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fibrinogen and Metabolism, Inborn Errors

fibrinogen has been researched along with Metabolism, Inborn Errors in 13 studies

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19905 (38.46)18.7374
1990's2 (15.38)18.2507
2000's4 (30.77)29.6817
2010's1 (7.69)24.3611
2020's1 (7.69)2.80

Authors

AuthorsStudies
Nishigami, T; Zen, Y1
Pérez, B; Pérez-Cerdá, C; Richard, E; Roche, C; Ugarte, M; Vega, AI; Velázquez, R1
Brennan, SO; Conard, K; Davis, RL; Furuya, KN; Savo, A1
BURGSTEDT, HJ; MARX, R1
Weisel, JW1
Asselta, R; Braidotti, P; Coggi, G; Duga, S; Maggioni, M; Malcovati, M; Pellegrini, C; Santagostino, E; Tenchini, ML1
Kawata, S; Mitsui, H; Miyahara, J; Miyauchi, E; Wada, K; Yamakawa, M1
Branson, HE; Griffin, JH; Katz, J; Marble, R1
De Craemer, D; Pipeleers-Marichal, M; van den Branden, C; Vandenplas, Y1
Lukie, BE; Radhi, JM1
Blombäck, M; Eriksson, AW; Lehmann, W; Nyman, D1
Caringella, A; Rigillo, N; Spadaro, L; Torelli, M1
Ratnoff, OD1

Reviews

2 review(s) available for fibrinogen and Metabolism, Inborn Errors

ArticleYear
Rethinking fibrinogen storage disease of the liver: ground glass and globular inclusions do not represent a congenital metabolic disorder but acquired collective retention of proteins.
    Human pathology, 2020, Volume: 100

    Topics: Adult; Biomarkers; Biopsy; C-Reactive Protein; Complement C4b; Female; Fibrinogen; Humans; Immunohistochemistry; Inclusion Bodies; Liver; Liver Diseases; Male; Metabolism, Inborn Errors; Middle Aged; Peptide Fragments; Terminology as Topic

2020
Fibrinogen and fibrin.
    Advances in protein chemistry, 2005, Volume: 70

    Topics: Animals; Chemical Phenomena; Chemistry, Physical; Fibrin; Fibrinogen; Fibrinolysis; Humans; Metabolism, Inborn Errors; Protein Binding; Structure-Activity Relationship

2005

Other Studies

11 other study(ies) available for fibrinogen and Metabolism, Inborn Errors

ArticleYear
Congenital disorder of glycosylation Ia: new differentially expressed proteins identified by 2-DE.
    Biochemical and biophysical research communications, 2009, Feb-06, Volume: 379, Issue:2

    Topics: alpha 1-Antitrypsin; alpha-Macroglobulins; Carrier Proteins; Child; Child, Preschool; Electrophoresis, Gel, Two-Dimensional; Female; Fibrin; Fibrinogen; Glycoproteins; Glycosylation; Humans; Isoelectric Focusing; Metabolism, Inborn Errors; Protein Biosynthesis; Proteins; Proteome; Proteomics; Serum; Serum Albumin; Serum Albumin, Human; Transferrin

2009
Novel fibrinogen mutation γ314Thr→Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia.
    Liver international : official journal of the International Association for the Study of the Liver, 2010, Volume: 30, Issue:10

    Topics: Afibrinogenemia; Alanine Transaminase; Aspartate Aminotransferases; Biomarkers; Blood Coagulation; Child, Preschool; Chromatography, High Pressure Liquid; Chromatography, Reverse-Phase; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Fibrinogen; Genetic Predisposition to Disease; Humans; Inclusion Bodies; International Normalized Ratio; Liver; Liver Diseases; Male; Metabolism, Inborn Errors; Models, Molecular; Mutation; Phenotype; Protein Conformation; Structure-Activity Relationship

2010
[Afibrinogenemia, parahemophilic syndrome and dysproteinemia in cystine storage disorders as an indication to the pathogenesis of the disease].
    Klinische Wochenschrift, 1956, Jan-01, Volume: 34, Issue:1-2

    Topics: Afibrinogenemia; Blood Protein Disorders; Blood Proteins; Cystine; Female; Fibrinogen; Hemorrhagic Disorders; Humans; Metabolism, Inborn Errors; Pregnancy

1956
Liver histology of an afibrinogenemic patient with the Bbeta-L353R mutation showing no evidence of hepatic endoplasmic reticulum storage disease (ERSD); comparative study in COS-1 cells of the intracellular processing of the Bbeta-L353R fibrinogen vs. the
    Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:4

    Topics: Adolescent; Animals; Arginine; COS Cells; DNA, Complementary; Electrophoresis, Polyacrylamide Gel; Endoplasmic Reticulum; Fibrinogen; Genotype; Glycoside Hydrolases; Humans; Immunohistochemistry; Immunoprecipitation; Leucine; Liver; Liver Diseases; Male; Metabolism, Inborn Errors; Microscopy, Electron; Mutation; Mutation, Missense; Phenotype; Reverse Transcriptase Polymerase Chain Reaction; RNA; RNA, Messenger; Transfection

2005
A case of primary biliary cirrhosis accompanied with fibrinogen storage disease.
    Pathology, research and practice, 2005, Volume: 201, Issue:4

    Topics: Alkaline Phosphatase; Autoantibodies; Biomarkers; Female; Fibrinogen; gamma-Glutamyltransferase; Hepatocytes; HSP70 Heat-Shock Proteins; Humans; Immunoenzyme Techniques; Inclusion Bodies; Liver Cirrhosis, Biliary; Metabolism, Inborn Errors; Middle Aged; Mitochondria; Ubiquitin

2005
Inherited protein C deficiency and coumarin-responsive chronic relapsing purpura fulminans in a newborn infant.
    Lancet (London, England), 1983, Nov-19, Volume: 2, Issue:8360

    Topics: Child; Chronic Disease; Coumarins; Disseminated Intravascular Coagulation; Fibrinogen; Gangrene; Glycoproteins; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Pedigree; Protein C; Purpura; Skin; Syndrome

1983
Peroxisome proliferation associated with fibrinogen storage in the liver.
    Histopathology, 1996, Volume: 29, Issue:2

    Topics: Child; Female; Fibrinogen; Humans; Liver; Liver Diseases; Metabolism, Inborn Errors; Microbodies

1996
Pancreatic cancer and fibrinogen storage disease.
    Journal of clinical pathology, 1998, Volume: 51, Issue:11

    Topics: Adenocarcinoma; Adult; Aged; Fatal Outcome; Fibrinogen; Humans; Male; Metabolism, Inborn Errors; Pancreatic Neoplasms; Pedigree

1998
Inherited defective platelet aggregation with arachidonate as the main expression of a defective metabolism of arachidonic acid.
    Thrombosis research, 1979, Volume: 14, Issue:4-5

    Topics: Adenosine Diphosphate; Adolescent; Adult; Aged; Arachidonic Acids; Bleeding Time; Blood Platelet Disorders; Child; Child, Preschool; Female; Fibrinogen; Humans; Male; Metabolism, Inborn Errors; Middle Aged; Pedigree; Platelet Aggregation; Thromboplastin

1979
[Determination of haptoglobin, Winzler's orosomucoid, plasmatic fibrinogen and urinary acid mucopolysaccharides in Marfan's syndrome].
    La Pediatria, 1969, Volume: 77, Issue:3

    Topics: Adolescent; Child; Connective Tissue; Fibrinogen; Glycoproteins; Glycosaminoglycans; Haptoglobins; Humans; Male; Marfan Syndrome; Metabolism, Inborn Errors

1969
Hereditary disorders of blood coagulation. Deficient synthesis versus defective synthesis.
    Journal of chronic diseases, 1971, Volume: 24, Issue:2

    Topics: Afibrinogenemia; Blood Coagulation Disorders; Blood Coagulation Factors; Factor IX; Factor VIII; Fibrinogen; Hemophilia A; Hemophilia B; Humans; Hypoprothrombinemias; Metabolism, Inborn Errors; Prothrombin; von Willebrand Diseases

1971