Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Sima Zolfaghari"'
Autor:
Matteo De Chiara
Publikováno v:
Abstracta Iranica.
Cet ouvrage porte sur la description linguistique et anthropologique des Bakhtiaris, population chiite, en partie nomade, repandue en Iran entre les villes d’Esfahān et Ahvaz, dans le Khuzestān et le Lorestān, entre autres. Le bakhtiari est une
Autor:
Mojgan Shaiegan, Mostafa Moghaddam, Mahtab Maghsudlu, Azita Azarkeivan, Sima Zolfaghari, Ali-Akbar Pourfatollah, Peyman Soleimanzadeh, Ehsan Shahverdi
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 16, Iss 1 (2022)
Background: An analysis of red blood cell alloimmunization in patients with thalassemia can help to devise specific strategies to decrease the alloimmunization rate. This study explored the frequency and specificity of alloantibodies and autoantibodi
Externí odkaz:
https://doaj.org/article/3e7a9a02b198429ab63828ad14879120
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 18, Iss 7, Pp 627-634 (2015)
Objective(s):Human cytomegalovirus (CMV), a double-strand DNA herpesvirus, can be transmitted via blood transfusion which is especially important for immunocompromised recipients and can cause a fatal infection. CMV seroprevalence in Iran was studied
Externí odkaz:
https://doaj.org/article/3c6f88ed4d8f486ea74741e0dcdc801e
Autor:
Sima Zolfaghari, Ole Jørgen Kaasbøll, Vivi T. Monsen, Bojana Sredic, Else Marie V. Hagelin, Håvard Attramadal
Publikováno v:
The Journal of biological chemistry.
Cellular Communication Network (CCN) proteins have multimodular structures important for their roles in cellular responses associated with organ development and tissue homeostasis. CCN2 has previously been reported to be secreted as a preproprotein t
Autor:
Else Marie Valbjørn Hagelin, Fabian A. Line, Vivi T. Monsen, M. Shakil Ahmed, Håvard Attramadal, Ole Jørgen Kaasbøll, Sima Zolfaghari
Publikováno v:
Journal of cell communication and signaling. 16(3)
CCN5 is a divergent member of the cellular communication network factor (CCN) family in that it lacks the carboxyl terminal cystine knot domain common to the other CCN family members. CCN5 has been reported to antagonize the profibrotic actions of CC
Autor:
Mojgan Shaiegan, Mostafa Moghaddam, Mahtab Maghsudlu, Azita Azarkeivan, Sima Zolfaghari, Ali-Akbar Pourfatollah, Peyman Soleimanzadeh, Ehsan Shahverdi
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 16, Iss 1 (2022)
Background: An analysis of red blood cell alloimmunization in patients with thalassemia can help to devise specific strategies to decrease the alloimmunization rate. This study explored the frequency and specificity of alloantibodies and autoantibodi
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:
Mahin Nikougoftar, Minoo Ahmadinejad, Sima Zolfaghari, Mohammad Reza Deyhim, Akbar Hashemi Tayer, Naser Amirizadeh
Publikováno v:
Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie. 46(4)
Background: Red blood cells (RBCs) undergo structural and biochemical alterations during storage which are collectively called RBC storage lesion and cause a decrease in RBC recovery and survival. During storage, erythrocytes release an increasing nu
Publikováno v:
Transfusion and Apheresis Science. 53:38-47
Background Evaluation of trends in the rate of transfusion-transmitted infections (TTIs) in blood donors is essential for monitoring blood supply safety and donor screening effectiveness. The aim of this study was to determine the trends and prevalen
Publikováno v:
Journal of Hematology. 4:210-213
Hyperhemolysis syndrome (HS) is a delayed type of transfusion reactions (DTHRs). These may occur in patients with hemoglobinopathies due to destruction of red blood cells (RBCs). A 17-year-old boy with B-thalassemia and a history of multiple transfus