tyrosine has been researched along with Hepatic Failure in 16 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 8 (50.00) | 18.2507 |
2000's | 5 (31.25) | 29.6817 |
2010's | 3 (18.75) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Morrow, G; Tanguay, RM | 1 |
Qi, Z; Sun, R; Tian, Z; Wang, X; Wei, H | 1 |
Chinault, AC; Dimmock, D; Huang, WC; Hwu, WL; Lee, NC; Tang, LY; Wong, LJ | 1 |
Jitraruch, S; Leelaudomlipi, S; Sornmayura, P; Sriphojanart, S; Teeraratkul, S; Treepongkaruna, S; Viengteerawat, S; Wattanasirichaigoon, D | 1 |
McKiernan, PJ | 1 |
Aregullin, M; Lei, XG; McClung, JP; Roneker, CA; Zhu, JH | 1 |
Dejong, CH; Jalan, R; Olde Damink, SW; Soeters, PB; van de Poll, MC | 1 |
Druml, W; Hoerauf, K; Krenn, CG; Pokorny, H; Roth, E; Stark, J; Steltzer, H | 1 |
de la Vega, A; Diaz, MC; Gamez, M; Jara, P; Lopez Santamaria, M; Murcia, FJ; Tovar, J; Vazquez, J | 1 |
Druml, W; Hübl, W; Lochs, H; Roth, E | 1 |
Bensoussan, AL; Blanchard, H; Bruneau, N; LaBerge, JM; Luks, FI; St-Vil, D | 1 |
Kane, PA; Karani, JB; Meili-Vergani, G; Williams, R | 1 |
Berger, R; Mustonen, A; Ploos van Amstel, HK; Salo, MK; Simola, KO; Viinikka, L | 1 |
Chong, SK; Croffie, JM; Fitzgerald, JF; Gupta, SK | 1 |
Barkaoui, E; Bernard, O; Debray, D; Habès, D; Ogier, H | 1 |
Kelsey, G; Ruppert, S; Schedl, A; Schmid, E; Schütz, G; Thies, E | 1 |
3 review(s) available for tyrosine and Hepatic Failure
Article | Year |
---|---|
Biochemical and Clinical Aspects of Hereditary Tyrosinemia Type 1.
Topics: Cyclohexanones; Humans; Kidney; Liver; Liver Failure; Nitrobenzoates; Tyrosine; Tyrosinemias | 2017 |
Aromatic amino acid metabolism during liver failure.
Topics: Amino Acids, Aromatic; Ammonia; Biological Transport; Humans; Liver Failure; Phenylalanine; Reference Values; Tryptophan; Tyrosine | 2007 |
Multiple effects on liver-specific gene expression in albino lethal mice caused by deficiency of an enzyme in tyrosine metabolism.
Topics: Animals; Gene Expression Regulation; Genes, Lethal; Hydrolases; Liver; Liver Failure; Mice; Phenotype; Tyrosine | 1992 |
1 trial(s) available for tyrosine and Hepatic Failure
Article | Year |
---|---|
Utilization of tyrosine-containing dipeptides and N-acetyl-tyrosine in hepatic failure.
Topics: Adult; Aged; Dipeptides; Female; Half-Life; Humans; Liver Failure; Male; Metabolic Clearance Rate; Middle Aged; Tyrosine | 1995 |
12 other study(ies) available for tyrosine and Hepatic Failure
Article | Year |
---|---|
Infiltrating neutrophils aggravate metabolic liver failure in fah-deficient mice.
Topics: Animals; Bilirubin; Body Weight; Cyclohexanones; Disease Models, Animal; Hepatocytes; Hydrolases; Inflammation; Interleukin-22; Interleukins; Liver; Liver Failure; Male; Mice; Mice, Knockout; Neutrophils; Nitrobenzoates; Receptors, CCR2; Tyrosine | 2015 |
Simultaneous detection of mitochondrial DNA depletion and single-exon deletion in the deoxyguanosine gene using array-based comparative genomic hybridisation.
Topics: Alanine; Base Sequence; Deoxyguanine Nucleotides; DNA Mutational Analysis; DNA, Mitochondrial; Exons; Gene Deletion; Genetic Carrier Screening; Humans; Infant; Infant, Newborn; Liver Failure; Male; Mitochondrial Diseases; Molecular Sequence Data; Mutation, Missense; Oligonucleotide Array Sequence Analysis; Tandem Mass Spectrometry; Treatment Outcome; Tyrosine | 2009 |
Long-term outcome of living donor liver transplantation in a Thai boy with hereditary tyrosinemia type I: a case report.
Topics: Asian People; Diet Therapy; Heptanoates; Humans; Hydrolases; Infant; Liver Failure; Liver Transplantation; Living Donors; Male; Mutation; Phenylalanine; Thailand; Treatment Outcome; Tyrosine; Tyrosinemias | 2011 |
Nitisinone in the treatment of hereditary tyrosinaemia type 1.
Topics: Carcinoma, Hepatocellular; Cyclohexanones; Enzyme Inhibitors; Humans; Kidney Diseases; Liver Diseases; Liver Failure; Liver Neoplasms; Liver Transplantation; Monitoring, Physiologic; Nitrobenzoates; Tyrosine; Tyrosinemias | 2006 |
Mice deficient in Cu,Zn-superoxide dismutase are resistant to acetaminophen toxicity.
Topics: Acetaminophen; Alanine Transaminase; Animals; Benzoquinones; Biotransformation; Body Weight; Cytochrome P-450 CYP2E1; Cytochrome P-450 CYP2E1 Inhibitors; Drug Resistance; Enzyme Induction; Glutathione; Glutathione Peroxidase; Glutathione Peroxidase GPX1; Imines; Liver Failure; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Oxidation-Reduction; Oxidative Stress; Peroxynitrous Acid; Superoxide Dismutase; Tyrosine | 2006 |
Non-isotopic tyrosine kinetics using an alanyl-tyrosine dipeptide to assess graft function in liver transplant recipients - a pilot study.
Topics: Adult; Alanine Transaminase; Aspartate Aminotransferases; Dipeptides; Feasibility Studies; Female; Humans; Indocyanine Green; Liver Failure; Liver Function Tests; Liver Transplantation; Male; Metabolic Clearance Rate; Middle Aged; Pilot Projects; Predictive Value of Tests; Tissue Donors; Tyrosine | 2008 |
Liver transplantation in type I tyrosinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Carcinoma, Hepatocellular; Child, Preschool; Follow-Up Studies; Humans; Infant; Liver Cirrhosis; Liver Failure; Liver Neoplasms; Retrospective Studies; Time Factors; Tyrosine | 1995 |
[Surgical and metabolic aspects of liver transplantation for tyrosinemia].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Central Nervous System Diseases; Child; Child, Preschool; Female; Heptanoates; Humans; Infant; Kidney Function Tests; Kidney Transplantation; Liver Failure; Liver Transplantation; Male; Postoperative Care; Preoperative Care; Quebec; Renal Insufficiency; Tyrosine | 1993 |
Pseudotumours of hepatic imaging.
Topics: Adolescent; Adult; Aged; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Gaucher Disease; Humans; Infant; Liver Diseases; Liver Failure; Liver Transplantation; Tomography, X-Ray Computed; Tyrosine | 1996 |
Mutation analysis for prenatal diagnosis of hereditary tyrosinaemia type 1.
Topics: Amino Acid Metabolism, Inborn Errors; Chorionic Villi Sampling; Heterozygote; Humans; Hydrolases; Infant; Liver Failure; Male; Mutation; Tyrosine | 1997 |
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 |
[Favorable outcome of treatment with NTBC of acute liver insufficiency disclosing hereditary tyrosinemia type I].
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Acute Disease; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Cyclohexanones; Enzyme Inhibitors; Female; Follow-Up Studies; Heptanoates; Humans; Infant; Infant, Newborn; Liver Failure; Male; Methionine; Nitrobenzoates; Porphobilinogen Synthase; Treatment Outcome; Tyrosine | 1999 |