Zobrazeno 1 - 10
of 453
pro vyhledávání: '"Asghar Aghamohammadi"'
Autor:
Yasser Bagheri, Tannaz Moeini Shad, Shideh Namazi, Farzaneh Tofighi Zavareh, Gholamreza Azizi, Fereshteh Salami, Somayeh Sadani, Ali Hosseini, Mohsen Saeidi, Salar Pashangzadeh, Samaneh Delavari, Babak Mirminachi, Nima Rezaei, Hassan Abolhassani, Asghar Aghamohammadi, Reza Yazdani
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-12 (2023)
Abstract Background Selective IgA deficiency (SIgAD) is the most prevalent inborn errors of immunity with almost unknown etiology. This study aimed to investigate the clinical diagnostic and prognostic values of lymphocyte subsets and function in sym
Externí odkaz:
https://doaj.org/article/f6b40903cde84cfcb92e115edd55098b
Autor:
Marzieh Heidarzadeh Arani, Reza ArefNezhad, Javad Fathgharib, Asghar Aghamohammadi, Hossein Motedayyen
Publikováno v:
Clinical Case Reports, Vol 9, Iss 1, Pp 556-559 (2021)
Abstract Ataxia‐telangiectasia (A‐T) is known as an uncommon autosomal recessive disorder associated with recurrent infections and other clinical complications. The management of its complications can improve life quality of patients.
Externí odkaz:
https://doaj.org/article/620d881fc4464e09bc8809e02c4e02f0
Autor:
Negar Moradian, Hans D. Ochs, Constantine Sedikies, Michael R. Hamblin, Carlos A. Camargo, J. Alfredo Martinez, Jacob D. Biamonte, Mohammad Abdollahi, Pedro J. Torres, Juan J. Nieto, Shuji Ogino, John F. Seymour, Ajith Abraham, Valentina Cauda, Sudhir Gupta, Seeram Ramakrishna, Frank W. Sellke, Armin Sorooshian, A. Wallace Hayes, Maria Martinez-Urbistondo, Manoj Gupta, Leila Azadbakht, Ahmad Esmaillzadeh, Roya Kelishadi, Alireza Esteghamati, Zahra Emam-Djomeh, Reza Majdzadeh, Partha Palit, Hamid Badali, Idupulapati Rao, Ali Akbar Saboury, L. Jagan Mohan Rao, Hamid Ahmadieh, Ali Montazeri, Gian Paolo Fadini, Daniel Pauly, Sabu Thomas, Ali A. Moosavi-Movahed, Asghar Aghamohammadi, Mehrdad Behmanesh, Vafa Rahimi-Movaghar, Saeid Ghavami, Roxana Mehran, Lucina Q. Uddin, Matthias Von Herrath, Bahram Mobasher, Nima Rezaei
Publikováno v:
Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-7 (2020)
Abstract The COVID-19 pandemic has become the leading societal concern. The pandemic has shown that the public health concern is not only a medical problem, but also affects society as a whole; so, it has also become the leading scientific concern. W
Externí odkaz:
https://doaj.org/article/120cd09ce7fa494abb4748f3b788a015
Autor:
Asghar Aghamohammadi, Mohammadreza Shaghaghi, Hassan Abolhassani, Reza Yazdani, Seyed Mohsen Zahraie, Mohammad Mehdi Goya, Susan Mahmoudi, Nima Rezaei, Shohreh Shahmahmoodi
Publikováno v:
Tehran University Medical Journal, Vol 78, Iss 1, Pp 1-8 (2020)
Primary immunodeficiency diseases (PIDs) is a diverse group of diseases, characterized by a defect in the immune system. These patients are susceptible to recurrent respiratory infections, gastrointestinal problems, autoimmune diseases, and malignanc
Externí odkaz:
https://doaj.org/article/dc7407553e7a470db690cf94d98783fa
Autor:
Tannaz Moeini Shad, Reza Yazdani, Parisa Amirifar, Samaneh Delavari, Marzieh Heidarzadeh Arani, Seyed Alireza Mahdaviani, Mahnaz Sadeghi-Shabestari, Asghar Aghamohammadi, Nima Rezaei, Hassan Abolhassani
Publikováno v:
Frontiers in Immunology, Vol 12 (2022)
Ataxia-telangiectasia (AT) is a rare autosomal recessive neurodegenerative multisystem disorder. A minority of AT patients can present late-onset atypical presentations due to unknown mechanisms. The demographic, clinical, immunological and genetic d
Externí odkaz:
https://doaj.org/article/bc09feba54124673bcf9b84e5d028108
Autor:
Mohammadreza Shaghaghi, Shohreh Shahmahmoodi, Ali Nili, Hassan Abolhassani, Seyedeh Panid Madani, Ahmad Nejati, Maryam Yousefi, Yaghoob M. Kandelousi, Mona Irannejad, Shiva Shaghaghi, Seyed Mohsen Zahraei, Sussan Mahmoudi, Mohammad Mehdi Gouya, Reza Yazdani, Gholamreza Azizi, Nima Parvaneh, Asghar Aghamohammadi
Publikováno v:
Emerging Infectious Diseases, Vol 25, Iss 11, Pp 2005-2012 (2019)
Patients with immunodeficiency-associated vaccine-derived poliovirus (iVDPV) are potential poliovirus reservoirs in the posteradication era that might reintroduce polioviruses into the community. We update the iVDPV registry in Iran by reporting 9 ne
Externí odkaz:
https://doaj.org/article/ea5873ac693b4b5b9aba9835e4e348e6
Autor:
Zahra Hamidi Esfahani, Reza Yazdani, Sepideh Shahkarami, Fateme Babaha, Hassan Abolhassani, Maryam Sadr, Ali Akbar Pourfathollah, Asghar Aghamohammadi
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 6 (2021)
Common variable immunodeficiency (CVID) is the most prevalent form of symptomatic primary humoral immunodeficiencies characterized by failure in the final differentiation of B lymphocytes. The majority of CVID cases have no identified genetic defect,
Externí odkaz:
https://doaj.org/article/6cfbbfef2b4a4197a7ba1405fef2397f
Autor:
Zahra Shahbazi, Nima Parvaneh, Shirin Shahbazi, Hamzeh Rahimi, Mohammad Hamid, Davoud Shahbazi, Samaneh Delavari, Hassan Abolhassani, Asghar Aghamohammadi, Reza Mahdian
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 15, Iss 1, Pp 1-9 (2019)
Abstract Background The lymphohematopoietic cells originating from feto-maternal trafficking during pregnancy may cause microchimerism and lead to materno-fetal graft versus host disease (GVHD) in severe combined immunodeficiency (SCID) patients. How
Externí odkaz:
https://doaj.org/article/486251d0c4734d078ed98af6b1a0d227
Autor:
Asghar Aghamohammadi, Seyed M. Akrami, Marjan Yaghmaie, Nima Rezaei, Gholamreza Azizi, Mehdi Yaseri, Hassan Nosrati, Majid Zaki-Dizaji
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 18, Iss 4, Pp 440-446 (2019)
Objectives: Ataxia-telangiectasia (A-T) is an autosomal recessive multisystem disorder characterised by cerebellar degeneration, telangiectasia, radiation sensitivity, immunodeficiency, oxidative stress and cancer susceptibility. Epidemiological rese
Externí odkaz:
https://doaj.org/article/ae5d3098737144299369b98536a924c5
Autor:
Asghar Aghamohammadi, Majid Keivanfar, Safoura Navaei, Rohola Shirzadi, Farzad Masiha, Zahra Allameh, Amin Heydari, Solat Eslami, Gholamreza Azizi, Mohsen Reisi, Mohammadreza Modaresi
Publikováno v:
Acta Medica Iranica, Pp 33-41 (2019)
Cystic fibrosis (CF), as a fatal genetic condition, is associated with high morbidity and mortality rates. In Iran, limited studies exist on this disease. This study aims to compare the demographic, clinical and paraclinical data of CF patients. This
Externí odkaz:
https://doaj.org/article/bab0d1110a344365b4f3ed26f4397dc4