Results 61 to 70 of about 495 (105)
Erratum: A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia [PDF]
Kaiqi Jia +6 more
openalex +1 more source
Background: Women and girls with congenital fibrinogen deficiencies (CFDs) face higher hemorrhagic risks during their reproductive years, yet data on gynecologic and obstetric complications remain limited.
Samin Mohsenian +17 more
doaj +1 more source
A novel fibrinogen gamma-chain mutation, p. γAla327Val, causes structural abnormality of D region and ultimately leads to congenital dysfibrinogenemia [PDF]
Aiqiu Wei +6 more
openalex +1 more source
A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia [PDF]
Kaiqi Jia +6 more
openalex +1 more source
Dysfibrinogenemia with Subgaleal Hematoma: An Unusual Presentation [PDF]
Manika Khare +4 more
openalex +1 more source
Dysfibrinogenemia during pregnancy treated successfully with fibrinogen [PDF]
Yoshihiko Yamanaka +5 more
openalex +1 more source
Fibrinogen Šumperk II: Dysfibrinogenemia in an individual with two coding mutations [PDF]
Roman Kotlín +5 more
openalex +1 more source

