Page last updated: 2024-08-26

fibrinogen and Gasser Syndrome

fibrinogen has been researched along with Gasser Syndrome in 53 studies

Research

Studies (53)

TimeframeStudies, this research(%)All Research%
pre-199024 (45.28)18.7374
1990's2 (3.77)18.2507
2000's17 (32.08)29.6817
2010's10 (18.87)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Alberti, M; Bresin, E; Caprioli, J; Fremeaux-Bacchi, V; Goodship, TH; Noris, M; Pinto, S; Remuzzi, G; Ribes, D; Rodriguez de Cordoba, S; Rurali, E; Sanchez-Corral, P; Valoti, E1
Cervates, J; Dey, BR; Podder, S1
Alpers, CE; Fogo, AB; Lusco, MA; Najafian, B1
Larkin, K; Magun, BE; Melton-Celsa, AR; O'Brien, AD; Sauter, KA; Troxell, ML1
Bienaime, F; Blom, AM; Blouin, J; Dragon-Durey, MA; Fremeaux-Bacchi, V; Jablonski, M; Kwan, WH; Loirat, C; Nilsson, SC; Rameix-Welti, MA; Regnier, CH; Renault, N; Sautés-Fridman, C; Villoutreix, BO1
Huigen, M; Jansen, J; van de Kar, N; van den Heuvel, L; van der Heijden, E; van der Velden, T; van Kaauwen, E; Volokhina, E; Vos, A; Westra, D1
Noris, M; Remuzzi, G1
Garnier, A; Kwon, T; Loirat, C; Sellier-Leclerc, AL1
Ohsawa, I; Tomino, Y1
Dragon-Durey, MA; Fakhouri, F; Frémeaux-Bacchi, V; Loirat, C; Roumenina, L1
Bridoux, F; Cassuto, E; Chatelet, V; Delahousse, M; Frémeaux-Bacchi, V; Jablonski, M; Kamar, N; Le Quintrec, M; Lionet, A; Loirat, C; Moulin, B; Mourad, G; Mousson, C; Rondeau, E; Zuber, J1
Bermejo, E; Dran, GI; Fernández, GC; Gomez, S; Isturiz, MA; Meiss, R; Palermo, MS; Rubel, CJ1
de Córdoba, SR; Goicoechea, E; Huarte, O; López-Trascasa, M; Pérez-Caballero, D; Sánchez-Corral, P; Simckes, AM1
Fenwick, B; Friedman, KD; Raife, T1
Barrionuevo, P; Camerano, G; Dran, G; Fernández, GC; Gómez, SA; Isturiz, MA; Palermo, MS; Rosa, FA1
Ohi, H; Onda, K; Tomino, Y1
Caprioli, J; Peng, L; Remuzzi, G1
Licht, C; Misselwitz, J; Skerka, C; Zipfel, PF1
Goodship, TH; Kavanagh, D1
Faught, C; Kolajova, M; Rock, G; Zimmerman, D1
Blouin, J; Fakhouri, F; Frémeaux-Bacchi, V; Grünfeld, JP; Knebelmann, B; Lequintrec, M; Lesavre, P; Noël, LH; Salomon, R; Servais, A1
Loirat, C; Prüfer, F; Scheiring, J; Taylor, CM; Zimmerhackl, LB1
Abarrategui-Garrido, C; Frémeaux-Bacchi, V; Goicoechea de Jorge, E; Goodship, TH; López Trascasa, M; Noris, M; Perkins, SJ; Ponce Castro, IM; Remuzzi, G; Rodríguez de Córdoba, S; Sánchez-Corral, P; Saunders, RE; Skerka, C; Zipfel, PF1
Atkinson, JP; Burgess, R; Diaz-Torres, ML; Goodship, JA; Goodship, TH; Hourcade, DE; Kavanagh, D; Richards, A; Spitzer, D1
Alberti, C; Boudailliez, B; Bouissou, F; Deschenes, G; Dragon-Durey, MA; Fischbach, M; Fremeaux-Bacchi, V; Gie, S; Guest, G; Loirat, C; Macher, MA; Morin, D; Niaudet, P; Nivet, H; Sellier-Leclerc, AL; Tsimaratos, M1
Fukui, H; Iida, Y; Kamitsuji, H; Masuyama, H; Tani, K; Taniguchi, A1
Armas, JR; Fernández-Sanz, J; Galera, H; Matilla, A; Nogales, F1
Chang, AC; Dahlback, B; Esmon, CT; Hatanaka, K; Lockhart, MS; Peer, G; Taylor, FB1
Haycock, GB; Hunt, BJ; Jurd, KM; Lane, DA; Nevard, CH; Philippou, H1
Aihara, Y; Nakamura, T; Unayama, T; Yokota, S; Yoshida, Y1
Karpman, D; Lethagen, S; Mikaelsson, C; Nilsson, K; Papadopoulou, D; Sjögren, AC1
Anger, H1
Coopland, AT1
Kisker, CT; Rush, RA1
Arenson, EB; August, CS1
Hayslett, JP1
Abramowsky, CR; Krueger, R; McCoy, RC1
Ambrus, CM; Ambrus, JL; Baliah, T; Mink, IB; Murphy, GP1
Sutor, AH1
Denneberg, T; Ekberg, M; Nilsson, IM1
Brain, MC1
Hoyer, JR; Hoyer, LW; Michael, AF1
Breen, JL; Gregori, CA; Smith, H1
George, CR; Harker, LA; Quadracci, LJ; Slichter, SJ; Striker, GE1
Metz, J1
Harker, LA; Slichter, SJ1
Katz, J; Krawitz, S; Levin, J; Levin, SE; Metz, J; Sacks, PV; Thomson, P2
Clarkson, AR; Davison, AM; MacDonald, MK1
Stuart, J1
Barratt, TM; Chantler, C; Ekert, H; Turner, MW1
Murphy, AV; Willoughby, ML1
Jewell, FG; McMorris, S; Murphy, AV; Willoughby, ML1

Reviews

10 review(s) available for fibrinogen and Gasser Syndrome

ArticleYear
Plasmatherapy in atypical hemolytic uremic syndrome.
    Seminars in thrombosis and hemostasis, 2010, Volume: 36, Issue:6

    Topics: Complement Factor H; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Kidney Failure, Chronic; Membrane Cofactor Protein; Mutation; Plasma Exchange; Time Factors; Treatment Outcome

2010
[Immunologic tests: Properdin, factor H, factor I].
    Nihon rinsho. Japanese journal of clinical medicine, 2005, Volume: 63 Suppl 7

    Topics: Afibrinogenemia; Animals; Biomarkers; Complement Activation; Complement Factor H; Electrophoresis; Enzyme-Linked Immunosorbent Assay; Fibrinogen; Glomerulonephritis, Membranous; Hemolytic-Uremic Syndrome; Humans; Immunodiffusion; Immunologic Tests; Meningitis, Meningococcal; Nephelometry and Turbidimetry; Properdin; Reference Values

2005
The hemolytic uremic syndromes.
    Current opinion in critical care, 2005, Volume: 11, Issue:5

    Topics: Complement Factor H; Complement System Proteins; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Membrane Cofactor Protein; Mutation; Shiga Toxins

2005
The role of defective complement control in hemolytic uremic syndrome.
    Seminars in thrombosis and hemostasis, 2006, Volume: 32, Issue:2

    Topics: Complement Factor H; Complement Pathway, Alternative; Complement System Proteins; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Membrane Cofactor Protein; Models, Biological; Mutation

2006
Membrane cofactor protein and factor I: mutations and transplantation.
    Seminars in thrombosis and hemostasis, 2006, Volume: 32, Issue:2

    Topics: Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Kidney Transplantation; Membrane Cofactor Protein; Mutation

2006
Renal transplantation in HUS patients with disorders of complement regulation.
    Pediatric nephrology (Berlin, Germany), 2007, Volume: 22, Issue:1

    Topics: ADAM Proteins; ADAMTS13 Protein; Adolescent; Child; Child, Preschool; Complement Factor H; Europe; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Kidney Transplantation; Male; Neoplasm Recurrence, Local; Risk Factors; Treatment Outcome

2007
Current concepts. Postpartum renal failure.
    The New England journal of medicine, 1985, Jun-13, Volume: 312, Issue:24

    Topics: Acute Kidney Injury; Adult; Anemia, Hemolytic; Blood Coagulation Factors; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Hemostasis; Humans; Kidney; Platelet Aggregation; Pregnancy; Prognosis; Puerperal Disorders; Purpura, Thrombotic Thrombocytopenic; Thrombocytopenia; Thrombosis

1985
Fibrin-fibrinogen degradation products in children with renal disease.
    New York state journal of medicine, 1974, Volume: 74, Issue:8

    Topics: Acute Disease; Adolescent; Adult; Child; Child, Preschool; Chronic Disease; Female; Fibrin; Fibrinogen; Glomerulonephritis; Hemolytic-Uremic Syndrome; Humans; Immune Complex Diseases; Immunoglobulin A; Immunoglobulin G; Kidney Diseases; Lupus Erythematosus, Systemic; Male; Middle Aged; Nephritis; Nephrosis; Nephrotic Syndrome; Purpura; Streptococcal Infections

1974
Microangiopathic haemolytic anaemia (MHA).
    British journal of haematology, 1972, Volume: 23

    Topics: Adenocarcinoma; Anemia, Hemolytic; Animals; Blood Coagulation; Disseminated Intravascular Coagulation; Erythrocyte Aging; Erythrocytes, Abnormal; Fibrinogen; Hemolytic-Uremic Syndrome; Heparin; Humans; Hypertension, Malignant; Iodine Radioisotopes; Kidney Transplantation; Liver Transplantation; Purpura, Thrombotic Thrombocytopenic; Rabbits; Thromboplastin; Transplantation, Homologous; Venoms

1972
Disseminated intravascular coagulation in pregnancy.
    The Journal of the Medical Society of New Jersey, 1974, Volume: 71, Issue:10

    Topics: Abortion, Induced; Blood Coagulation; Blood Coagulation Tests; Disseminated Intravascular Coagulation; Female; Fibrinogen; Fibrinolysis; Hemolytic-Uremic Syndrome; Hemostasis; Humans; Hypotension; Pre-Eclampsia; Pregnancy; Pregnancy Complications, Hematologic; Prothrombin Time; Puerperal Disorders; Sodium Chloride

1974

Other Studies

43 other study(ies) available for fibrinogen and Gasser Syndrome

ArticleYear
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.
    Journal of the American Society of Nephrology : JASN, 2013, Volume: 24, Issue:3

    Topics: Adult; Atypical Hemolytic Uremic Syndrome; Child; Child, Preschool; Complement C3; Complement Factor B; Complement Factor H; Complement System Proteins; Female; Fibrinogen; Genetic Association Studies; Haplotypes; Hemolytic-Uremic Syndrome; Humans; Infant; Male; Membrane Cofactor Protein; Middle Aged; Mutation; Pedigree; Penetrance; Risk Factors; Young Adult

2013
Association of acquired thrombotic thrombocytopaenic purpura in a patient with pernicious anaemia.
    BMJ case reports, 2015, Oct-13, Volume: 2015

    Topics: ADAM Proteins; ADAMTS13 Protein; Aged; Anemia, Macrocytic; Anemia, Pernicious; Autoantibodies; Autoimmune Diseases; Erythrocyte Count; Erythrocytes, Abnormal; Erythropoiesis; Female; Fibrin Fibrinogen Degradation Products; Fibrinogen; Haptoglobins; Hemolytic-Uremic Syndrome; Humans; Intrinsic Factor; L-Lactate Dehydrogenase; Neutrophils; Purpura, Thrombotic Thrombocytopenic; Vitamin B 12

2015
AJKD Atlas of Renal Pathology: Thrombotic Microangiopathy.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2016, Volume: 68, Issue:6

    Topics: Complement C3; Fibrinogen; Glomerular Basement Membrane; Hemolytic-Uremic Syndrome; Humans; Immunoglobulin G; Immunoglobulin M; Kidney; Kidney Diseases; Microscopy; Microscopy, Electron; Microscopy, Fluorescence; Purpura, Thrombotic Thrombocytopenic; Thrombotic Microangiopathies

2016
Mouse model of hemolytic-uremic syndrome caused by endotoxin-free Shiga toxin 2 (Stx2) and protection from lethal outcome by anti-Stx2 antibody.
    Infection and immunity, 2008, Volume: 76, Issue:10

    Topics: Animals; Antibodies, Bacterial; Antibodies, Monoclonal; Antitoxins; Blood Urea Nitrogen; Child; Creatinine; Cytokines; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Immunohistochemistry; Kidney; Leukopenia; Mice; Mice, Inbred C57BL; Microscopy, Electron, Transmission; Proteinuria; Shiga Toxin 2

2008
Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome.
    Kidney international, 2010, Volume: 77, Issue:4

    Topics: Adolescent; Child; Child, Preschool; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Infant; Infant, Newborn; Male; Mutation; Young Adult

2010
Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS).
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2010, Volume: 25, Issue:7

    Topics: Adolescent; Adult; Autoantibodies; Case-Control Studies; Child; Child, Preschool; Complement Factor B; Complement Factor H; Complement System Proteins; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Infant; Male; Membrane Cofactor Protein; Middle Aged; Mutation; Netherlands; Polymorphism, Genetic; Young Adult

2010
Thrombotic microangiopathy after kidney transplantation.
    American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2010, Volume: 10, Issue:7

    Topics: Autoantibodies; Blood Component Transfusion; Child; Complement Factor H; Complement Pathway, Alternative; Complement System Proteins; Escherichia coli Infections; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Kidney Transplantation; Liver Transplantation; Mutation; Plasma; Postoperative Complications; Recurrence; Thrombotic Microangiopathies; Treatment Failure; Treatment Outcome

2010
[Properdin, factor H, factor I].
    Nihon rinsho. Japanese journal of clinical medicine, 2010, Volume: 68 Suppl 6

    Topics: Autoimmune Diseases; Biomarkers; Complement Activation; Complement Factor H; Enzyme-Linked Immunosorbent Assay; Fibrinogen; Glomerulonephritis, Membranoproliferative; Hemolytic-Uremic Syndrome; Humans; Immunodiffusion; Macular Degeneration; Nephelometry and Turbidimetry; Properdin; Reference Values; Specimen Handling

2010
[Atypical hemolytic-uremic syndrome related to abnormalities within the complement system].
    La Revue de medecine interne, 2011, Volume: 32, Issue:4

    Topics: Atypical Hemolytic Uremic Syndrome; Complement C3; Complement Factor B; Complement Factor H; Complement System Proteins; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Immunologic Factors; Membrane Cofactor Protein; Mutation; Plasma Exchange; Risk Factors; Treatment Outcome

2011
Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome.
    American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2013, Volume: 13, Issue:3

    Topics: Adolescent; Adult; Aged; Atypical Hemolytic Uremic Syndrome; Biomarkers; Complement C3; Complement Factor B; Complement Factor H; Complement System Proteins; Female; Fibrinogen; Genetic Testing; Graft Rejection; Graft Survival; Hemolytic-Uremic Syndrome; Humans; Kidney Transplantation; Male; Membrane Cofactor Protein; Middle Aged; Mutation; Prognosis; Recurrence; Retrospective Studies; Risk Factors; Young Adult

2013
Protective role of nitric oxide in mice with Shiga toxin-induced hemolytic uremic syndrome.
    Kidney international, 2002, Volume: 62, Issue:4

    Topics: Animals; Cell Degranulation; Enzyme Inhibitors; Fibrinogen; Hemolytic-Uremic Syndrome; Kidney Glomerulus; Mice; Mice, Inbred BALB C; NG-Nitroarginine Methyl Ester; Nitric Oxide; Platelet Activation; Shiga Toxin 2; Thrombosis; Urea

2002
Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome.
    American journal of human genetics, 2002, Volume: 71, Issue:6

    Topics: Animals; Base Sequence; Complement C3b; Complement Factor H; COS Cells; DNA Mutational Analysis; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Heterozygote; Humans; Male; Molecular Sequence Data; Molecular Weight; Mutation; Pedigree; Protein Binding

2002
Lepirudin prevents lethal effects of Shiga toxin in a canine model.
    Thrombosis and haemostasis, 2004, Volume: 92, Issue:2

    Topics: Animals; Anticoagulants; Blood Platelets; Cell-Free System; Coagulants; Dogs; Fibrinogen; Hemolytic-Uremic Syndrome; Hirudins; Kidney Glomerulus; Microscopy, Electron, Transmission; Partial Thromboplastin Time; Prothrombin; Prothrombin Time; Recombinant Proteins; Shiga Toxin 1; Shiga Toxin 2; Thrombin; Time Factors; von Willebrand Factor

2004
Endogenous glucocorticoids modulate neutrophil function in a murine model of haemolytic uraemic syndrome.
    Clinical and experimental immunology, 2005, Volume: 139, Issue:1

    Topics: Animals; Apoptosis; Cell Adhesion; Cell Migration Inhibition; Collagen Type II; Disease Models, Animal; Fibrinogen; Glucocorticoids; Hemolytic-Uremic Syndrome; Hormone Antagonists; Leukocyte Count; Male; Mice; Mice, Inbred BALB C; Mifepristone; Neutrophils; Phagocytosis; Reactive Oxygen Species; Receptors, Glucocorticoid; Serum Albumin, Bovine; Shiga Toxin 2; Tetradecanoylphorbol Acetate

2005
Identification of plasma antifibrin/fibrinogen antibodies in a patient with hemolytic uremic syndrome.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2006, Volume: 17, Issue:7

    Topics: ADAM Proteins; ADAMTS13 Protein; Adolescent; Antigen-Antibody Reactions; Autoantibodies; Blood Platelets; Female; Fibrin; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Immunoglobulin G; Platelet Aggregation; Recurrence; Renal Insufficiency; von Willebrand Factor

2006
Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.
    Journal of medical genetics, 2007, Volume: 44, Issue:3

    Topics: Adolescent; Adult; Aged; Child; Complement C3; Complement C3 Nephritic Factor; Complement Factor H; Complement Pathway, Alternative; Female; Fibrinogen; Genetic Predisposition to Disease; Glomerulonephritis; Glomerulonephritis, Membranoproliferative; Hemolytic-Uremic Syndrome; Humans; Male; Membrane Cofactor Protein; Mesangial Cells; Middle Aged; Retrospective Studies; Risk Factors

2007
The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models.
    Human mutation, 2007, Volume: 28, Issue:3

    Topics: Amino Acid Sequence; Complement Factor H; Databases, Genetic; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Membrane Cofactor Protein; Models, Molecular; Molecular Sequence Data; Mutation; Protein Structure, Tertiary; Sequence Homology, Amino Acid

2007
The decay accelerating factor mutation I197V found in hemolytic uraemic syndrome does not impair complement regulation.
    Molecular immunology, 2007, Volume: 44, Issue:12

    Topics: CD55 Antigens; Complement Factor H; Complement System Proteins; DNA Mutational Analysis; Family Health; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Membrane Cofactor Protein; Models, Molecular; Mutation; Mutation, Missense

2007
Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome.
    Journal of the American Society of Nephrology : JASN, 2007, Volume: 18, Issue:8

    Topics: Age of Onset; Child; Complement Factor H; Female; Fibrinogen; Genetic Predisposition to Disease; Hemolytic-Uremic Syndrome; Humans; Infant; Kidney Transplantation; Male; Membrane Cofactor Protein; Plasma; Point Mutation; Postoperative Complications; Prognosis; Risk Factors; Thrombosis; Treatment Outcome

2007
Urinary fibrin-fibrinogen degradation products and intraglomerular fibrin-fibrinogen deposition in various renal diseases.
    Thrombosis research, 1981, Feb-01, Volume: 21, Issue:3

    Topics: Child; Chromatography, Gel; Electrophoresis, Polyacrylamide Gel; Fibrin; Fibrin Fibrinogen Degradation Products; Fibrinogen; Glomerulonephritis; Hemolytic-Uremic Syndrome; Humans; Kidney Diseases; Kidney Glomerulus; Lupus Erythematosus, Systemic; Nephrotic Syndrome

1981
[Renal biopsy in the hemolytic-uremic syndrome in infancy. A study of three cases (author's transl)].
    Medicina clinica, 1980, Jan-25, Volume: 74, Issue:2

    Topics: Child, Preschool; Complement C3; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Immunoglobulins; Infant; Kidney; Male

1980
Role of free protein S and C4b binding protein in regulating the coagulant response to Escherichia coli.
    Blood, 1995, Oct-01, Volume: 86, Issue:7

    Topics: Animals; Blood Coagulation; Blood Platelets; Carrier Proteins; Complement Inactivator Proteins; Escherichia coli; Fibrinogen; Glycoproteins; Hematocrit; Hemolytic-Uremic Syndrome; Humans; Kidney Glomerulus; Mice; Mice, Inbred BALB C; Papio; Platelet Count; Protein S

1995
Activation of coagulation and fibrinolysis in childhood diarrhoea-associated haemolytic uraemic syndrome.
    Thrombosis and haemostasis, 1997, Volume: 78, Issue:6

    Topics: Antithrombin III; Blood Coagulation; Blood Transfusion; Child; Diarrhea; Factor VIIa; Factor XIIa; Fibrin; Fibrin Fibrinogen Degradation Products; Fibrinogen; Fibrinolysis; Hemolytic-Uremic Syndrome; Humans; Peptide Fragments; Peritoneal Dialysis; Plasma Exchange; Plasminogen Activator Inhibitor 1; Prothrombin; Renal Dialysis; Thrombin; Tissue Plasminogen Activator

1997
Usefulness of serum fibrinogen degradation product-E in sporadic cases of classical hemolytic uremic syndrome.
    Pediatrics international : official journal of the Japan Pediatric Society, 2000, Volume: 42, Issue:5

    Topics: Biomarkers; Child; Child, Preschool; Escherichia coli Infections; Escherichia coli O157; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Male; Predictive Value of Tests; Prognosis; Retrospective Studies; Severity of Illness Index

2000
Platelet activation by Shiga toxin and circulatory factors as a pathogenetic mechanism in the hemolytic uremic syndrome.
    Blood, 2001, May-15, Volume: 97, Issue:10

    Topics: Adolescent; Blood Platelets; Child; Child, Preschool; Endothelium, Vascular; Escherichia coli; Escherichia coli Infections; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Infant; Male; Platelet Activation; Shiga Toxin; Shiga Toxin 1; Shiga Toxin 2; Tumor Necrosis Factor-alpha; Umbilical Veins

2001
[Fibrin (ogen) Split products of nephropathies].
    Der Urologe. Ausg. A, 1975, Volume: 14, Issue:1

    Topics: Disseminated Intravascular Coagulation; Female; Fibrin; Fibrinogen; Fibrinolysis; Glomerulonephritis; Graft vs Host Reaction; Hemolytic-Uremic Syndrome; Humans; Immunoelectrophoresis; Infant; Kidney Diseases; Kidney Transplantation; Molecular Weight; Pre-Eclampsia; Pregnancy; Prognosis; Thrombosis; Transplantation, Homologous; Urinary Tract Infections

1975
A case of haemolytic-uraemic syndrome.
    British medical journal, 1979, Sep-15, Volume: 2, Issue:6191

    Topics: Female; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Pregnancy; Pregnancy Complications, Hematologic

1979
Absence of intravascular coagulation in the hemolytic-uremic syndrome.
    American journal of diseases of children (1960), 1975, Volume: 129, Issue:2

    Topics: Anuria; Blood Cell Count; Blood Coagulation Tests; Blood Platelets; Blood Pressure; Blood Urea Nitrogen; Carbon Radioisotopes; Child; Child, Preschool; Creatinine; Disseminated Intravascular Coagulation; Factor V; Factor VIII; Female; Fibrin; Fibrinogen; Hematuria; Hemoglobins; Hemolytic-Uremic Syndrome; Heparin; Humans; Infant; Male; Proteinuria; Prothrombin Time; Thromboplastin; Thrombosis

1975
Preliminary report: treatment of the hemolytic-uremic syndrome with aspirin and dipyridamole.
    The Journal of pediatrics, 1975, Volume: 86, Issue:6

    Topics: Acute Disease; Anemia, Hemolytic; Aspirin; Blood Platelet Disorders; Blood Platelets; Blood Transfusion; Child; Child, Preschool; Dipyridamole; Diuresis; Dose-Response Relationship, Drug; Drug Administration Schedule; Erythrocyte Aggregation; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Heparin; Humans; Infant; Kidney Diseases; Male; Platelet Adhesiveness; Remission, Spontaneous; Thrombocytopenia

1975
The hemolytic uremic syndrome, with positive immunofluorescence studies.
    The Journal of pediatrics, 1974, Volume: 85, Issue:2

    Topics: Arteries; Autopsy; Beta-Globulins; Biopsy; Female; Fibrinogen; Fluorescent Antibody Technique; Hemolytic-Uremic Syndrome; Humans; Immunity; Immunoglobulin M; Immunoglobulins; Infant; Infant, Newborn; Kidney; Kidney Cortex; Kidney Glomerulus; Skin

1974
[The heat lysis time, a new in vivo method for the determination of hemostasis].
    Blut, 1974, Volume: 29, Issue:3

    Topics: Blood Cell Count; Blood Coagulation; Blood Coagulation Tests; Blood Platelets; Capillary Resistance; Child; Factor VIII; Fibrinogen; Hemolytic-Uremic Syndrome; Hemophilia A; Heparin; Hot Temperature; Humans; In Vitro Techniques; Infant; Kidney Failure, Chronic; Male; Nephrotic Syndrome; Plasminogen; Platelet Adhesiveness; Platelet Aggregation; Prothrombin Time; Serum Globulins; Thromboplastin

1974
Coagulation studies in hemolytic uremic syndrome and thrombotic thrombocytopenic purpura.
    Acta medica Scandinavica, 1974, Volume: 196, Issue:5

    Topics: Adult; Blood Coagulation Tests; Blood Platelets; Child, Preschool; Chromium Radioisotopes; Creatinine; Factor V; Factor VIII; Factor XIII; Female; Fibrin; Fibrinogen; Fibrinolysis; Haptoglobins; Hematocrit; Hemolytic-Uremic Syndrome; Humans; Infant; Male; Middle Aged; Plasminogen; Prothrombin; Purpura, Thrombotic Thrombocytopenic; Thrombin

1974
Immunofluorescent localization of antihemophilic factor antigen and fibrinogen in human renal diseases.
    The Journal of clinical investigation, 1974, Volume: 53, Issue:5

    Topics: Arteries; Biopsy; Capillaries; Factor VIII; Fibrinogen; Glomerulonephritis; Hemolytic-Uremic Syndrome; Humans; Hypertension, Malignant; Kidney; Kidney Diseases; Kidney Glomerulus; Kidney Transplantation; Microscopy, Fluorescence; Purpura; Scleroderma, Systemic; Transplantation, Homologous; Veins

1974
A kinetic evaluation of hemostasis in renal disease.
    The New England journal of medicine, 1974, Nov-21, Volume: 291, Issue:21

    Topics: Aspirin; Blood Coagulation; Complement System Proteins; Diabetic Nephropathies; Dipyridamole; Fibrin; Fibrinogen; Glomerulonephritis; Hemolytic-Uremic Syndrome; Heparin; Humans; Iodine Radioisotopes; Kidney; Kidney Diseases; Kidney Glomerulus; Kidney Transplantation; Plasminogen; Proteinuria; Thrombosis; Transplantation, Homologous; Uremia; Warfarin

1974
Observations on the mechanism of the haematological changes in the haemolytic uraemic syndrome of infancy.
    British journal of haematology, 1972, Volume: 23

    Topics: Acute Kidney Injury; Anemia, Hemolytic; Blood Coagulation; Blood Platelets; Disseminated Intravascular Coagulation; Erythrocyte Aging; Fibrinogen; Fibrinolytic Agents; Hemolytic-Uremic Syndrome; Heparin; Humans; Infant; Iodine Isotopes; Thrombocytopenia; Uremia

1972
Platelet and fibrinogen consumption in man.
    The New England journal of medicine, 1972, Nov-16, Volume: 287, Issue:20

    Topics: Blood Cell Count; Blood Platelets; Catheterization; Cell Survival; Dipyridamole; Disseminated Intravascular Coagulation; Female; Fibrinogen; Fibrinolytic Agents; Heart Valve Prosthesis; Hemolytic-Uremic Syndrome; Heparin; Humans; Inflammation; Neoplasms; Postoperative Complications; Purpura, Thrombotic Thrombocytopenic; Sepsis; Surgical Procedures, Operative; Thromboembolism; Thrombophlebitis; Thrombosis; Vascular Diseases

1972
Platelet, erythrocyte, and fibrinogen kinetics in the hemolytic-uremic syndrome of infancy.
    The Journal of pediatrics, 1973, Volume: 83, Issue:5

    Topics: Abdomen; Anemia; Blood Platelets; Blood Urea Nitrogen; Chromium Radioisotopes; Erythrocytes; Fibrinogen; Haptoglobins; Hemoglobins; Hemolytic-Uremic Syndrome; Humans; Infant; Iodine Radioisotopes; Kidney; Kinetics; Liver; Radionuclide Imaging; Spleen; Time Factors

1973
The role of coagulation in renal disease.
    Perspectives in nephrology and hypertension, 1973, Volume: 1 Pt 2, Issue:0

    Topics: Acute Kidney Injury; Basement Membrane; Blood Coagulation Disorders; Diabetic Nephropathies; Disseminated Intravascular Coagulation; Female; Fibrin; Fibrinogen; Fibrinolysis; Glomerulonephritis; Hemagglutination Tests; Hemolytic-Uremic Syndrome; Humans; Ischemia; Kidney; Kidney Diseases; Male; Middle Aged; Pre-Eclampsia; Pregnancy; Thrombosis; Urokinase-Type Plasminogen Activator

1973
Excess intravascular coagulation--diagnosis and clinical significance.
    Proceedings of the Royal Society of Medicine, 1974, Volume: 67, Issue:3

    Topics: Blood Coagulation Tests; Child; Child, Preschool; Disseminated Intravascular Coagulation; Factor V; Factor VIII; Fibrin; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Infant; Prothrombin Time; Sepsis

1974
Immunologically reactive equivalents of fibrinogen in sera and urine of children with renal disease.
    Archives of disease in childhood, 1972, Volume: 47, Issue:251

    Topics: Adolescent; Albuminuria; Antigens; Child; Child, Preschool; Fanconi Syndrome; Fibrinogen; Glomerulonephritis; Hemagglutination Inhibition Tests; Hematuria; Hemolytic-Uremic Syndrome; Humans; Infant; Kidney Diseases; Kidney Glomerulus; Nephrotic Syndrome; Proteinuria

1972
Coagulation studies in the haemolytic uraemic syndrome.
    Archives of disease in childhood, 1972, Volume: 47, Issue:252

    Topics: Anemia, Hemolytic; Blood Coagulation; Blood Coagulation Factors; Blood Platelets; Fibrin; Fibrinogen; Hemolytic-Uremic Syndrome; Heparin; Humans; Uremia

1972
Radio-isotopic studies of erythrocytes, platelets and fibrinogen in the haemolytic-uraemic syndrome of infancy.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1972, Jun-17, Volume: 46, Issue:25

    Topics: Anemia, Hemolytic; Blood Platelets; Chromium Isotopes; Erythrocyte Aging; Erythrocytes; Fibrinogen; Half-Life; Hemolytic-Uremic Syndrome; Humans; Infant; Time Factors; Uremia

1972
Coagulation studies in haemolytic uraemic syndrome.
    Archives of disease in childhood, 1972, Volume: 47, Issue:255

    Topics: Anemia, Hemolytic; Blood Cell Count; Blood Coagulation; Blood Platelets; Child; Disseminated Intravascular Coagulation; Factor V; Factor VIII; Female; Fibrinogen; Hemolytic-Uremic Syndrome; Heparin; Humans; Infant; Male; Plasminogen; Uremia; Urine

1972