phenylalanine has been researched along with Carbohydrate Metabolism, Inborn Error in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (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 |
|---|---|
| Brady, RO | 2 |
| Royer, P | 1 |
| Bakker, HD; de Bree, PK; van Sprang, FJ; Wadman, SK | 1 |
| Levy, HL | 1 |
| Gjessing, LR; Halvorsen, S; Lindemann, R; Löken, AC; Merton, B | 1 |
2 review(s) available for phenylalanine and Carbohydrate Metabolism, Inborn Error
| Article | Year |
|---|---|
Inherited metabolic diseases and pathogenesis of mental retardation.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain; Carbohydrate Metabolism, Inborn Errors; Cytochrome Reductases; Deoxyglucose; Dihydrolipoamide Dehydrogenase; Energy Metabolism; Gangliosides; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Phenylalanine; Pyruvate Dehydrogenase Complex Deficiency Disease | 1978 |
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 |
4 other study(ies) available for phenylalanine and Carbohydrate Metabolism, Inborn Error
| Article | Year |
|---|---|
Inherited metabolic diseases of the nervous system.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Gangliosidoses; Glutathione; Glycine; Glycogen Storage Disease Type II; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Mucopolysaccharidoses; Nerve Tissue Proteins; Nervous System Diseases; Phenylalanine; Phenylketonurias | 1976 |
[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 |
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 |
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 |