tyrosine has been researched along with Classic Galactosemia in 37 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 31 (83.78) | 18.7374 |
| 1990's | 3 (8.11) | 18.2507 |
| 2000's | 1 (2.70) | 29.6817 |
| 2010's | 2 (5.41) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abdul Nasir, NA; Agarwal, R; Alyautdin, R; Ismail, NM; Tripathy, M; Vasudevan, S | 1 |
| Bhatia, KP; Burke, D; Carecchio, M; Chandrashekar, HS; Edwards, MJ; Footitt, EJ; Kojovic, M; Lachmann, RH; Murphy, E; Parees, I; Rubio-Agusti, I | 1 |
| Koppolu, P; Kowluru, RA | 1 |
| ROBINSON, A | 1 |
| FINCKE, ML | 1 |
| Scriver, CR | 1 |
| Mowat, AP | 1 |
| Katz, AJ | 1 |
| Alm, J; Larsson, A; Rosenqvist, U | 1 |
| Mamunes, P | 1 |
| Alm, J; Larsson, A | 1 |
| Kumada, S; Okaniwa, M | 1 |
| Kohgo, Y; Ono, M | 1 |
| Igarashi, T | 1 |
| Hill, GN; Pollard, AC; Robertson, EF | 1 |
| Grand, RJ; Katz, AJ; Watkins, JB | 1 |
| Finegold, MJ | 1 |
| Dimmick, JE; Hardwick, DF | 1 |
| Beaufils, F; Bourrillon, A; Mercier, JC; Odievre, M | 1 |
| Rigilano, JC; Stevens, MB; Wilson, CC | 1 |
| Kawamura, M | 1 |
| Mowat, A | 1 |
| Donnell, GN; Koch, R; Lieberman, E; Shaw, KN | 1 |
| Royer, P | 1 |
| Levy, HL | 1 |
| Schmid-Rüter, E | 1 |
| Odievre, M | 1 |
| Hruban, Z; Jevtic, MM; Thorp, FK | 1 |
| Grenier, A; Laberge, C | 1 |
| Bozkowa, K; Cabalska, MB | 1 |
| Davidson, M; Silverberg, M | 1 |
| Knoll, E; Scheibenreiter, S; Schmierer, G; Schön, R; Thalhammer, O | 1 |
| Collombel, C; Cotte, J; David, M; Dutruge, J; Jeune, M; Michel, M | 1 |
| Giovannini, M | 1 |
9 review(s) available for tyrosine and Classic Galactosemia
| 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 |
Neonatal screening tests.
Topics: Adenosine Deaminase; Anemia, Sickle Cell; Biological Assay; Costs and Cost Analysis; Galactosemias; Histidine; Homocystinuria; Humans; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Tyrosine; United States | 1980 |
[Progressive neuronal degeneration and childhood cirrhosis].
Topics: Galactosemias; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Infant; Liver Cirrhosis; Metabolism, Inborn Errors; Peripheral Nervous System Diseases; Tyrosine | 1995 |
[Liver cirrhosis associated with metabolic disorders].
Topics: alpha 1-Antitrypsin; alpha 1-Antitrypsin Deficiency; Galactosemias; Glycogen Storage Disease; Hemochromatosis; Hepatolenticular Degeneration; Humans; Liver Cirrhosis; Metabolism, Inborn Errors; Tyrosine | 1995 |
[Fanconi syndrome].
Topics: Acidosis; Amino Acids; Cystine; Cytochrome-c Oxidase Deficiency; Fanconi Syndrome; Fructose Intolerance; Galactosemias; Glycogen Storage Disease; Humans; Kidney Tubules, Proximal; Oculocerebrorenal Syndrome; Tyrosine | 1998 |
Neonatal hepatitis: a diagnostic approach.
Topics: alpha 1-Antitrypsin Deficiency; Biliary Tract; Cholestasis; Fructose Intolerance; Galactosemias; Hepatitis; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infections; Jaundice, Neonatal; Parenteral Nutrition; Tyrosine | 1977 |
Cholestatic syndromes in infancy.
Topics: Anemia, Hemolytic; Bile; Bile Ducts; Cholestasis; Chromosome Aberrations; Chromosome Disorders; Fasting; Fructose Intolerance; Galactosemias; Histiocytosis, Langerhans-Cell; Humans; Infant; Infant, Newborn; Infections; Jaundice, Neonatal; Liver; Liver Cirrhosis; Niemann-Pick Diseases; Nutritional Physiological Phenomena; Syndrome; Tyrosine | 1976 |
Metabolic cirrhoses of infancy and early childhood.
Topics: Amino Acid Metabolism, Inborn Errors; Cystic Fibrosis; Cystinosis; Fructose Intolerance; Galactosemias; Genetics, Medical; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Iatrogenic Disease; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Liver; Liver Cirrhosis; Metabolism, Inborn Errors; Mucopolysaccharidoses; Niemann-Pick Diseases; Polycystic Kidney Diseases; Tyrosine | 1976 |
Genetic screening.
Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine | 1973 |
28 other study(ies) available for tyrosine and Classic Galactosemia
| Article | Year |
|---|---|
Effects of topically applied tocotrienol on cataractogenesis and lens redox status in galactosemic rats.
Topics: Administration, Topical; Animals; Anterior Eye Segment; Catalase; Cataract; Disease Progression; Emulsions; Eye Proteins; Galactosemias; Glutathione; Lens, Crystalline; Liposomes; Malondialdehyde; Nitric Oxide Synthase Type II; Oxidation-Reduction; Particle Size; Rats; Rats, Sprague-Dawley; Static Electricity; Stress, Physiological; Superoxide Dismutase; Tocotrienols; Tyrosine; Viscosity | 2014 |
Movement disorders in adult patients with classical galactosemia.
Topics: Adult; Anti-Dyskinesia Agents; Benzamides; Botulinum Toxins; Brain; Cross-Sectional Studies; Databases, Factual; Female; Galactosemias; Humans; Magnetic Resonance Imaging; Male; Movement Disorders; Muscarinic Antagonists; Retrospective Studies; Severity of Illness Index; Trihexyphenidyl; Tyrosine; Young Adult | 2013 |
Termination of experimental galactosemia in rats, and progression of retinal metabolic abnormalities.
Topics: Animals; Disease Progression; Drug Administration Schedule; Galactose; Galactosemias; Glutathione; Hexoses; Lipid Peroxides; Male; Metabolic Diseases; Nitric Oxide Synthase; Nitric Oxide Synthase Type II; Oxidative Stress; Protein Kinase C; Rats; Rats, Sprague-Dawley; Retina; Retinal Diseases; Tyrosine | 2002 |
THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES. A PRESUMED TEST FOR HETEROZYGOUS CARRIERS OF THE GALACTOSEMIC DEFECT.
Topics: Benzamides; Carrier State; Clinical Enzyme Tests; Erythrocytes; Galactokinase; Galactosemias; Galactosephosphates; Heterozygote; Humans; Phosphotransferases; Tyrosine; UDPglucose-Hexose-1-Phosphate Uridylyltransferase; UTP-Hexose-1-Phosphate Uridylyltransferase | 1963 |
INBORN ERRORS OF METABOLISM.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Classification; Clinical Laboratory Techniques; Galactosemias; Genetics, Medical; Humans; Intellectual Disability; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Maple Syrup Urine Disease; Mass Screening; Phenylketonurias; Tyrosine | 1965 |
Diagnosis and treatment: interpreting the positive screening test in the newborn infant.
Topics: Amino Acid Metabolism, Inborn Errors; Clinical Laboratory Techniques; Diagnosis, Differential; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylketonurias; Tyrosine | 1967 |
Diagnostic procedures in the evaluation of hepatic diseases. Metabolic errors.
Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Child; Fructose Intolerance; Galactosemias; Hepatolenticular Degeneration; Humans; Infant, Newborn; Liver Diseases; Metabolism, Inborn Errors; Phenotype; Tyrosine | 1983 |
Health economic analysis of the Swedish neonatal metabolic screening programme. A method of optimizing routines.
Topics: Amino Acid Metabolism, Inborn Errors; Cost-Benefit Analysis; Galactosemias; Histidine; Homocystinuria; Humans; Infant, Newborn; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Sweden; Tyrosine | 1982 |
Evaluation of a nation-wide neonatal metabolic screening programme in Sweden 1965-1979.
Topics: Evaluation Studies as Topic; Galactosemias; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Sweden; Tyrosine | 1981 |
Evaluation of a state-wide neonatal screening programme.
Topics: alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Australia; Evaluation Studies as Topic; Follow-Up Studies; Galactosemias; Histidine; Humans; Hypothyroidism; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine | 1979 |
[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 |
Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.
Topics: Amino Acid Metabolism, Inborn Errors; Argininosuccinic Acid; Australia; Cystinuria; Ethnicity; Europe; Galactosemias; Genetics, Population; Hartnup Disease; Histidine; Homocystinuria; Humans; Inbreeding; Infant, Newborn; Israel; Japan; Maple Syrup Urine Disease; Mass Screening; New Zealand; North America; Phenylketonurias; Tyrosine | 1975 |
State screening for metabolic disorders in newborns.
Topics: Adrenal Hyperplasia, Congenital; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Biotinidase; Congenital Hypothyroidism; Cystic Fibrosis; Galactosemias; Homocystinuria; Humans; Hypothyroidism; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine; United States | 1988 |
[Laboratory examinations for inborn errors of metabolism].
Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Gas; Computers; Congenital Hypothyroidism; Galactosemias; Gas Chromatography-Mass Spectrometry; Homocystinuria; Humans; Japan; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine | 1986 |
The management of metabolic disorders of the liver.
Topics: alpha 1-Antitrypsin Deficiency; Child, Preschool; Fructose Intolerance; Galactosemias; Genetic Counseling; Glycogen Storage Disease; Hepatolenticular Degeneration; Humans; Hydrolases; Infant; Infant, Newborn; Liver Diseases; Metabolic Diseases; Phenotype; Prognosis; Tyrosine | 1985 |
Cystathioninuria.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carcinoma, Hepatocellular; Child, Preschool; Cysteine; Diet Therapy; Female; Galactosemias; Glycogen; Humans; Infant; Intellectual Disability; Liver Neoplasms; Male; Maple Syrup Urine Disease; Methionine; Middle Aged; Neuroblastoma; Phenylketonurias; Portal Vein; Pyridoxine; Serine; Sulfisoxazole; Tyrosine | 1967 |
[Dietetics in hereditary enzyme deficiencies].
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Diarrhea, Infantile; Diet Therapy; Galactosemias; Homocystinuria; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Phenylalanine; Phenylketonurias; Tyrosine; Valine | 1970 |
[Screening results for inborn errors of metabolism in Western Europe].
Topics: Denmark; Europe; Evaluation Studies as Topic; France; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; International Cooperation; Ireland; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Netherlands; Phenylketonurias; Preventive Medicine; Switzerland; Tyrosine; United Kingdom | 1973 |
Collective results of mass screening for inborn metabolic errors in eight European countries.
Topics: Belgium; Denmark; France; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; Ireland; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Netherlands; Phenylketonurias; Switzerland; Tyrosine; United Kingdom | 1973 |
[Acute metabolic liver in infants. Remarks on a practical approach].
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Fructose; Galactosemias; Humans; Infant; Infant, Newborn; Liver; Liver Diseases; Tyrosine | 1973 |
Hereditary tyrosinemia with hyperplasia and hypertrophy of juxtaglomerular apparatus.
Topics: Autopsy; Female; Galactosemias; Humans; Hyperplasia; Hypertrophy; Infant; Juxtaglomerular Apparatus; Kidney; Kidney Diseases; Liver; Metabolism, Inborn Errors; Pancreas; Phenylpyruvic Acids; Tyrosine | 1974 |
[Detection of hereditary metabolic diseases in Quebec].
Topics: Amino Acid Metabolism, Inborn Errors; Fluorometry; Galactosemias; Government Agencies; Humans; Hypothyroidism; Infant, Newborn; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Quebec; Radioimmunoassay; Tyrosine | 1974 |
Letter: Frequency of some metabolic disorders in Poland.
Topics: Biological Assay; Galactosemias; Histidine; Humans; Infant, Newborn; Mass Screening; Phenylalanine; Phenylketonurias; Poland; Tyrosine | 1974 |
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 |
Nutritional requirements of infants and children with liver disease.
Topics: Adolescent; Bile; Body Weight; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Cystic Fibrosis; Female; Galactosemias; Glycogen; Hepatitis A; Hepatolenticular Degeneration; Humans; India; Infant; Infant Nutritional Physiological Phenomena; Liver Diseases; Male; Tyrosine | 1970 |
[5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report].
Topics: Amino Acid Metabolism, Inborn Errors; Austria; Child, Preschool; Chromatography, Thin Layer; Diet Therapy; Economics, Medical; Follow-Up Studies; Galactosemias; Glycine; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Metal Metabolism, Inborn Errors; Multiphasic Screening; Phenylketonurias; Proline; Time Factors; Tyrosine | 1972 |
[Transient hypertyrosinemia secondary to hepatic involvement. 2 cases of different etiologies (galactosemia, hepatitis)].
Topics: Female; Galactosemias; Hepatitis; Humans; Infant; Infant, Newborn; Liver Diseases; Male; Methionine; Tyrosine | 1970 |
[Current views on therapy of some dysmetabolic oligophrenias].
Topics: Child, Preschool; Diet Therapy; Galactosemias; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Intellectual Disability; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine | 1967 |