fibrinogen has been researched along with Inborn Errors of Metabolism in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (38.46) | 18.7374 |
| 1990's | 2 (15.38) | 18.2507 |
| 2000's | 4 (30.77) | 29.6817 |
| 2010's | 1 (7.69) | 24.3611 |
| 2020's | 1 (7.69) | 2.80 |
| Authors | Studies |
|---|---|
| Nishigami, T; Zen, Y | 1 |
| Pérez, B; Pérez-Cerdá, C; Richard, E; Roche, C; Ugarte, M; Vega, AI; Velázquez, R | 1 |
| Brennan, SO; Conard, K; Davis, RL; Furuya, KN; Savo, A | 1 |
| BURGSTEDT, HJ; MARX, R | 1 |
| Weisel, JW | 1 |
| Asselta, R; Braidotti, P; Coggi, G; Duga, S; Maggioni, M; Malcovati, M; Pellegrini, C; Santagostino, E; Tenchini, ML | 1 |
| Kawata, S; Mitsui, H; Miyahara, J; Miyauchi, E; Wada, K; Yamakawa, M | 1 |
| Branson, HE; Griffin, JH; Katz, J; Marble, R | 1 |
| De Craemer, D; Pipeleers-Marichal, M; van den Branden, C; Vandenplas, Y | 1 |
| Lukie, BE; Radhi, JM | 1 |
| Blombäck, M; Eriksson, AW; Lehmann, W; Nyman, D | 1 |
| Caringella, A; Rigillo, N; Spadaro, L; Torelli, M | 1 |
| Ratnoff, OD | 1 |
2 review(s) available for fibrinogen and Inborn Errors of Metabolism
| Article | Year |
|---|---|
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.
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.
Topics: Animals; Chemical Phenomena; Chemistry, Physical; Fibrin; Fibrinogen; Fibrinolysis; Humans; Metabolism, Inborn Errors; Protein Binding; Structure-Activity Relationship | 2005 |
11 other study(ies) available for fibrinogen and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Congenital disorder of glycosylation Ia: new differentially expressed proteins identified by 2-DE.
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.
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].
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
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.
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.
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.
Topics: Child; Female; Fibrinogen; Humans; Liver; Liver Diseases; Metabolism, Inborn Errors; Microbodies | 1996 |
Pancreatic cancer and fibrinogen storage disease.
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.
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].
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.
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 |