tyrosine has been researched along with Porphyrias in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 12 (92.31) | 18.7374 |
| 1990's | 1 (7.69) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| DRUYAN, R; HAEGER-ARONSEN, B; WALDENSTROEM, J | 1 |
| Cole, DE; Crocker, JF; Moss, MA; Tithecott, GA | 1 |
| Mowat, AP | 2 |
| Hosszú, E; Kálmánchey, R; Klujber, V; Sallai, A; Szönyi, L | 1 |
| Frykholm, BC; Lamon, JM; Tschudy, DP | 1 |
| Berry, HK; Emmett, EA; Finelli, VN; Petering, HG; Strife, CF; Zuroweste, EL | 1 |
| Sassa, S | 1 |
| Irons, M; Levy, HL | 1 |
| Balda, BR; Lukacs, I | 1 |
| Gerald, PS; Kang, ES | 1 |
| Keterlers, JY; Warembourg, H | 1 |
3 review(s) available for tyrosine and Porphyrias
| Article | Year |
|---|---|
Hepatic Disorders.
Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Cystic Fibrosis; Female; Fructose Intolerance; Fructose-1,6-Diphosphatase Deficiency; Galactosemias; Glycogen Storage Disease; Humans; Infant; Infant, Newborn; Liver Diseases; Male; Polycystic Kidney Diseases; Porphyrias; Tyrosine; Urea | 1982 |
Metabolic syndromes with dermatologic manifestations.
Topics: Albinism; Alkaptonuria; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Amino Acids; Biotinidase; Carbohydrate Metabolism; Eczema; Hartnup Disease; Homocystinuria; Humans; Keratosis; Menkes Kinky Hair Syndrome; Metabolic Diseases; Phenylketonurias; Porphyrias; Skin Diseases; Steryl-Sulfatase; Sulfatases; Tyrosine; Urea | 1986 |
[Molecular biologic aspects in dermatology demonstrated by some hereditary enzyme defects].
Topics: Albinism; Alkaptonuria; Anemia, Sickle Cell; Chromosomes; Hartnup Disease; Humans; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Models, Chemical; Molecular Biology; Phenylalanine; Phenylketonurias; Porphyrias; Skin Diseases; Tyrosine | 1968 |
10 other study(ies) available for tyrosine and Porphyrias
| Article | Year |
|---|---|
RENAL MECHANISM FOR EXCRETION OF PORPHYRIN PRECURSORS IN PATIENTS WITH ACUTE INTERMITTENT PORPHYRIA AND CHRONIC LEAD POISONING.
Topics: Amino Acids; Biomedical Research; Blood; Creatine; Creatinine; Fluids and Secretions; Humans; Kidney; Lead Poisoning; Levulinic Acids; Porphyria, Acute Intermittent; Porphyrias; Porphyrins; Pyrroles; Tryptophan; Tyrosine; Urine | 1965 |
Alphaxalone/alphadolone and porphyria.
Topics: Alfaxalone Alfadolone Mixture; Chemical and Drug Induced Liver Injury; Child; Humans; Male; Medication Errors; Porphyrias; Tyrosine | 1984 |
[Late onset type I tyrosinemia].
Topics: alpha-Fetoproteins; Amino Acid Metabolism, Inborn Errors; Biopsy; Child, Preschool; Cyclohexanones; Enzyme Inhibitors; Female; Humans; Liver Cirrhosis; Nitrobenzoates; Palliative Care; Porphyrias; Tyrosine | 1997 |
Tyrosinemia with aminolevulinic dehydratase deficiency.
Topics: Humans; Porphobilinogen Synthase; Porphyrias; Tyrosine | 1978 |
Tyrosinemia with acute intermittent porphyria: aminolevulinic acid dehydratase deficiency related to elevated urinary aminolevulinic acid levels.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Catecholamines; Female; Humans; Hydro-Lyases; Levulinic Acids; Porphobilinogen Synthase; Porphyrias; Renin; Tyrosine | 1977 |
[Significance of delta-aminolevulinic acid analysis in clinical tests].
Topics: Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Chromatography, Gas; Chromatography, High Pressure Liquid; Colorimetry; Humans; Lead Poisoning; Levulinic Acids; Liver Diseases; Porphyrias; Reference Values; Tyrosine | 1989 |
Liver disorders in children: the indications for liver replacement in parenchymal and metabolic diseases.
Topics: Amino Acid Metabolism, Inborn Errors; Budd-Chiari Syndrome; Child; Cholangitis; Crigler-Najjar Syndrome; Hepatitis, Chronic; Hepatolenticular Degeneration; Humans; Infant; Liver Cirrhosis; Liver Diseases; Liver Transplantation; Porphyrias; Tyrosine | 1987 |
Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Metabolism, Inborn Errors; Carrier State; Ceruloplasmin; Cholinesterases; Cystic Fibrosis; Diagnostic Services; Female; Galactosemias; Genetic Diseases, Inborn; Hepatolenticular Degeneration; Humans; Infant; Infant, Newborn; Male; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Phenylketonurias; Porphyrias; Tyrosine; World Health Organization | 1968 |
Hereditary tyrosinemia and abnormal pyrrole metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Female; Fructose; Humans; Infant; Levulinic Acids; Liver Cirrhosis; Methionine; Oxidoreductases; Porphyrias; Porphyrins; Pyrroles; Renal Tubular Transport, Inborn Errors; Tyrosine | 1970 |
[Clinical study on the cardiac tolerance and biological action of a lyophilized thyroid extract administered orally. Apropos of 30 cases].
Topics: Administration, Oral; Adolescent; Adult; Aged; Female; Heart; Humans; Hypercholesterolemia; Hypertension; Kidney Diseases; Liver Cirrhosis; Male; Middle Aged; Monoiodotyrosine; Obesity Hypoventilation Syndrome; Porphyrias; Thyroid Hormones; Tyrosine | 1968 |