Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Roza kamfiroozi"'
Autor:
Mohammadreza Bordbar, Mehdi Pasalar, Sanaz Safaei, Roza kamfiroozi, Sohelia Zareifar, Omidreza zekavat, Sezaneh Haghpanah
Publikováno v:
Journal of Traditional and Complementary Medicine, Vol 8, Iss 1, Pp 141-146 (2018)
This study aimed to determine the frequency and pattern of complementary and alternative medicine (CAM) use in thalassemia patients in south of Iran. The survey was done using a validated questionnaire which was distributed among 122 thalassemia pati
Externí odkaz:
https://doaj.org/article/27536121b97f4fd39bb2c0dd640d01bc
Autor:
Roza Kamfiroozi, Sezaneh Haghpanah, Fatemeh Amirmoezi, Maryam Araghizadeh, Zahra Mohebbinia, Mohammadreza Bordbar
Publikováno v:
International Journal of Cancer Management. 10
Background: Use of complementary and alternative medicine (CAM) among cancer patients is not exactly defined. Objectives: The aim of this study was to determine the use of CAM and associated factors among Iranian cancer patients, reasons behind this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::751804ae3fcdf949fd525158f44399cf
https://doi.org/10.5812/ijcm.7233
https://doi.org/10.5812/ijcm.7233
Autor:
Sohelia Zareifar, Mehdi Pasalar, Sanaz Safaei, Mohammadreza Bordbar, Roza Kamfiroozi, Omidreza Zekavat, Sezaneh Haghpanah
Publikováno v:
Journal of Traditional and Complementary Medicine
Journal of Traditional and Complementary Medicine, Vol 8, Iss 1, Pp 141-146 (2018)
Journal of Traditional and Complementary Medicine, Vol 8, Iss 1, Pp 141-146 (2018)
This study aimed to determine the frequency and pattern of complementary and alternative medicine (CAM) use in thalassemia patients in south of Iran. The survey was done using a validated questionnaire which was distributed among 122 thalassemia pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd4c90e120cc9e41215728c75ac8ff70
https://pubmed.ncbi.nlm.nih.gov/29322002
https://pubmed.ncbi.nlm.nih.gov/29322002
Autor:
Roza Kamfiroozi, Samir Silavizadeh, Marzieh Bardestani, Mohammadreza Bordbar, Sezaneh Haghpanah, Mehran Karimi
Publikováno v:
Iranian Red Crescent Medical Journal
Background: β-Thalassemia is an inherited hemoglobin disorder caused by defective synthesis of s-globin chains. Hemoglobin (Hb) F induction is a possible therapeutic approach which can partially compensate for α and non-α globin chains imbalance.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf32e6da0075b6b55fc80aa2f283dd41
http://europepmc.org/articles/PMC4102988
http://europepmc.org/articles/PMC4102988