Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Suresh Hanagvadi"'
Autor:
Sujayendra Kulkarni, Rajat Hegde, Smita Hegde, Suyamindra S Kulkarni, Suresh Hanagvadi, Kusal K Das, Sanjeev Kolagi, Pramod B Gai, Rudragouda S Bulagouda
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 11, Iss 6, Pp 2735-2738 (2022)
Background: The most prevalent severe inherited hemorrhagic condition is hemophilia, which means “love of blood.” Hemophilia A and B are caused by a lack or malfunction of the factor VIII and factor IX proteins. Objective: The present study is to
Externí odkaz:
https://doaj.org/article/e6f4e69e89c1416fb5de876a1842b53b
Autor:
Sujayendra Kulkarni, Rajat Hegde, Smita Hegde, Suyamindra S Kulkarni, Suresh Hanagvadi, Kusal K Das, Sanjeev Kolagi, Pramod B Gai, Rudragouda Bulagouda
Publikováno v:
Blood research
Background Hemophilia B (HB) is an X-linked bleeding disorder resulting from coagulation factor IX defects. Over 3,000 pathogenic, HB-associated mutations in the F9 gene have been identified. We aimed to investigate the role of F9 variants in 150 HB
Publikováno v:
Oral oncology. 132
Hemophilia is a hereditary disorder of coagulation that results in deficiency of factor VIII (Hemophilia A) or Factor IX (Hemophilia B) with characteristic X linked mode of inheritance, almost exclusively seen in males while females are asymptomatic
Autor:
Kulkarni, Sujayendra1 (AUTHOR), Hegde, Rajat2 (AUTHOR), Hegde, Smita2 (AUTHOR), Kulkarni, Suyamindra2 (AUTHOR), Hanagvadi, Suresh3 (AUTHOR), Das, Kusal4 (AUTHOR), Kolagi, Sanjeev5 (AUTHOR), Gai, Pramod2 (AUTHOR), Bulagouda, Rudragouda6 (AUTHOR)
Publikováno v:
Journal of Family Medicine & Primary Care. Jun2022, Vol. 11 Issue 6, p2735-2738. 4p.