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Hypodysfibrinogenemia
Rare Thrombophilic Conditions
Identification of Three Novel Fibrinogen Gamma Chain Mutations
Fibrinogen Maracaibo: Hypo-Dysfibrinogenemia Caused
Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders
A Case of Hypofibrinogenemia Presenting with Submental Hamatoma
Rare Coagulation Disorder Patient Information
Congenital Structural and Functional Fibrinogen Disorders: a Primer for Internists
Congenital Hypofibrinogenemia Detected During Preoperative Workup for Major Cardiac Surgery
Diagnosis and Management of Heavy Menstrual Bleeding and Bleeding Disorders in Adolescents
Thrombosis Panel (Test Code 4820) Please Complete All Pages of the Mammalian Plasma
FGG Gene Fibrinogen Gamma Chain
Rare Coagulopathies Chapter 5 Author
The Rare Bleeding Disorders
Fibrinogen Philadelphia. a Hereditary Hypodysfibrinogenemia Characterized by Fibrinogen Hypercatabolism
Thrombosis in Inherited Fibrinogen Disorders
Scientific Programme Sunday, 12. July 2020 Plenary Session State-Of-The-Art on Hemophilia and Rare Bleeding Disorders State-Of-T
Diagnosis and Classification of Congenital Fibrinogen Disorders Fibrinogen and FXIII SSC
Congenital Fibrinogen Disorders: an Update
Top View
Looking at the Dark Face of the Thrombosis
Rare Bleeding Disorders
Diagnosis and Treatment of Von Willebrand Disease and Rare Bleeding Disorders
Increased Plasma Clot Permeability and Susceptibility to Lysis Are Associated with Heavy Menstrual Bleeding of Unknown Cause: a Case-Control Study
Increased Plasma Clot Permeability and Susceptibility to Lysis Are Associated with Heavy Menstrual Bleeding of Unknown Cause: a Case-Control Study
Hypodysfibrinogenemia in a Young Patient with Recurrent Strokes
Thrombosis in Inherited Fibrinogen Disorders
Constitutional Hypofibrinogenemia Associated with Third Trimester Hemorrhage* D
What Are Rare Clotting Factor Deficiencies?
FGA Gene Fibrinogen Alpha Chain
Accepted Version
Fibrinogen Baltimore II: Congenital Hypodysfibrinogenemia with Delayed Release of Fibrinopeptide- B and Decreased Rate of Fibrin