Results 61 to 70 of about 495 (105)

Erratum: A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia [PDF]

open access: bronze, 2023
Kaiqi Jia   +6 more
openalex   +1 more source

Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database

open access: yesResearch and Practice in Thrombosis and Haemostasis
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

PB0209 Clinical Manifestations of Patients with Congenital Dysfibrinogenemia with the Most Common Hotspot Mutation in FGA Gene p.Arg35His

open access: gold, 2023
Tomáš Šimurda   +10 more
openalex   +1 more source

Poster Sessions

open access: yes
HemaSphere, Volume 9, Issue S1, June 2025.
wiley   +1 more source

A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia [PDF]

open access: bronze, 2023
Kaiqi Jia   +6 more
openalex   +1 more source

Publication Only

open access: yes
HemaSphere, Volume 9, Issue S1, June 2025.
wiley   +1 more source

Dysfibrinogenemia with Subgaleal Hematoma: An Unusual Presentation [PDF]

open access: bronze, 2015
Manika Khare   +4 more
openalex   +1 more source

Dysfibrinogenemia during pregnancy treated successfully with fibrinogen [PDF]

open access: bronze, 2003
Yoshihiko Yamanaka   +5 more
openalex   +1 more source

Fibrinogen Šumperk II: Dysfibrinogenemia in an individual with two coding mutations [PDF]

open access: bronze, 2012
Roman Kotlín   +5 more
openalex   +1 more source

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