Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Anahita Razaghian"'
Tumor Necrosis Factor-α (-308G>A) Gene Polymorphism and Its Association with Asthma and Atopy Status
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 22, Iss 4 (2023)
Asthma is one of the most prevalent chronic lung diseases that afflict genetically predisposed individuals. Certain cytokine gene polymorphisms have been associated with asthma. Tumor necrosis factor-alpha (TNF-α) is a potent inflammatory cytokine t
Externí odkaz:
https://doaj.org/article/5552599b0c604feaa3dcf178b56b5619
Autor:
Anahita Razaghian, Leila Parvaneh, Mona Delkhah, Arash Abbasi, Parisa Sadeghirad, Mohammad Shahrooei, Nima Parvaneh
Publikováno v:
eJHaem, Vol 1, Iss 1, Pp 334-337 (2020)
Abstract Hemophagocytic lymphohistiocytosis (HLH) disease is a severe immune dysregulation caused by mutations in genes required for lymphocyte cytotoxicity function. However, HLH‐like syndrome may develop secondary to infections, malignancy, and a
Externí odkaz:
https://doaj.org/article/1908685692904c609aae5d2213d4c384
Autor:
Yuta Ohishi, Sandra Ammann, Vahid Ziaee, Katharina Strege, Miriam Groß, Carla Vazquez Amos, Mohammad Shahrooei, Parisa Ashournia, Anahita Razaghian, Gillian M. Griffiths, Stephan Ehl, Mitsunori Fukuda, Nima Parvaneh
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Griscelli syndrome type 2 (GS-2) is an inborn error of immunity characterized by partial albinism and episodes of hemophagocytic lymphohistiocytosis (HLH). It is caused by RAB27A mutations that encode RAB27A, a member of the Rab GTPase family. RAB27A
Externí odkaz:
https://doaj.org/article/d08ade0fa09945848ee6988dbabd70b4
Publikováno v:
Iranian Journal of Neonatology, Vol 8, Iss 4, Pp 83-88 (2017)
Background: Neonatal hyperbilirubinemia is one of the most common causes of neonatal morbidity and a global health priority. This study aimed to evaluate the effect of intensive phototherapy on management of hyperbilirubinemia with different etiologi
Externí odkaz:
https://doaj.org/article/4b15e0d6ad724391b4af9a52234a8368
Autor:
Soheila Alyasin, Hamid Ahanchian, Babak Ghalebaghi, Sarehsadat Ebrahimi, Sima Shokri, Hassan Abolhassani, Nasrin Bazargan, Alireza Shafiei, Arash Kalantari, Mahnaz Sadeghi-Shabestari, Marzieh Heidarzadeh, Ramin Ghasemi, Mitra Tafakoridelbari, Javad Tafaroji, Javad Mohammadi, Marzieh Tavakol, Shiva Bayat, Afshin Shirkani, Arezou Rezaei, Taher Cheraghi, Mansoureh Shariat, Asghar Aghamohammadi, Nasrin Behniafard, Mohammad Hossein Eslamian, Azam Mohsenzadeh, Mehrnaz Mesdaghi, Fereshte Salami, Zahra Chavoshzadeh, Maryam Khoshkhui, Tannaz Moeini Shad, Reza Yazdani, Babak Negahdari, Samin Sharafian, Morteza Fallahpour, Behzad Shakerian, Samaneh Delavari, Roya Sherkat, Behzad Darabi, Anahita Razaghian, Setareh Mamishi, Mohammad Nabavi, Seyed Alireza Mahdaviani, Seyed Hesamedin Nabavizadeh, Sepideh Darougar, Akefeh Ahmadiafshar, Rasoul Nasiri Kalmarzi, Mojgan Moghtaderi, Nima Rezaei, Farahzad Jabbari-Azad, Seyed Erfan Rasouli, Hossein Ali Khazaei, Salar Pashangzadeh, Gholamreza Hassanpour, Javad Ghaffari, Abbas Khalili, Hossein Esmaeilzadeh, Gholamreza Azizi, Rasol Molatefi, Seyed Mohammad Fathi, Paniz Shirmast, Mahnaz Jamee, Parisa Ashournia, Mohammad Hassan Bemanian, Ahmad Vosughimotlagh, Hamid Eshaghi, Maziyar Rahimi Haji-Abadi, Saeed Bazregari, Abbas Dabbaghzadeh, Saba Arshi, Tooba Momen
Publikováno v:
Pediatric Allergy and Immunology. 32:1335-1348
BACKGROUND: The inborn errors of immunity (IEIs) are a group of heterogeneous disorders mainly characterized by severe and recurrent infections besides other complications including autoimmune and inflammatory diseases. In this study, we aim to evalu
Autor:
Mona Delkhah, Leila Parvaneh, Parisa Sadeghirad, Mohammad Shahrooei, Arash Abbasi, Nima Parvaneh, Anahita Razaghian
Publikováno v:
eJHaem. 1:334-337
Autor:
Paniz Shirmast, Seyed Mohammad Fathi, Mahnaz Jamee, Shiva Bayat, Maryam Khoshkhui, Mohammad Hassan Bemanian, Rasol Molatefi, Javad Ghaffari, Arezou Rezaei, Arash Kalantari, Samin Sharafian, Behzad Shakerian, Samaneh Delavari, Ramin Ghasemi, Mohammad Hossein Eslamian, Parisa Ashournia, Mehrnaz Mesdaghi, A.R. Shafiei, Morteza Fallahpour, Behzad Darabi, Hassan Abolhassani, Marzieh Heidarzadeh, Mahnaz Sadeghi-Shabestari, Hamid Ahanchian, Gholamreza Azizi, Javad Mohammadi, Taher Cheraghi, Azam Mohsenzadeh, Ahmad Vosughimotlagh, Nima Rezaei, Fereshte Salami, Zahra Chavoshzadeh, Roya Sherkat, Sarehsadat Ebrahimi, Tannaz Moeini Shad, Abbas Khalili, Babak Negahdari, Setareh Mamishi, Nasrin Bazargan, Sepideh Darougar, Akefeh Ahmadiafshar, Seyed Alireza Mahdaviani, Gholamreza Hassanpour, Afshin Shirkani, Reza Yazdani, Anahita Razaghian, Mansoureh Shariat, Soheila Alyasin, Farahzad Jabbari-Azad, Mohammad Nabavi, Salar Pashangzadeh, Rasoul Nasiri Kalmarzi, Marzieh Tavakol, Saba Arshi, Tooba Momen, Hamid Eshaghi, Maziyar Rahimi Haji-Abadi, Saeed Bazregari, Abbas Dabbaghzadeh, Hossein Esmaeilzadeh, Mojgan Moghtaderi, Sima Shokri, Mitra Tafakoridelbari, Javad Tafaroji, Seyed Hesamedin Nabavizadeh, Babak Ghalebaghi, Nasrin Behniafard, Seyed Erfan Rasouli, Hossein Ali Khazaei, Asghar Aghamohammadi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77bf2c6aa053c3884f985449509cd7bd
https://doi.org/10.1111/pai.13510/v2/response1
https://doi.org/10.1111/pai.13510/v2/response1
Autor:
Marziyeh Tavakol, Soheila Alyasin, Gholamreza Hassanpour, Afshin Shirkani, Arezou Rezaei, Mansoureh Shariat, Mohammad Hassan Bemanian, Asghar Aghamohammadi, Anahita Razaghian, Mahsa Sohani, Samin Sharafian, Behzad Darabi, Salar Pashangzadeh, Setareh Mamishi, Mitra Tafakoridelbari, Javad Tafaroji, Fateme Babaha, Sepideh Darougar, Akefeh Ahmadiafshar, Hamid Ahanchian, Hossein Esmaeilzadeh, Parisa Ashournia, Reza Yazdani, Mojgan Moghtaderi, Abbas Khalili, Babak Ghalebaghi, Rasoul Nasiri Kalmarzi, Morteza Fallahpour, Seyed Erfan Rasouli, Mohammad Hossein Asgardoon, Saba Arshi, Roya Sherkat, Hassan Abolhassani, Hossein Ali Khazaei, Sarehsadat Ebrahimi, Tooba Momen, Arash Kalantari, Mohammad Hossein Eslamian, Maryam Khoshkhui, Mehrnaz Mesdaghi, Mahnaz Sadeghi-Shabestari, Babak Negahdari, Nima Rezaei, Javad Mohammadi, Seyed Alireza Mahdaviani, Fereshte Salami, Javad Ghaffari, Azam Mohsenzadeh, Farahzad Jabbari-Azad, Ashraf Samavat, Zahra Chavoshzadeh, Paniz Shirmast, Behzad Shakerian, Samaneh Delavari, Alireza Shafiei, Ahmad Vosughimotlagh, Nasrin Behniafard, Mahnaz Jamee, Marzieh Heidarzadeh, Maziyar Rahimi Haji-Abadi, Taher Cheraghi, Rasol Molatefi, Abbas Dabbaghzadeh, Mohammad Nabavi, Gholamreza Azizi, Seyed Mohammad Fathi
Publikováno v:
International archives of allergy and immunology. 181(9)
Background: Common variable immunodeficiency (CVID) is the most frequent primary immunodeficiency disorder mainly characterized by recurrent bacterial infections besides other immunological defects including loss of or dysfunction of B cells and decr
Autor:
Maziar Rahimi Hajiabadi, Roja Rouhani, Nima Rezaei, Peter Olbrich, A.R. Shafiei, Hassan Abolhassani, Mansoureh Shariat, Mohammadreza Modaresi, Zahra Shahraki‐Ghadimi, Fatemeh Hoda Fallah, Mahsa Sohani, Reza Yazdani, Rohola Shirzadi, Samaneh Delavari, Gholamreza Hassanpour, Arash Kalantari, Gholamreza Azizi, Parisa Ashournia, Saba Fekrvand, Na Lu, Marzieh Asgharyan, Anahita Razaghian, Asghar Aghamohammadi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e3fb5defea5e28ebf9da97c1625780a
https://doi.org/10.1111/pai.13228/v2/response1
https://doi.org/10.1111/pai.13228/v2/response1
Autor:
Anahita Razaghian, Peter Olbrich, Mohammadreza Modaresi, Mansoureh Shariat, Gholamreza Azizi, Parisa Ashournia, Alireza Shafiei, Arash Kalantari, Saba Fekrvand, Nima Rezaei, Fatemeh Hoda Fallah, Gholamreza Hassanpour, Hassan Abolhassani, Asghar Aghamohammadi, Mahsa Sohani, Na Lu, Maziar Rahimi Hajiabadi, Reza Yazdani, Marzieh Asgharyan, Zahra Shahraki‐Ghadimi, Rohola Shirzadi, Samaneh Delavari, Roja Rouhani
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
Universitat Politècnica de Catalunya (UPC)
Universitat Politècnica de Catalunya (UPC)
[Background] Congenital agammaglobulinemia is the first primary immunodeficiency disorder characterized by a defect in B lymphocyte development and subsequently decreased immunoglobulin levels. These patients are prone to suffer from recurrent infect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b28cfe8f655b2e95fa01d172badcff3
http://hdl.handle.net/10261/236383
http://hdl.handle.net/10261/236383