Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Maryam Gheidishahran"'
Autor:
Zahra Mousavi Kouzehkanan, Sepehr Saghari, Sajad Tavakoli, Peyman Rostami, Mohammadjavad Abaszadeh, Farzaneh Mirzadeh, Esmaeil Shahabi Satlsar, Maryam Gheidishahran, Fatemeh Gorgi, Saeed Mohammadi, Reshad Hosseini
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-14 (2022)
Abstract Accurate and early detection of anomalies in peripheral white blood cells plays a crucial role in the evaluation of well-being in individuals and the diagnosis and prognosis of hematologic diseases. For example, some blood disorders and immu
Externí odkaz:
https://doaj.org/article/bacf88523b6f4478b3411a922e2375f0
Autor:
Samira Pourrezaei, Shahrzad Shadabi, Maryam Gheidishahran, Abbas Rahimiforoushani, Masoume Akhbari, Mahnaz Tavakoli, Mahshid Safavi, Mobina Madihi, Mehdi Norouzi
Publikováno v:
Iranian Journal of Microbiology, Vol 13, Iss 4 (2021)
Background and Objectives: Human T-lymphotropic virus type-1 (HTLV-1) belongs to retrovirus family that causes the neurological disorder HTLV-1 adult T-cell leukemia/lymphoma (ATLL). Since 1980, seven subtypes of the virus have been recognized. HTLV-
Externí odkaz:
https://doaj.org/article/9fa641a4e6ee42b6b88611838d967cf0
Autor:
Kaveh Tari, Pooya Valizadeh Ardalan, Mahnoosh Abbaszadehdibavar, Amir Atashi, Ali Jalili, Maryam Gheidishahran
Publikováno v:
International Journal of Biomedicine and Public Health, Vol 1, Iss 1, Pp 48-58 (2018)
Thalassemia are a group of inherited blood disorders caused by the decrease or absence of beta-globin chain synthesis will be determined with decrease in erythrocyte hemoglobin, decreased production of erythrocytes and anemia. More thalassemia is inh
Externí odkaz:
https://doaj.org/article/9d691e1896874a689e3356045e8a840d
Autor:
Shahrzad Shadabi, Mahnaz Tavakoli, Mahshid Safavi, Masoume Akhbari, Abbas Rahimiforoushani, Mehdi Norouzi, Samira Pourrezaei, Maryam Gheidishahran, Mobina Madihi
Publikováno v:
Iranian Journal of Microbiology
Iranian Journal of Microbiology, Vol 13, Iss 4 (2021)
Iranian Journal of Microbiology, Vol 13, Iss 4 (2021)
Background and Objectives: Human T-lymphotropic virus type-1 (HTLV-1) belongs to retrovirus family that causes the neurological disorder HTLV-1 adult T-cell leukemia/lymphoma (ATLL). Since 1980, seven subtypes of the virus have been recognized. HTLV-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03d4f25ac4047fd88fecb384ee16266a
https://doi.org/10.18502/ijm.v13i4.6976
https://doi.org/10.18502/ijm.v13i4.6976
Autor:
Peyman Rostami, Reshad Hosseini, Esmaeil Shahabi Satlsar, Fatemeh Gorgi, Eslam Tavakoli, Sepehr Saghari, Maryam Gheidishahran, Farzaneh Mirzadeh, Mohammadjavad Abaszadeh, Saeed Mohammadi, Zahra Mousavi Kouzehkanan
Accurate and early detection of peripheral white blood cell anomalies plays a crucial role in the evaluation of an individual's well-being. The emergence of new technologies such as artificial intelligence can be very effective in achieving this. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca633b040d358ea4e17eee7b32d4bfdb
https://doi.org/10.1101/2021.05.02.442287
https://doi.org/10.1101/2021.05.02.442287
Autor:
Mahnoosh Abbaszadehdibavar, Kaveh Tari, Maryam Gheidishahran, Amir Atashi, Pooya Valizadeh Ardalan, Ali Jalili
Publikováno v:
International Journal of Biomedicine and Public Health, Vol 1, Iss 1, Pp 48-58 (2018)
Thalassemia are a group of inherited blood disorders caused by the decrease or absence of beta-globin chain synthesis will be determined with decrease in erythrocyte hemoglobin, decreased production of erythrocytes and anemia. More thalassemia is inh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32b53f0f254e3ca2923e692c97f9156d
http://www.ijbmph.com/article_56102_86f757084a3462c479772468c362d3a1.pdf
http://www.ijbmph.com/article_56102_86f757084a3462c479772468c362d3a1.pdf
Autor:
Esmaeil Sanei Moghaddam, Akbar Dorgalaleh, Majid Naderi, Shadi Tabibian, Fereshte Lotfi, Ahmad Kazeme, Sohaila Khosravi, Majid Safa, Mahmood Shams, Sara Kahraze, Maryam Gheidishahran
Publikováno v:
Blood Coagulation & Fibrinolysis. 29:87-91
Diagnosis of factor XIII (FXIII) deficiency (FXIIID) as a rare bleeding disorder is a challenge worldwide. Thus, in the present study, we used different methods including two molecular methods for detection of FXIIID. This study was conducted on indi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0375fa3bc94388ac35ada665cfbca001
https://doi.org/10.1097/mbc.0000000000000679
https://doi.org/10.1097/mbc.0000000000000679
Autor:
Akbar Dorgalaleh, Shadi Tabibian, Mahmood Shams, Behnaz Tavasoli, Maryam Gheidishahran, Morteza Shamsizadeh
Publikováno v:
Laboratory Medicine. 47:220-226
Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder with an approximately 12-times higher than the rest of the world. The International Society for Thrombosis and Hemostasis (ISTH) suggested a standard algorithm for precise diagnosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea890f284e97492a4a19f7371a676196
https://doi.org/10.1093/labmed/lmw021
https://doi.org/10.1093/labmed/lmw021