Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mahsa Sohani"'
Autor:
Mehdi Bakhtiyaridovvombaygi, Somayeh Yazdanparast, Setare Kheyrandish, Seyed Mehrab Safdari, Fateme Amiri Samani, Mahsa Sohani, Akram Sadat Jaafarian, Fateme Damirchiloo, Amirhossein Izadpanah, Sahar Parkhideh, Fatemeh Mikanik, Elham Roshandel, Abbas Hajifathali, Ahmad Gharehbaghian
Publikováno v:
Biomarker Research, Vol 12, Iss 1, Pp 1-44 (2024)
Abstract Non-Hodgkin lymphomas (NHLs) are heterogeneous and are among the most common hematological malignancies worldwide. Despite the advances in the treatment of patients with NHLs, relapse or resistance to treatment is anticipated in several pati
Externí odkaz:
https://doaj.org/article/3a0a338346264057a589263ac2d40f6e
Publikováno v:
Cell Journal, Vol 24, Iss 12, Pp 757-763 (2022)
Objective Chronic myeloid leukemia (CML) is a myeloproliferative malignancy with different stages. Aberrant epigeneticmodifications, such as DNA methylation, have been introduced as a signature for diverse cancers which also plays acrucial role in CM
Externí odkaz:
https://doaj.org/article/45489a85c3334a6f89089f5d4432642d
Autor:
Mahsa Sohani, Shahrbano Rostami, Mehdi Azad, Tahereh Hojjatipour, Bahram Chahardouli, Shaban Alizadeh
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 15, Iss 1 (2021)
Background: Although the precise pathogenesis of acute lymphoblastic leukemia (ALL) remains unclear, studying gene-regulating mechanisms during ALL pathogeneses may shed light on the underlying mechanisms driving malignant behavior. There is some evi
Externí odkaz:
https://doaj.org/article/3a8666dd0c5e4bb78bfe08375d2060cb
Autor:
Marzieh Tavakol, Waleed Al-Herz, Gholamreza Azizi, Arash Kalantari, Asghar Aghamohammadi, Vicki Modell, Ahmed Aziz Bousfiha, Fred Modell, Monireh Mohsenzadegan, Lennart Hammarström, Hossein Esmaeilzadeh, Hassan Abolhassani, Tooba Momen, Mahnaz Sadeghi-Shabestari, Samaneh Delavari, Laleh Sharifi, Reza Yazdani, Antonio Condino-Neto, Mahsa Sohani, Jessica Quinn, Soheila Aleyasin, Mikko Seppänen, Jordan S. Orange, Zahra Chavoshzadeh, Paniz Shirmast, Roya Sherkat, Kathleen E. Sullivan, Hamid Ahanchian, Farahzad Jabbari-Azad, Seyed Alireza Mahdaviani
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
During the last 4 decades, registration of patients with primary immunodeficiencies (PID) has played an essential role in different aspects of these diseases worldwide including epidemiological indexes, policymaking, quality controls of care/life, fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aee76e520c29033d23373fe1e5881edb
https://doi.org/10.1080/1744666x.2020.1801422
https://doi.org/10.1080/1744666x.2020.1801422
Autor:
Farzad Nazari, Asghar Aghamohammadi, Sohail Mozdarani, Yasser Bagheri, Hassan Abolhassani, Saba Fekrvand, Mahsa Sohani, Gholamreza Hassanpour, Fatemeh Kiaee, Gholamreza Azizi, Hossein Mozdarani, Samaneh Delavari, Reza Yazdani
Publikováno v:
Immunological Investigations. 50:580-596
HIGM syndrome is a rare form of primary immunodeficiencies characterized by normal/increased amounts of serum IgM and decreased serum levels of other switched immunoglobulin classes. Since the affected patients are continuously infected with various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eabb6e6c16be1cf6c760161283a2f21
https://doi.org/10.1080/08820139.2020.1779288
https://doi.org/10.1080/08820139.2020.1779288
Autor:
Mohammadreza Modaresi, Bobak Moazzami, Asghar Aghamohammadi, Rohola Shirzadi, Fatemeh Kiaei, Gholamreza Azizi, Mahsa Sohani, Seyed Alireza Mahdaviani, Reza Yazdani, Hassan Abolhassani, Mitra Tafakori
Publikováno v:
Journal of Clinical Immunology. 39:557-568
Hyper Immunoglobulin M (HIgM) syndrome is a heterogeneous group of primary immunodeficiency disorders, characterized by recurrent infections and associated with decreased serum IgG and IgA, but normal or increased IgM. The aim of the present study wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b305020ae781014f386f9a0b66842af
https://doi.org/10.1007/s10875-019-00650-3
https://doi.org/10.1007/s10875-019-00650-3
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bbcffee0b48795999056c5b61fb0a4c
https://pubmed.ncbi.nlm.nih.gov/32615565
https://pubmed.ncbi.nlm.nih.gov/32615565
Autor:
Hassan Abolhassani, Asghar Aghamohammadi, Tannaz Moeini Shad, Samaneh Delavari, Seyed Mohammad Akrami, Gholamreza Hassanpour, Sepideh Shahkarami, Fatemeh Kiaei, Mahsa Sohani, Parisa Amirifar, Arezou Rezaei, Reza Yazdani, Hossein Mozdarani
Publikováno v:
Immunological investigations. 50(2-3)
Objectives: Ataxia-telangiectasia (A-T) is an autosomal recessive neurodegenerative disorder with multisystem involvement caused by homozygous or compound heterozygous mutations in the ataxia telan...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43001747b0b5d1664bba167dc0d5b4c7
https://pubmed.ncbi.nlm.nih.gov/32116070
https://pubmed.ncbi.nlm.nih.gov/32116070
Autor:
Abubakar Umar Anka, Setareh Mamishi, Reza Yazdani, Gholamreza Azizi, Arash Kalantari, Asghar Aghamohammadi, Sepideh Shahkarami, Paniz Shirmast, Hassan Abolhassani, Alireza Shafiei, Mahsa Sohani, Sima Habibi, Mansoureh Shariat, Samaneh Delavari, T. Moeini Shad, Farzad Nazari, Gholamreza Hassanpour
Publikováno v:
Allergologia et immunopathologia. 48(6)
Background Bacille Calmette-Guerin (BCG) vaccination has a great impact on the prevention of severe complications of tuberculosis. However, in patients with primary immunodeficiencies (PID), it can lead to severe complications such as severe combined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7de57d504bd663133239d5e2b4970cb9
https://pubmed.ncbi.nlm.nih.gov/33115608
https://pubmed.ncbi.nlm.nih.gov/33115608
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
