Page last updated: 2024-08-26

fibrinogen and Blood Coagulation Factor Deficiencies

fibrinogen has been researched along with Blood Coagulation Factor Deficiencies in 26 studies

Research

Studies (26)

TimeframeStudies, this research(%)All Research%
pre-19901 (3.85)18.7374
1990's0 (0.00)18.2507
2000's17 (65.38)29.6817
2010's8 (30.77)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Era, S; Maeda, H; Matsunaga, S; Nakamura, E; Ono, Y; Seki, H; Takai, Y; Yamamoto, K1
Banerjee, A; Cohen, MJ; Coleman, JR; Colvis, A; Ghasabyan, A; Moore, EE; Moore, HB; Nunns, GR; Sauaia, A; Silliman, CC; Stettler, GR1
Chang, HJ; Choi, HS; Kim, BC; Kim, DY; Kim, SY; Oh, JH; Park, JW; Park, SC; Son, HJ1
Adelmann, D; Illievich, UM; Klaus, DA; Kozek-Langenecker, S; Krall, C; Krenn, CG; Schaden, E1
Ackroyd, S; Alikhan, R; Bowles, L; Chowdary, P; Grainger, J; Mainwaring, J; Mathias, M; Mumford, AD; O'Connell, N1
Menegatti, M; Peyvandi, F1
Weisel, JW1
Dyr, JE; Hirmerová, J; Kotlín, R; Malý, M; Reicheltová, Z; Riedel, T; Salaj, P; Sobotková, A; Suttnar, J1
Atkinson, JP; Hourcade, DE; Liszewski, MK1
Kitchen, S; Woolley, A1
Hamano, A; Madoiwa, KS; Matsuda, M; Mimuro, J; Sakata, Y; Sugo, T; Tanaka, T1
Arocha-Piñango, CL; de Bosch, N; Marchi, R; Meyer, M; Soria, J; Weisel, JW1
Cohen, BM; Cohen, E; Nielsen, VG1
Castaman, G; Duga, S; Ghiotto, R; Rodeghiero, F1
Benavides Márquez, F; Flor Serra, F; Peña Sendra, E; Rodríguez Cristóbal, JJ; Travé Mercadé, P; Villaverde Grote, C1
Arana, C; Cutando-Soriano, A; Gómez-Moreno, G; Scully, C1
Brimhall, B; Le, T; Sidhu, RS; Thompson, H1
Al-Mondhiry, HA; Farrell, DH; Flood, VH1
Dardik, R; Savion, N; Shenkman, B; Tamarin, I; Varon, D1
Brooks, MB; Erb, HN; Stokol, T1
Chan, JC1
Sahud, M1
Makris, M; Vora, A1
Amadei, N; Baracho, GV; Bastos, W; Florido, MP; Isaac, L; Nudelman, V1
Dechavanne, M; Ffrench, P; Hanss, M; Négrier, C; Sobas, F; Trzeciak, MC1
Coller, BS; Gralnick, HR; Sultan, Y1

Reviews

5 review(s) available for fibrinogen and Blood Coagulation Factor Deficiencies

ArticleYear
Treatment of rare factor deficiencies in 2016.
    Hematology. American Society of Hematology. Education Program, 2016, Dec-02, Volume: 2016, Issue:1

    Topics: Blood Coagulation Factors; Blood Component Transfusion; Coagulation Protein Disorders; Factor VIII; Fibrinogen; Humans; Plasma; Rare Diseases

2016
Hereditary blood coagulation disorders: management and dental treatment.
    Journal of dental research, 2005, Volume: 84, Issue:11

    Topics: Blood Coagulation Disorders, Inherited; Coagulation Protein Disorders; Dental Care for Chronically Ill; Fibrinogen; Hemostasis; Humans; Thrombosis

2005
Gene targeting in hemostasis. tissue factor pathway inhibitor.
    Frontiers in bioscience : a journal and virtual library, 2001, Feb-01, Volume: 6

    Topics: Animals; Animals, Newborn; Coagulation Protein Disorders; Factor VII; Factor VII Deficiency; Fibrinogen; Gene Expression; Gene Targeting; Hemostasis; Humans; Kidney; Lipoproteins; Liver; Mice; Phenotype; Serine Proteinase Inhibitors

2001
Coagulation tests in differential diagnosis.
    Clinical and laboratory haematology, 2000, Volume: 22 Suppl 1

    Topics: Blood Coagulation Disorders; Blood Coagulation Tests; Coagulation Protein Disorders; Diagnosis, Differential; Fibrinogen; Humans; Platelet Function Tests; Specimen Handling; von Willebrand Diseases

2000
Personal practice: An approach to investigation of easy bruising.
    Archives of disease in childhood, 2001, Volume: 84, Issue:6

    Topics: Accidental Falls; Anti-Inflammatory Agents, Non-Steroidal; Child; Child Abuse; Child, Preschool; Coagulation Protein Disorders; Collagen Diseases; Contusions; Diagnosis, Differential; Fibrinogen; Humans; Infant; Infant, Newborn; Partial Thromboplastin Time; Platelet Aggregation Inhibitors; Prothrombin Time; Referral and Consultation; Thrombin Time; Thrombocytopenia; Vitamin K Deficiency Bleeding

2001

Trials

2 trial(s) available for fibrinogen and Blood Coagulation Factor Deficiencies

ArticleYear
Evaluation of the Q analyzer, a new cap-piercing fully automated coagulometer with clotting, chromogenic, and immunoturbidometric capability.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2013, Volume: 24, Issue:1

    Topics: Anticoagulants; Automation; Blood Coagulation; Blood Coagulation Disorders; Blood Coagulation Tests; Chromogenic Compounds; Coagulation Protein Disorders; Colorimetry; Drug Monitoring; Equipment Design; Fibrinogen; Heparin; High-Throughput Screening Assays; Humans; Indicators and Reagents; International Normalized Ratio; Nephelometry and Turbidimetry; Partial Thromboplastin Time; Reference Values; Reproducibility of Results; Sensitivity and Specificity; Warfarin

2013
[Randomised clinical trial of an intensive intervention into life-styles of patients with hyperfibrinogenaemia in primary prevention of cardiovascular pathology in primary health care].
    Atencion primaria, 2005, Mar-31, Volume: 35, Issue:5

    Topics: Adult; Aged; Cardiovascular Diseases; Coagulation Protein Disorders; Female; Fibrinogen; Humans; Life Style; Male; Middle Aged; Primary Health Care; Risk Factors

2005

Other Studies

19 other study(ies) available for fibrinogen and Blood Coagulation Factor Deficiencies

ArticleYear
The Clinical Efficacy of Fibrinogen Concentrate in Massive Obstetric Haemorrhage with Hypofibrinogenaemia.
    Scientific reports, 2017, Apr-24, Volume: 7

    Topics: Adult; Coagulation Protein Disorders; Female; Fibrinogen; Hemorrhage; Humans; Pregnancy; Pregnancy Complications; Retrospective Studies; Treatment Outcome; Young Adult

2017
Variability in international normalized ratio and activated partial thromboplastin time after injury are not explained by coagulation factor deficits.
    The journal of trauma and acute care surgery, 2019, Volume: 87, Issue:3

    Topics: Adolescent; Adult; Blood Coagulation Disorders; Blood Coagulation Factors; Case-Control Studies; Child; Coagulation Protein Disorders; Fibrinogen; Humans; International Normalized Ratio; Male; Partial Thromboplastin Time; Wounds and Injuries; Young Adult

2019
Preoperative plasma hyperfibrinogenemia is predictive of poor prognosis in patients with nonmetastatic colon cancer.
    Annals of surgical oncology, 2013, Volume: 20, Issue:9

    Topics: Biomarkers, Tumor; C-Reactive Protein; Carcinoembryonic Antigen; Coagulation Protein Disorders; Colonic Neoplasms; Female; Fibrinogen; Follow-Up Studies; Humans; Inflammation; Male; Middle Aged; Multivariate Analysis; Neoplasm Grading; Neoplasm Staging; Postoperative Complications; Preoperative Care; Prognosis; Retrospective Studies; Survival Rate

2013
Fibrinogen but not factor XIII deficiency is associated with bleeding after craniotomy.
    British journal of anaesthesia, 2014, Volume: 113, Issue:4

    Topics: Adolescent; Adult; Afibrinogenemia; Aged; Aged, 80 and over; Blood Coagulation Tests; Coagulation Protein Disorders; Confidence Intervals; Craniotomy; Factor XIII; Female; Fibrinogen; Humans; Male; Middle Aged; Neurosurgical Procedures; Odds Ratio; Partial Thromboplastin Time; Platelet Count; Postoperative Hemorrhage; Prospective Studies; ROC Curve; Young Adult

2014
Guideline for the diagnosis and management of the rare coagulation disorders: a United Kingdom Haemophilia Centre Doctors' Organization guideline on behalf of the British Committee for Standards in Haematology.
    British journal of haematology, 2014, Volume: 167, Issue:3

    Topics: Adult; Afibrinogenemia; Blood Coagulation Factors; Blood Coagulation Tests; Child; Coagulation Protein Disorders; Disease Management; Female; Fibrinogen; Hemorrhage; Hemorrhagic Disorders; Humans; Male; Pregnancy; Pregnancy Complications, Hematologic; Recombinant Proteins

2014
Why dysfibrinogenaemias still matter.
    Thrombosis and haemostasis, 2009, Volume: 102, Issue:3

    Topics: Blood Platelets; Coagulation Protein Disorders; Crystallography, X-Ray; Dimerization; Fibrin; Fibrinogen; Fibrinogens, Abnormal; Heterozygote; Humans; Models, Genetic; Mutation; Phosphorylation; Platelet Aggregation; Platelet Glycoprotein GPIIb-IIIa Complex; Protein Binding

2009
Two cases of congenital dysfibrinogenemia associated with thrombosis - Fibrinogen Praha III and Fibrinogen Plzen.
    Thrombosis and haemostasis, 2009, Volume: 102, Issue:3

    Topics: Adult; Blood Coagulation; Coagulation Protein Disorders; Female; Fibrin; Fibrinogen; Fibrinogens, Abnormal; Humans; Male; Microscopy, Electron, Scanning; Middle Aged; Mutation; Platelet Aggregation; Pulmonary Embolism; Thrombosis

2009
Oversulfated heparin by-products induce thrombin generation in human plasmas through contact system activation.
    Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis, 2010, Volume: 16, Issue:3

    Topics: Anaphylaxis; Anticoagulants; Blood Coagulation; Chondroitin Sulfates; Coagulation Protein Disorders; Disease Outbreaks; Drug Contamination; Enzyme Activation; Fibrinogen; Heparin; Humans; Kallikreins; Phosphatidylethanolamines; Prekallikrein; Prothrombin; Silicon Dioxide; Thrombin

2010
Hypofibrinogenemia caused by a nonsense mutation in the fibrinogen Bbeta chain gene.
    Journal of thrombosis and haemostasis : JTH, 2003, Volume: 1, Issue:11

    Topics: Aged; Coagulation Protein Disorders; Codon, Nonsense; Deoxyribonucleases, Type II Site-Specific; DNA Mutational Analysis; Female; Fibrinogen; Fibrinogens, Abnormal; Humans; Point Mutation

2003
Biophysical characterization of fibrinogen Caracas I with an Aalpha-chain truncation at Aalpha-466 Ser: identification of the mutation and biophysical characterization of properties of clots from plasma and purified fibrinogen.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2004, Volume: 15, Issue:4

    Topics: Biomechanical Phenomena; Blood Coagulation; Coagulation Protein Disorders; Codon, Nonsense; DNA Mutational Analysis; Family Health; Fibrin; Fibrinogen; Fibrinogens, Abnormal; Humans; Microscopy, Electron, Scanning; Porosity; Sequence Deletion

2004
Effects of coagulation factor deficiency on plasma coagulation kinetics determined via thrombelastography: critical roles of fibrinogen and factors II, VII, X and XII.
    Acta anaesthesiologica Scandinavica, 2005, Volume: 49, Issue:2

    Topics: Blood Coagulation; Blood Coagulation Factors; Coagulation Protein Disorders; Diatomaceous Earth; Dose-Response Relationship, Drug; Factor VII; Factor X; Factor XII; Fibrinogen; Humans; In Vitro Techniques; Kinetics; Plasma; Prothrombin; Thrombelastography; Thromboplastin

2005
A novel fibrinogen gamma chain mutation (gamma 239 Gln-->His) is the cause of dysfibrinogenemia Vicenza.
    Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:3

    Topics: Blood Coagulation Disorders, Inherited; Coagulation Protein Disorders; Fibrinogen; Fibrinogens, Abnormal; Humans; Mutation, Missense

2005
Study of coagulation factor activities in apheresed thawed fresh frozen plasma at 1-6 degrees C for five days.
    Journal of clinical apheresis, 2006, Volume: 21, Issue:4

    Topics: Adult; Blood Coagulation Factors; Blood Coagulation Tests; Blood Component Removal; Blood Preservation; Coagulation Protein Disorders; Cold Temperature; Fibrinogen; Humans; Plasma; Time Factors

2006
The fibrinogen Aalpha R16C mutation results in fibrinolytic resistance.
    British journal of haematology, 2006, Volume: 134, Issue:2

    Topics: Child, Preschool; Coagulation Protein Disorders; Fibrin; Fibrinogen; Fibrinogens, Abnormal; Fibrinolysis; Heterozygote; Humans; Male; Mutation

2006
Testing of platelet deposition on polystyrene surface under flow conditions by the cone and plate(let) analyzer: role of platelet activation, fibrinogen and von Willebrand factor.
    Thrombosis research, 2000, Aug-15, Volume: 99, Issue:4

    Topics: Afibrinogenemia; Coagulation Protein Disorders; Extracellular Matrix; Fibrinogen; Humans; Oligopeptides; Platelet Activation; Platelet Adhesiveness; Platelet Aggregation; Platelet Aggregation Inhibitors; Platelet Function Tests; Platelet Glycoprotein GPIIb-IIIa Complex; Polystyrenes; Solubility; Surface Properties; Thrombasthenia; von Willebrand Diseases; von Willebrand Factor

2000
Effect of citrate concentration on coagulation test results in dogs.
    Journal of the American Veterinary Medical Association, 2000, Dec-01, Volume: 217, Issue:11

    Topics: Animals; Anticoagulants; Citric Acid; Coagulation Protein Disorders; Dog Diseases; Dogs; Factor IX; Factor VIII; Fibrinogen; Hemophilia A; Hemophilia B; Partial Thromboplastin Time; Prothrombin Time; von Willebrand Diseases

2000
Inherited complete factor I deficiency associated with systemic lupus erythematosus, higher susceptibility to infection and low levels of factor H.
    Scandinavian journal of immunology, 2001, Volume: 53, Issue:6

    Topics: Adult; Bacterial Infections; Cell Migration Inhibition; Cells, Cultured; Child, Preschool; Coagulation Protein Disorders; Complement Activation; Complement C3; Complement C3b; Complement Factor H; Family Health; Female; Fibrinogen; Genetic Predisposition to Disease; Humans; Immunoelectrophoresis, Two-Dimensional; Lupus Erythematosus, Systemic; Phagocytosis

2001
Human plasma fibrinogen measurement derived from activated partial thromboplastin time clot formation.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2002, Volume: 13, Issue:1

    Topics: Adult; Aged; Anticoagulants; Blood Coagulation Tests; Coagulation Protein Disorders; Female; Fibrinogen; Humans; Immunoenzyme Techniques; Liver Diseases; Male; Middle Aged; Partial Thromboplastin Time; Predictive Value of Tests; Reproducibility of Results

2002
Studies of the human factor VIII/von Willebrand factor protein. III. Qualitative defects in von Willebrand's disease.
    The Journal of clinical investigation, 1975, Volume: 56, Issue:4

    Topics: Antibodies; Antigens; Blood Coagulation Tests; Chemical Precipitation; Chromatography, Gel; Chymotrypsin; Coagulation Protein Disorders; Counterimmunoelectrophoresis; Electrophoresis, Polyacrylamide Gel; Female; Fibrinogen; Hemophilia A; Humans; Male; Platelet Adhesiveness; Platelet Aggregation; Ristocetin; von Willebrand Diseases

1975