Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Thalassemia/complications"'
Publikováno v:
Therapeutics and Clinical Risk Management, Vol Volume 18, Pp 259-271 (2022)
Rana Adnan Ahmed,1 Aso Faeq Salih,2 Shirwan Hamasalih Omer,1 Heshu Sulaiman Rahman,1,3 Luqman Khalid Rasool4 1Department of Physiology, College of Medicine, University of Sulaimani, Sulaimaniyah, Republic of Iraq; 2Department of Pediatrics, College o
Externí odkaz:
https://doaj.org/article/a698b926730344ee91cbfbcba409241a
In this survey, we examined the associated complications and conditions of the patients suffering with Beta Thalassemia major. We focused on major factors which can be helpful to critically understand, diagnose and treat this hematological disorder.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b1ed7d219c4a3dee4c0e80fae34da15
Autor:
Diyar Z. Akkaynak, Yeşim Oymak, Gonul Aydogan, Tuğba Gürleyen Eren, Gülsün Karasu, Bahattin Tunç, Fatma Gumruk, Selma Unal, Umran Caliskan, Turkan Patiroglu, Adalet Meral Güneş, Zafer Salcioglu, Ahmet Koç, Yusuf Ziya Aral, Yasemin Isik Balci, Mehmet Akin, Aylin Canbolat Ayhan, Vedat Uygun, Osman Alphan Küpesiz, Gönül Oktay, Canan Vergin, Betül Biner, İlgen Şaşmaz, Mehmet Ertem, Hilmi Apak, Emine Türkkan, Yıldız Yildirmak, Cetin Timur, Elif Güler Kazanci, Gülersu Irken, Ülker Koçak, Murat Söker, Erdal Kurtoğlu, Mehmet Akif Yesilipek, Bülent Antmen, Zeynep Karakas
PubMedID: 30300449 Objectives: To evaluate the long-term efficacy and safety of deferasirox therapy in a large observational cohort of children with transfusion-dependent thalassemia (TDT) and sickle cell anemia (SCA) in Turkey. Methods: This was a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b5a731b446ddb4e25ef6dbad909d7cf
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Autor:
Greene, Makenzie
Thalassemia is one of the most common genetic disorders worldwide and presents major public health and social challenges in areas of high incidence. The frequency of this disorder varies considerably with geographic locations and racial groups. Thala
Akademický článek
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In this study, the authors aimed to evaluate the frequency of pulmonary hypertension (PHT) in asymptomatic thalassemia major (TM) patients, and to investigate the impact of pulmonary function test (PFT) and CO diffusion results on the evaluation of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::9fa08c4ba9e69a5bed0bf83019a3341f
Thalassemia represents the world's most common monogenic disease, characterized by absence of or decreased globin chain production. The lifespan of thalassemia patients has been extended as a result of current supportive treatment. We report three ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::d1f7e7081becd2dc1200eac07f8eed28
http://olympias.lib.uoi.gr/jspui/handle/123456789/20225
http://olympias.lib.uoi.gr/jspui/handle/123456789/20225
Autor:
Argyropoulou, M. I., Astrakas, L.
beta-Thalassaemia major is a hereditary haemolytic anaemia that is treated with multiple blood transfusions. A major complication of this treatment is iron overload, which leads to cell death and organ dysfunction. Chelation therapy, used for iron el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::adf05bd6c15c83e7a15dfe2f9652df7a
http://olympias.lib.uoi.gr/jspui/handle/123456789/19903
http://olympias.lib.uoi.gr/jspui/handle/123456789/19903