tyrosine has been researched along with Carbohydrate Metabolism, Inborn Error in 15 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 15 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| FINCKE, ML | 1 |
| Beaufils, F; Bourrillon, A; Mercier, JC; Odievre, M | 1 |
| Benjafield, JG; Rutter, LF | 1 |
| Gjessing, LR; Halvorsen, S; Lindemann, R; Merton, B | 1 |
| Royer, P | 1 |
| Dozić, S; Hajduković, R; Sindjić, M; Vulović, D | 1 |
| Bakker, HD; de Bree, PK; van Sprang, FJ; Wadman, SK | 1 |
| Bickel, H; Schmidt, H; Schürrle, L | 1 |
| Levy, HL | 1 |
| Odievre, M | 1 |
| Horecker, BL; Morse, DE | 1 |
| Davidson, M; Silverberg, M | 1 |
| Heusden, A; Legat, C; Monard, Y; Renson, P; Stainier, L; Willems, C | 1 |
| Gjessing, LR; Halvorsen, S; Lindemann, R; Löken, AC; Merton, B | 1 |
| Alexander, FW; Grant, DB; Seakins, JW | 1 |
3 review(s) available for tyrosine and Carbohydrate Metabolism, Inborn Error
| Article | Year |
|---|---|
Dietary treatment of inborn errors of amino acid and carbohydrate metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Child; Child Development; Child Nutritional Physiological Phenomena; Child, Preschool; Cystinosis; Diet Therapy; Galactose; Glucose; Histidine; Homocystinuria; Humans; Infant; Infant Nutrition Disorders; Infant, Newborn; Lactose Intolerance; Malabsorption Syndromes; Maple Syrup Urine Disease; Phenylketonurias; Sucrose; Tyrosine | 1973 |
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 |
The mechanism of action of aldolases.
Topics: Amino Acid Sequence; Animals; Bacteria; Binding Sites; Biological Evolution; Carbohydrate Metabolism, Inborn Errors; Cattle; Chelating Agents; Chemistry, Organic; Cysteine; Fructose; Fructose-Bisphosphate Aldolase; Genetics; Histidine; Liver; Lysine; Metals; Models, Chemical; Molecular Weight; Muscles; Organ Specificity; Organic Chemistry Phenomena; Phosphates; Rabbits; Rats; Saccharomyces; Tyrosine | 1968 |
12 other study(ies) available for tyrosine and Carbohydrate Metabolism, Inborn Error
| Article | Year |
|---|---|
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 |
[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 |
Significance of metabolic disorders in schizophrenia.
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Dopamine; Female; Humans; Male; Methylation; Schizophrenia; Tyrosine | 1973 |
Fructosaemia-"acute-tyrosinosis".
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Diagnosis, Differential; Fructose; Humans; Infant; Male; Methionine; Tyrosine | 1969 |
[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 |
[Disorders in the tyrosine metabolism. II. Tyrosinemia - a congenital metabolic disorder].
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Diagnosis, Differential; Female; Humans; Hypophosphatemia, Familial; Infant; Tyrosine | 1974 |
Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis".
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carbohydrate Metabolism, Inborn Errors; Chromatography, Gas; Cystathionine; Dietary Carbohydrates; Female; Fructose-1,6-Diphosphatase Deficiency; Fructose-Bisphosphatase; Humans; Infant; Lactates; Methionine; Phenylalanine; Sucrose; Tyrosine | 1974 |
[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 |
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 |
[Hypertyrosinemia with hypermethioninemia in the newborn in a case of fructose intolerance].
Topics: Amino Acids; Carbohydrate Metabolism, Inborn Errors; Female; Fructose; Humans; Infant; Infant, Newborn; Methionine; Tyrosine | 1971 |
Amino acid metabolism in hereditary fructosemia.
Topics: Amino Acids; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Chromatography, Paper; Female; Fructose; Fructose-Bisphosphate Aldolase; Humans; Infant; Infant, Newborn; Liver; Male; Phenylalanine; Tyrosine | 1970 |
Abnormal tyrosine metabolism in hereditary fructose intolerance.
Topics: Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Fructose; Humans; Infant; Lactates; Liver Function Tests; Methionine; Phenylacetates; Tyrosine | 1970 |