Clinical features and management of congenital fibrinogen deficiencies
A Casini, P de Moerloose… - Seminars in thrombosis …, 2016 - thieme-connect.com
Congenital fibrinogen disorders are rare diseases affecting either the quantity
(afibrinogenemia and hypofibrinogenemia) or the quality (dysfibrinogenemia) or both …
(afibrinogenemia and hypofibrinogenemia) or the quality (dysfibrinogenemia) or both …
Molecular basis of rare congenital bleeding disorders
A Dorgalaleh, M Bahraini, M Shams, F Parhizkari… - Blood Reviews, 2023 - Elsevier
Rare bleeding disorders (RBDs), including factor (F) I, FII, FV, FVII, combined FV and FVIII
(CF5F8), FXI, FXIII and vitamin-K dependent coagulation factors (VKCF) deficiencies, are a …
(CF5F8), FXI, FXIII and vitamin-K dependent coagulation factors (VKCF) deficiencies, are a …
Thromboembolism in patients with congenital afibrinogenaemia
M Nagler, JAK Hovinga, L Alberio… - Thrombosis and …, 2016 - thieme-connect.com
Frequent arterial and venous thromboembolism in patients with congenital
afibrinogenaemia (CA) is neither understood nor is a safe and effective treatment …
afibrinogenaemia (CA) is neither understood nor is a safe and effective treatment …
Pharmacological management of rare coagulation factor deficiencies besides hemophilia
Introduction Rare coagulation factor deficiencies are less-known disorders with variable
effects on the patient's life. Management of such patients is a challenge due to the paucity of …
effects on the patient's life. Management of such patients is a challenge due to the paucity of …
Regulation of fibrinogen synthesis
D Dre'Von A, R Fish, PS de Vries, AC Morrison… - Thrombosis …, 2024 - Elsevier
The plasma protein fibrinogen is encoded by 3 structural genes (FGA, FGB, and FGG) that
are transcribed to mRNA, spliced, and translated to 3 polypeptide chains (Aα, Bβ, and γ …
are transcribed to mRNA, spliced, and translated to 3 polypeptide chains (Aα, Bβ, and γ …
Resolution of fibrinogen deficiency in a patient with congenital afibrinogenemia after liver transplantation.
N Gallastegui, EL Kimble, TJ Harrington - Haemophilia, 2016 - search.ebscohost.com
The article reports a case of subsequent resolution of fibrinogen deficiency and restoration
of haemostasis in a 25-year-old woman with congenital afibrinogenemia after orthotopic …
of haemostasis in a 25-year-old woman with congenital afibrinogenemia after orthotopic …
遗传性无纤维蛋白原血症1 例临床及基因分析
张兴道， 曹海燕， 原新慧， 李宇宁 - 2019 - ir.lzu.edu.cn
摘要目的探讨遗传性无纤维蛋白原血症的临床特点及遗传学特征. 方法回顾分析1
例遗传性无纤维蛋白原血症患儿的临床资料, 并复习相关文献. 结果男性患儿 …
例遗传性无纤维蛋白原血症患儿的临床资料, 并复习相关文献. 结果男性患儿 …
Nörofibromatozisli hastalarda görülen atrofik skar ile yara iyileşmesi ve ekstrasellüler matriks elemanlarının ilişkileri, nörofibromlu dokudaki damar endoteli ve damar …
OÜ Demir - acikbilim.yok.gov.tr
Nörofibromatozis tip I (NF-I),café-au-laitlekeleri ve nörofibromlarla karakterize otozomal
dominant bir bozukluktur. Vasküler NF-1 lezyonları, çevredeki kan damarları ve yumuşak …
dominant bir bozukluktur. Vasküler NF-1 lezyonları, çevredeki kan damarları ve yumuşak …