Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Razieh Hantooshzadeh"'
Autor:
Parisa Mohseni, Azimeh Khodami, Fatemeh Malek, Ayad Bahadorimonfared, Koorosh Etemad, Mohammad Aghighi, Sahar Sotoodeh Ghorbani, Razieh Hantooshzadeh, Mahmoud Hajipour, Fatemeh Kheiry, Niloufar Taherpour, Negar Piri, Tannaz Valadbeigi
Publikováno v:
Hemoglobin. 45:245-249
The β-thalassemias are a group of genetic disorders defined by decreased levels of functional hemoglobin (Hb). In light of pivotal improvements in patient survival, the load of consistent treatment harms patients' quality of life (QOL). This study a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38ed4694f5d420457cf52ddefc8859e2
https://doi.org/10.1080/03630269.2021.1965617
https://doi.org/10.1080/03630269.2021.1965617
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis
Establishing an appropriate prophylaxis regimen for children with hemophilia is a critical challenge in developing countries. Barriers including availability and affordability, catheter-related complications, and inhibitor development risks have led
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6afbfab5f9b32877c4d3bcf81baf7ed3
http://europepmc.org/articles/PMC6714659
http://europepmc.org/articles/PMC6714659
Autor:
Sezaneh Haghpanah, Azin Hamidi, Mehran Karimi, Marzieh Bardestani, Maryam Khavari, Mohammad Hadi Bagheri, Razieh Hantooshzadeh
Publikováno v:
Iranian Red Crescent Medical Journal
Background: Recent studies regarding the effect of hydroxyurea (HU) in thalassemia have revealed favorable effects on the reduction of ineffective erythropoiesis. Objectives: The aim of the current study was to evaluate whether or not HU can have an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9256fa74364510b2ea18057bf3fdb867
http://europepmc.org/articles/PMC4166105
http://europepmc.org/articles/PMC4166105