tyrosine has been researched along with Coagulation Disorders, Blood in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (66.67) | 18.7374 |
| 1990's | 3 (25.00) | 18.2507 |
| 2000's | 1 (8.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bratkovic, D; Couper, R; Davidson, GP; Fahy, R; Fletcher, JM; Mackay, RJ; Ranieri, E | 1 |
| Ficici, S; Fraser, D; Jackson, SH; Kooh, SW; Paunier, L; Sass-Kortsak, A | 1 |
| Evans, DI; Sardharwalla, IB | 1 |
| Bharadwaj, D; Foster, DC; Iino, M; Kisiel, W; Kontoyianni, M; Smith, KJ | 1 |
| Chong, SK; Croffie, JM; Fitzgerald, JF; Gupta, SK | 1 |
| Dachary-Prigent, J; Fressinaud, E; Freyssinet, JM; Martin, S; MartÃnez, MC; Meyer, D; Toti, F | 1 |
| Vinazzer, H | 1 |
| Beaufils, F; Bourrillon, A; Mercier, JC; Odievre, M | 1 |
| Ozsoylu, S | 1 |
| Derleth, TR; Penner, JA | 1 |
| Stenflo, J | 1 |
| Bengmark, S; Hafstrom, LO; Korsan-Bengtsen, K | 1 |
12 other study(ies) available for tyrosine and Coagulation Disorders, Blood
| Article | Year |
|---|---|
Detection of treatable neonatal liver disease by expanded newborn screening.
Topics: alpha-Fetoproteins; Amino Acid Metabolism, Inborn Errors; Antioxidants; Biomarkers; Blood Coagulation Disorders; Diagnosis, Differential; Ferritins; Hemochromatosis; Humans; Hypoalbuminemia; Infant, Newborn; Iron; Iron Chelating Agents; Liver; Male; Methionine; Neonatal Screening; Predictive Value of Tests; Tandem Mass Spectrometry; Treatment Outcome; Tyrosine | 2008 |
Secondary metabolic derangements in patients with tyrosyluria.
Topics: Amino Acid Metabolism, Inborn Errors; Blood Coagulation Disorders; Blood Protein Disorders; Carbohydrate Metabolism; Copper; Humans; Infant; Tyrosine | 1967 |
Coagulation defect of congenital tyrosinaemia.
Topics: Afibrinogenemia; Amino Acid Metabolism, Inborn Errors; Blood Coagulation Disorders; Blood Coagulation Factors; Female; Humans; Infant, Newborn; Liver; Male; Tyrosine | 1984 |
Factor VII central. A novel mutation in the catalytic domain that reduces tissue factor binding, impairs activation by factor Xa, and abolishes amidolytic and coagulant activity.
Topics: Adult; Aspartic Acid; Blood Coagulation Disorders; Factor VII; Factor Xa; Humans; Hydrogen Bonding; Male; Models, Molecular; Point Mutation; Recombinant Proteins; Structure-Activity Relationship; Thromboplastin; Tyrosine | 1996 |
Tyrosinemia type 1 should be suspected in infants with severe coagulopathy even in the absence of other signs of liver failure.
Topics: Amino Acid Metabolism, Inborn Errors; Blood Coagulation Disorders; Female; Humans; Infant; Liver Failure; Liver Transplantation; Male; Tyrosine | 1999 |
Significance of capacitative Ca2+ entry in the regulation of phosphatidylserine expression at the surface of stimulated cells.
Topics: Aged; B-Lymphocytes; Blood Coagulation Disorders; Calcimycin; Calcium Channels; Cell Membrane; Cell Transformation, Viral; Cells, Cultured; Enzyme Inhibitors; Female; Genistein; Humans; Lymphocyte Activation; Phosphatidylserines; Phospholipids; Phosphorylation; Protein-Tyrosine Kinases; Syndrome; Thapsigargin; Tyrosine | 1999 |
Coagulation studies during therapeutic application of arvin.
Topics: Afibrinogenemia; Ancrod; Batroxobin; Blood Coagulation; Blood Coagulation Disorders; Blood Platelet Disorders; Blood Platelets; Drug Resistance; Endopeptidases; Fibrinogen; Fibrinolysis; Humans; Injections, Intravenous; Injections, Subcutaneous; Platelet Aggregation; Thrombin; Thrombocytopenia; Tyrosine | 1976 |
[Hereditary fructose intolerance with early onset].
Topics: Alanine Transaminase; Blood Coagulation Disorders; Carbohydrate Metabolism, Inborn Errors; Diagnosis, Differential; Exchange Transfusion, Whole Blood; Female; Fructose Intolerance; Fructose-Bisphosphate Aldolase; Galactosemias; Hemorrhage; Hepatomegaly; Humans; Hypoglycemia; Infant; Infant, Newborn; Jaundice; Liver; Liver Function Tests; Neurologic Manifestations; Prognosis; Respiratory Insufficiency; Tyrosine | 1976 |
Coagulation defect of congenital tyrosinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Blood Coagulation Disorders; Child, Preschool; Humans; Male; Tyrosine | 1985 |
Human prothrombin. Chromatographic separation from normal and deficient plasmas.
Topics: Alpha-Globulins; Blood Coagulation Disorders; Blood Coagulation Factors; Blood Coagulation Tests; Blood Glucose; Blood Protein Electrophoresis; Blood Proteins; Chromatography; Chromatography, DEAE-Cellulose; Hexosamines; Humans; Immunoelectrophoresis; Neuraminic Acids; Prothrombin; Prothrombin Time; Spectrophotometry; Tyrosine; Ultracentrifugation | 1970 |
Vitamin K and the biosynthesis of prothrombin. II. Structural comparison of normal and dicoumarol-induced bovine prothrombin.
Topics: Alkylation; Amino Acids; Animals; Blood Coagulation Disorders; Calcium; Carbohydrates; Cattle; Chemical Phenomena; Chemistry; Cyanogen Bromide; Dicumarol; Electrophoresis, Polyacrylamide Gel; Epitopes; Immunodiffusion; Isoelectric Focusing; Molecular Weight; Peptides; Protein Binding; Protein Conformation; Prothrombin; Spectrometry, Fluorescence; Spectrophotometry, Ultraviolet; Sulfhydryl Compounds; Tyrosine; Ultracentrifugation; Vitamin K | 1972 |
Effects on blood clotting and circulation of autologous connective tissue homogenate infusion in dogs.
Topics: Animals; Bicarbonates; Blood Circulation; Blood Coagulation Disorders; Blood Coagulation Tests; Blood Platelets; Blood Pressure; Carbon Dioxide; Collagen; Connective Tissue; Dogs; Erythrocyte Count; Factor V; Factor VII; Factor VIII; Factor X; Fibrinogen; Hematocrit; Hemoglobinometry; Hydrogen-Ion Concentration; Infusions, Parenteral; Plasminogen; Proteins; Prothrombin; Tyrosine | 1969 |