Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bijan Varmaghani"'
Autor:
Akbar Dorgalaleh, Muhammad Shahid Shahzad, Mohammad Reza Younesi, Esmaeil Sanei Moghaddam, Mohammad Mahmoodi, Bijan Varmaghani, Zahra Kashani Khatib, Shaban Alizadeh
Publikováno v:
Medical Journal of The Islamic Republic of Iran, Vol 27, Iss 1, Pp 17-22 (2013)
Abstract Backgrounds: G6PD deficiency is the most common enzymopathy of red blood cells. The clinical symptoms of favism are jaundice, hematuria and haemolytic anaemia that seem to affect liver and kidney in long term. Thus we evaluate kidney and liv
Externí odkaz:
https://doaj.org/article/6656a4d463ed48faa81cd396c0c3a680
Publikováno v:
Journal of Cellular and Molecular Anesthesia, Vol 4, Iss 4, Pp 107-111 (2020)
Background: Congenital bleeding disorders (CBD) are a group of coagulopathies with different clinical and laboratory features. The prevalence of these disorders in different parts of the world is variable. Iran as a country with a high rate of parent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::8e4a16e4cec935a9d6b725f004c0d19e
http://journals.sbmu.ac.ir/jcma/article/view/29074
http://journals.sbmu.ac.ir/jcma/article/view/29074
Publikováno v:
Journal of Cellular and Molecular Anesthesia, Vol 1, Iss 4, Pp 154-157 (2016)
Background: Iran has a large group of patients with severe congenital factor XIII deficiency (FXIIID) and Trp187Arg mutation that is most disease causing mutation of FXIII in the world is only observed in southeast of Iran with 352 patients with FXII
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::4720f50bb7940b40d32eb2a2208cfedb
http://journals.sbmu.ac.ir/jcma/article/view/13508
http://journals.sbmu.ac.ir/jcma/article/view/13508
Autor:
Soudabeh Hosseini, Akbar Dorgalaleh, Shadi Tabibian, Aziz Rahimizadeh, Taregh Bamedi, Sharif Ebrahimi, Khanagha Tavakol, Bijan Varmaghani, Morteza Shamsizadeh, Majid Naderi, Shaban Alizadeh
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 26(8)
Factor XIII deficiency (FXIIID) is an extremely rare bleeding disorder with the highest global incidence in southeast of Iran. Southwestern Afghanistan (Nimruz Province) is located near the border with Iran in the vicinity of Sistan and Baluchestan P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e24e0c0070e4b24914759d8406dc321c
https://pubmed.ncbi.nlm.nih.gov/26226252
https://pubmed.ncbi.nlm.nih.gov/26226252
Autor:
Majid, Naderi, Shaban, Alizadeh, Shadi, Tabibian, Soudabeh, Hosseini, Bijan, Varmaghani, Morteza, Shamsizadeh, Akbar, Dorgalaleh
Publikováno v:
Archives of Iranian medicine. 18(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ddc51015e5d1b9d02f23894263d269b
https://pubmed.ncbi.nlm.nih.gov/26155604
https://pubmed.ncbi.nlm.nih.gov/26155604