Výsledky vyhledávání

Clinical outcome of interferon and ribavirin combination treatment in hepatitis C virus infected patients with congenital bleeding disorders in Iran

Autor: M. N. Toosi, M. Rasoulzadegan, F. Ala, Mahboubeh Rahmani, G. R. Lari, M. Jazebi, K. Ghannadi

Publikováno v: Haemophilia. 15:1097-1103

Summary. Hepatitis C virus (HCV) infection is a major cause of morbidity and mortality in patients with inherited bleeding disorders. The results of interferon and ribavirin combination therapy have been reported in a limited number of clinical trial

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e004bf6d82af60808cf83e864312a58b
https://doi.org/10.1111/j.1365-2516.2009.02042.x

Zobrazit plný text záznamu

Seven novel point mutations in the F11 gene in Iranian FXI-deficient patients

Autor: Mojgan Allahyari, S. Ravanbod, Pezhman Fard-Esfahani, M. Rassoulzadegan, G. R. Lari, F. Ala, F. Mirkhani

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 14(1)

Summary. Factor XI (FXI) deficiency disorder is caused by defects in the F11 gene. The affected patients may suffer unexpected and major bleeding after trauma. Hence, the aim of this study was to identify the mutations underlying FXI deficiency in Ir

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab522974e349150f320aed4456c6bb9e
https://pubmed.ncbi.nlm.nih.gov/18005151

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání