Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mehrnoosh Kosaryan"'
Autor:
Javad Ghaffari, Koorosh Vahidshahi, Mehrnoosh Kosaryan, Zahra Soltantooyeh, Mohadese Mohamadi
Publikováno v:
Medicinski Glasnik, Vol 8, Iss 2, Pp 192-196 (2011)
Aim To investigate the humeral immune markers in patients with ß-thalassemia major (TM). Methods In this historical – cohort study (August to December 2007), the case group consisted of 34 TM patients and the control group included the same number
Externí odkaz:
https://doaj.org/article/48076e080434455c803425d1c8727aa3
Autor:
Mehrnoosh Kosaryan
Publikováno v:
Journal of Pediatrics Review, Vol 2, Iss 2, Pp 1-1 (2014)
Externí odkaz:
https://doaj.org/article/42e0673675034ad395f98ff776a1ed64
Autor:
Morteza Alizadeh Forootan, Hosein Karami, Mehrnoosh Kosaryan, Mehdi Ahangari, Koorosh Vahidshahi
Publikováno v:
Hemoglobin. 31:453-462
Beta-thalassemia major (TM) is the most prevalent genetic disease in Mazandaran Province. Currently, about 2,700 TM patients have been registered and are under treatment in the province. This study was undertaken to evaluate the survival of patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a98e2eeb109989599efd8e77d0bbe16
https://doi.org/10.1080/03630260701641294
https://doi.org/10.1080/03630260701641294
Autor:
Mehrnoosh, Kosaryan, Khadijeh, Rabiei
Publikováno v:
Iranian Journal of Psychiatry and Behavioral Sciences
Objective: This study has been done in order to evaluate the papers published in the "Iranian Journal of Psychiatry and Behavioral Sciences" from 2007 to 2010. Methods: A questionnaire was developed according to the design, evidence level, and recomm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8a151d8eaacadc685ea53e31a2e8a0f
https://pubmed.ncbi.nlm.nih.gov/24644513
https://pubmed.ncbi.nlm.nih.gov/24644513
Autor:
Mehrnoosh, Kosaryan, Koorosh, Vahidshahi, Rita, Siami, Meisam, Nazari, Hosein, Karami, Sara, Ehteshami
Publikováno v:
Saudi medical journal. 30(6)
To investigate the knowledge, attitude, and practice of reproductive behavior in Iranian minor thalassemia couples in Ghaemshahr City, Mazandaran, Iran.This is a cross-sectional descriptive survey conducted in 2006. Birth rates from 1997-2005 and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7bd6010436f47d9ee6d5e5f8252cb76c
https://pubmed.ncbi.nlm.nih.gov/19526171
https://pubmed.ncbi.nlm.nih.gov/19526171
Autor:
Ghasemali Khorasani, Mehrnoosh Kosaryan, Koorosh Vahidshahi, Sepideh Shakeri, Mohamad Mehdi Nasehi
Publikováno v:
Hemoglobin. 32(3)
Prevention programs are considered to be a top priority in Iran because beta-thalassemia (beta-thal) major (TM) is the most common autosomal disorder in Iran, and in the Mazandaran Province in particular. The main strategies comprise providing approp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28b6db1a4efae39a039835b9393bb691
https://pubmed.ncbi.nlm.nih.gov/18473242
https://pubmed.ncbi.nlm.nih.gov/18473242
Publikováno v:
Pediatric endocrinology reviews : PER. 2
Osteopenia and osteoporosis are well known complications in beta thalassemia major (TM) patients. Their main cause is bone marrow hyperfunctioning. Hydroxyurea (HU) has recently been used successfully in TM to control ineffective erythropoiesis. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ca5c0fbc05e274617d10ec9e65c565d
https://pubmed.ncbi.nlm.nih.gov/16462716
https://pubmed.ncbi.nlm.nih.gov/16462716