Zobrazeno 1 - 10
of 705
pro vyhledávání: '"A. Azarkeivan"'
Autor:
M. Karimi, T. Zarei, S. Haghpanah, A. Azarkeivan, M. Naderi, S. Matin, A. Bazrafshan, Z. Zahedi, A. Shirkavand, P. Pishdad, V. De Sanctis
Publikováno v:
HemaSphere, Vol 6, Pp 2100-2101 (2022)
Externí odkaz:
https://doaj.org/article/425cb3135cb8415ba2680459c9e247ef
Publikováno v:
BMC Research Notes, Vol 17, Iss 1, Pp 1-7 (2024)
Abstract Purpose This study aimed to evaluate the knowledge, attitude, and practice toward iron chelating agents (ICAs) in Iranian thalassemia major patients. Methods A total of 101 patients with thalassemia major were involved in this cross-sectiona
Externí odkaz:
https://doaj.org/article/d62dd69dd16446feb41c2632369a61dd
Autor:
Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi
Publikováno v:
npj Genomic Medicine, Vol 9, Iss 1, Pp 1-11 (2024)
Abstract Next-generation sequencing (NGS) has been proven to be one of the most powerful diagnostic tools for rare Mendelian disorders. Several studies on the clinical application of NGS in unselected cohorts of Middle Eastern patients have reported
Externí odkaz:
https://doaj.org/article/d0de56f0485d43639ba3ed001723c22f
Publikováno v:
Reviews in Clinical Medicine, Vol 10, Iss 4, Pp 50-57 (2023)
Introduction: Multi-organ iron load is prevalent crucial side effect in thalassemic patients due to repeated transfusions, and high intestinal iron absorption. MRI T2* has demonstrated its potency as a non-invasive technique for the imaging of hemosi
Externí odkaz:
https://doaj.org/article/654f41e790d747ce87905e381a33c888
Publikováno v:
Reviews in Clinical Medicine, Vol 10, Iss 3, Pp 30-35 (2023)
Introduction: Thalassemia consists of a variety of genetic hemoglobinopathies. Thalassemia-major causes anemia in early age. Those suffering from thalassemia need frequent life-long blood transfusions to survive, resulting in iron overload in the bod
Externí odkaz:
https://doaj.org/article/45134d05c4d04971b7025bb1550ca3d4
Autor:
Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101510- (2024)
Externí odkaz:
https://doaj.org/article/2b6cd8a2516d4c7dba834e7f5dd8bf1b
Akademický článek
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Autor:
Mohammad Faranoush, Pooya Faranoush, Iraj Heydari, Mohammad Reza Foroughi‐Gilvaee, Azita Azarkeivan, Ali Parsai Kia, Negin Sadighnia, Ali Elahinia, Afsoon Zandi, Mohammad Reza Rezvany, Nahid Hashemi‐Madani, Amir Ziaee, Reza Nekouian, Farzaneh Rohani
Publikováno v:
Health Science Reports, Vol 6, Iss 10, Pp n/a-n/a (2023)
Abstract Background and Aims One of the most common hemoglobinopathies globally related to blood transfusion and iron overload in the body is thalassemia syndrome. Increasing ferritin levels can cause severe damage to the patient's body organs. This
Externí odkaz:
https://doaj.org/article/071fd354e4d0401484f93b25dc05efd6
Publikováno v:
In Transfusion clinique et biologique May 2023 30(2):205-211
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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