarene
Externí odkaz:
https://doaj.org/article/3c0b723985ea44a1b8713544c131730a
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc185db63f2a51290ec04579d9cb6b0d
http://europepmc.org/articles/PMC7044568
http://europepmc.org/articles/PMC7044568
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af723bd4facc1dd195edd6260b073274
https://pubmed.ncbi.nlm.nih.gov/36267924
https://pubmed.ncbi.nlm.nih.gov/36267924
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6355f8891baa810f22d96574a3bdb201
http://europepmc.org/articles/PMC7044566
http://europepmc.org/articles/PMC7044566
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f33d495aeb8a11389df3e3a8169c83c
https://pubmed.ncbi.nlm.nih.gov/28009030
https://pubmed.ncbi.nlm.nih.gov/28009030
Autor:
Mohammad Reza Boloursaz, Nazanin Parsanejad, Soheila Khalilzadeh, Nooshin Baghaie, Fanak Fahimi, Maryam Hassanzad
Publikováno v:
Journal of Comprehensive Pediatrics. 4:82-5
Background: Cystic fibrosis is a complex progressive disease which assessing its progression and severity is essential. For this purpose there are scoring systems available to evaluate the disease severity. Objectives: The aim of the present study wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e720d59412cadd1b3e0eae6d04c95c
https://doi.org/10.17795/compreped-4558
https://doi.org/10.17795/compreped-4558
Autor:
Maryam Hassanzad, Soheila Khalilzadeh, Habib Emami, Mohamad Reza Boloursaz, Elaheh Heydarian Fard, Nooshin Baghaie
Publikováno v:
Journal of Comprehensive Pediatrics. 3:25-28
Article type: Original Article Background: Cystic fibrosis (CF) is a genetic disease with an autosomal recessive pattern of inheritance. CF caused by a mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::170632742acd053ec1c3a2dd3fa4bcba
https://doi.org/10.17795/compreped-6944
https://doi.org/10.17795/compreped-6944