Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Mohammad Ali Jalali Far"'
Publikováno v:
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, Vol 31, Iss 1, Pp 6278-6285 (2023)
Introduction: Due to the pathophysiology of Sickle cell disease (SCD), several treatment strategies have been reviewed so far. One of the strategies is anti-sickling factors. This study was performed to determine the effect of methanolic extract of C
Externí odkaz:
https://doaj.org/article/75048353368747a69714e82aa5c6b906
Autor:
Mohammad Ali Jalali Far, Arezoo Oodi, Naser Amirizadeh, Mahshid Mohammadipour, Bijan Keikhaei Dehdezi
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Abstract Introduction The alloimmunization following blood transfusion can be life‐threatening. The Rh alloantibodies are one of the most common causes contributing to alloimmunization. This study aimed to evaluate the rate and causes of alloimmuni
Externí odkaz:
https://doaj.org/article/667b5173a9514fe3983d90fd4fb50003
Autor:
Mohammad Ali Jalali Far, Ali Dehghani Fard, Saiedeh Hajizamani, Majid Mossahebi-Mohammadi, Hamid Yaghooti, Najmaldin Saki
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 10, Iss 1 (2016)
Background: Efficient induction of fetal hemoglobin (HbF) is considered as an effective therapeutic approach in beta thalassemia. HbF inducer agents can induce the expression of γ-globin gene and produce high levels of HbF via different epigenetic a
Externí odkaz:
https://doaj.org/article/bef6c0aa43ef4460b0f812e52c417b23
Autor:
Elham Rajaei, Behnam Sheibani, Mandana Pouladzadeh, Parastoo Moradi Choghakabodi, Mehdi Safdarian, Abdolaziz Feghhi, Alireza Ghorbani bavani, Mehdi Torabizadeh, Gholam Abbas Kaydani, Arash Forouzan, Mohammad Ali Jalali Far, Peyman Eshghi, Mansour Amin, Farid Yousefi, Reza Hadaddezfuli, Hassan Abolghasemi, Mehri Ghafourian Boroujerdnia
Publikováno v:
Internal and Emergency Medicine
Evaluating the effect of convalescent plasma (CP) on some cytokine storm indices in severe COVID-19 patients. Totally, 62 patients were randomly assigned into two groups for this clinical trial. Patients in the intervention group received one unit (5
Publikováno v:
SN Comprehensive Clinical Medicine. 1:1060-1064
Thalassemia is the most common congenital hemolytic disorder by a partial or complete deficiency in globin chain synthesis. Recent investigations have suggested a correlation between protein Z (PZ) and protein Z-dependent protease inhibitor (ZPI) def
Autor:
Mahshid Mohammadipour, Naser Amirizadeh, Bijan Keikhaei Dehdezi, Arezoo Oodi, Mohammad Ali Jalali Far
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Introduction The alloimmunization following blood transfusion can be life‐threatening. The Rh alloantibodies are one of the most common causes contributing to alloimmunization. This study aimed to evaluate the rate and causes of alloimmunization an
Autor:
Parastoo Moradi, Choghakabodi, Mandana, Pouladzadeh, Habib, Haybar, Bijan, Keikhaei, Khojasteh, Hossein Nezhad, Mohammad Ali, Jalali Far, Masoud, Torabpour
Publikováno v:
Recenti progressi in medicina. 111(7)
Riassunto. L'ischemia miocardica silente (SMI) è un aspetto dello spettro della cardiopatia ischemica che varia dalla malattia coronarica asintomatica all'angina grave. Considerando il progressivo aumento della prevalenza di SMI e l'inaffidabilità
Autor:
Omid Kiani Ghaleh Sardi, Mostafa Paridar, Mohammad-Ali Jalali-Far, Abbas Khosravi, Sima Zolfaghari, Mehdi Sajadi
Publikováno v:
Frontiers in Biology. 13:226-234
The determination of the role of mobile sites, as compared with fixed sites, in providing safe blood supply will help with the planning of future programs. This retrospective study was carried out at the Khuzestan Blood Transfusion Organization from
Autor:
Kavianpour, Maria1, Mohammad Ali Jalali Far1, Asl, Javad Mohammadi2, Ahmadzadeh, Ahmad1, Vosughi, Tina1, Ketabchi, Neda1, Saki, Najmaldin1 najmaldinsaki@gmail.com
Publikováno v:
Clinical Cancer Investigation Journal. Jan-Feb2017, Vol. 6 Issue 1, p86-91. 6p.
Publikováno v:
APMIS. 125:1042-1055
Immune Thrombocytopenic Purpura (ITP) is a common autoimmune bleeding disorder characterized by a reduction in peripheral blood platelet counts. In this disease, autoantibodies (Auto-Abs) are produced against platelet GPIIb/GPIIIa by B cells, which r