Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Fereshte Salami"'
Autor:
Marzieh Tavakol, Samaneh Delavari, Fereshte Salami, Sarina Ansari, Seyed Erfan Rasouli, Zahra Chavoshzadeh, Roya Sherkat, Hamid Ahanchian, Soheila Aleyasin, Hossein Esmaeilzadeh, Nasrin Moazzen, Alireza Shafiei, Farhad Abolnezhadian, Sara Iranparast, Sareh sadat Ebrahimi, Tannaz Moeini Shad, Salar Pashangzadeh, Farzad Nazari, Arezou Rezaei, Ali Saeedi-Boroujeni, Mohammad Nabavi, Saba Arshi, Morteza Fallahpour, Mohammad hassan Bemanian, Samin Sharafian, Sima Shokri, Sarvin Eshaghi, Shiva Nazari, Bibi Shahin Shamsian, Mehrdad Dargahi Mal-Amir, Roya Khazaei, Pooya Ashkevari, Armin Khavandegar, Sabahat Haghi, Marzie Esmaeili, Hassan Abolhassani, Nima Rezaei
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 18, Iss 1, Pp 1-9 (2022)
Abstract Genetic defects in the development, maturation, and/or function of the immune cells can lead to Inborn errors of immunity (IEI) which may predispose patients to malignancies. The overall risk for cancer in children with IEI ranges from 4 to
Externí odkaz:
https://doaj.org/article/78a7292b5c5c487085e67cfee390ff5b
Autor:
Gholamreza Azizi, Mina Fattah Hesari, Niusha Sharifinejad, Farimah Fayyaz, Zahra Chavoshzadeh, Seyed Alireza Mahdaviani, Mahnaz Seifi Alan, Mahnaz Jamee, Marzieh Tavakol, Homa Sadri, Ehsan Shahrestanaki, Mohammad Nabavi, Sareh Sadat Ebrahimi, Afshin Shirkani, Ahmad Vosughi Motlagh, Samaneh Delavari, Seyed Erfan Rasouli, Marzie Esmaeili, Fereshte Salami, Reza Yazdani, Nima Rezaei, Hassan Abolhassani
Publikováno v:
Journal of Clinical Immunology. 43:819-834
Purpose Primary B cell defects manifesting as predominantly antibody deficiencies result from variable inborn errors of the B cell lineage and their development, including impairments in early bone marrow development, class switch recombination (CSR)
Autor:
Nazanin Fathi, Hanieh Mojtahedi, Marzieh Nasiri, Hassan Abolhassani, Mahsa Yousefpour Marzbali, Marzie Esmaeili, Fereshte Salami, Furozan Biglari, Nima Rezaei
Publikováno v:
Expert Review of Clinical Immunology. 19:329-339
Autor:
Gholamreza Azizi, Fereshte Salami, Sahar Shariati, Seyed Erfan Rasouli, Samaneh Delavari, Marzieh Tavakol, Homa Sadri, Babak Asghari, Reza Yazdani, Nima Rezaei, Hassan Abolhassani
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 22:539-544
Background: Common variable immunodeficiency (CVID) is the most prevalent symptomatic primary immunodeficiencies. LPS-responsive beige-like anchor protein (LRBA) deficiency is a combined immunodeficiency characterized by a CVID-like phenotype. Affect
Autor:
Samaneh Delavari, Yating Wang, Tannaz Moeini shad, Salar Pashangzadeh, Farzad Nazari, Fereshte Salami, Hassan Abolhassani
Publikováno v:
Cancers
Volume 15
Issue 3
Pages: 764
Volume 15
Issue 3
Pages: 764
Inborn errors of immunity (IEI) are a heterogeneous group of inherited disorders, and almost 500 genes associated with these disorders have been identified. Defects in IEI genes lead to diverse clinical manifestations including increased susceptibili
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:
Samaneh Delavari, Lennart Hammarström, Sara Iranparast, Farhad Abolnezhadian, Nima Rezaei, Arezou Rezaei, Hamid Ahanchian, Minoo Mohraz, Meisam Sharifzadeh, Nasrin Moazzen, Sima Shokri, Saba Arshi, Tooba Momen, Ahmad Vosughimotlagh, Asghar Aghamohamamdi, Hassan Abolhassani, Mahnaz Sadeghi-Shabestari, Mohammad Nabavi, Tannaz Moeini Shad, Afshin Shirkani, Paniz Shirmast, Rasol Molatefi, Salar Pashangzadeh, Reza Yazdani, Mohammad Hassan Bemanian, Fereshte Salami, Morteza Fallahpour, Fateme Babaha, Molood Safarirad
Publikováno v:
Journal of Clinical Immunology
Although it is estimated that COVID-19 life-threatening conditions may be diagnosed in less than 1:1000 infected individuals below the age of 50, but the real impact of this pandemic on pediatric patients with different types of primary immunodeficie
Autor:
Asghar Aghamohammadi, Yasser Bagheri, Hassan Abolhassani, Seyed Alireza Mahdaviani, Mohammamd Nabavi, Afshin Shirkani, Reza Yazdani, Fereshte Salami, Gholamreza Azizi, Saba Fekrvand, Morteza Samadi, Sahar Shariati, Samaneh Delavari, Sepideh Shahkarami
Publikováno v:
Immunological Investigations. 51:381-394
Common variable immunodeficiency (CVID) is a primary immunodeficiency disease with a heterogeneous genetic background. Lipopolysaccharide-responsive beige-like anchor (LRBA), as well as cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), have impor
Autor:
Mohammad Shahrooei, Asghar Aghamohammadi, Reza Yazdani, Hassan Abolhassani, Afshin Shirkani, Fereshte Salami, Gholamreza Azizi
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 20:479-484
Background/Objective: LPS-responsive beige-like anchor protein (LRBA) deficiency is a combined immunodeficiency and immune dysregulation. The authors present a case report of LPSresponsive beige-like anchor protein (LRBA) deficiency with the history
Autor:
Hassan Abolhassani, Samaneh Delavari, Nils Landegren, Sima Shokri, Paul Bastard, Likun Du, Fanglei Zuo, Reza Hajebi, Farhad Abolnezhadian, Sara Iranparast, Mohammadreza Modaresi, Ahmad Vosughimotlagh, Fereshte Salami, Maribel Aranda-Guillén, Aurélie Cobat, Harold Marcotte, Shen-Ying Zhang, Qian Zhang, Nima Rezaei, Jean-Laurent Casanova, Olle Kämpe, Lennart Hammarström, Qiang Pan-Hammarström
Publikováno v:
The Journal of Allergy and Clinical Immunology
Background: Most severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-infected individuals are asymptomatic or only exhibit mild disease. In about 10% of cases, the infection leads to hypoxemic pneumonia, although it is much more rare in chil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5469fbdd4140fae65284bf82a345032d
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-493407
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-493407