phenylalanine has been researched along with Mucopolysaccharidoses in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (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 | 1 |
| Omenn, GS | 1 |
| Hsia, DY | 1 |
| Narayanan, HS; Rao, BS; Reddy, GN | 1 |
1 review(s) available for phenylalanine and Mucopolysaccharidoses
| Article | Year |
|---|---|
Inborn errors of metabolism: clues to understanding human behavioral disorders.
Topics: Adrenal Hyperplasia, Congenital; Brain; Galactosemias; Glycine; Hepatolenticular Degeneration; Heterozygote; Homocystinuria; Humans; Lesch-Nyhan Syndrome; Maple Syrup Urine Disease; Mental Disorders; Metabolism, Inborn Errors; Mucopolysaccharidoses; Phenylalanine; Phenylketonurias; Porphyrias; Sphingolipidoses; Turner Syndrome; Urea | 1976 |
3 other study(ies) available for phenylalanine and Mucopolysaccharidoses
| 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 |
The aminoacidopathies.
Topics: Amino Acid Metabolism, Inborn Errors; Cells, Cultured; Clone Cells; Culture Techniques; Female; Fibroblasts; Galactosemias; Genes, Recessive; Heterozygote; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Mucopolysaccharidoses; Phenylalanine; Phenylketonurias; Sex Factors | 1972 |
A clinical and biochemical survey of 729 cases of mental subnormality.
Topics: Angiomatosis; Child; Child, Preschool; Congenital Hypothyroidism; Down Syndrome; Female; Hartnup Disease; Humans; India; Infant; Intellectual Disability; Laurence-Moon Syndrome; Lipidoses; Male; Marfan Syndrome; Microcephaly; Mucopolysaccharidoses; Phenylalanine; Phenylketonurias; Sex Factors; Syphilis, Congenital | 1971 |