phenylalanine and Lesch-Nyhan Syndrome

phenylalanine has been researched along with Lesch-Nyhan Syndrome in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (50.00)	18.7374
1990's	1 (25.00)	18.2507
2000's	1 (25.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Arnold, LA; Egami, K; Hyland, K; Jinnah, HA; Kasim, S	1
Omenn, GS	1
Halliday, D; Pacy, PJ; Thompson, GN; Watts, RW	1
Harper, PS	1

Reviews

1 review(s) available for phenylalanine and Lesch-Nyhan Syndrome

Article	Year
Inborn errors of metabolism: clues to understanding human behavioral disorders. Behavior genetics, 1976, Volume: 6, Issue:3 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

Article

Year

Inborn errors of metabolism: clues to understanding human behavioral disorders.

Behavior genetics, 1976, Volume: 6, Issue:3

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

Other Studies

3 other study(ies) available for phenylalanine and Lesch-Nyhan Syndrome

Article	Year
Tetrahydrobiopterin deficiency and dopamine loss in a genetic mouse model of Lesch-Nyhan disease. Journal of inherited metabolic disease, 2004, Volume: 27, Issue:2 Topics: Animals; Biopterins; Corpus Striatum; Disease Models, Animal; Dopamine; Dopamine Agents; Hypoxanthine Phosphoribosyltransferase; Lesch-Nyhan Syndrome; Levodopa; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Phenylalanine; Tyrosine	2004
Protein metabolism in phenylketonuria and Lesch-Nyhan syndrome. Pediatric research, 1990, Volume: 28, Issue:3 Topics: Adolescent; Adult; Amino Acids; Female; Growth Disorders; Humans; Lesch-Nyhan Syndrome; Leucine; Male; Middle Aged; Phenylalanine; Phenylketonurias; Proteins	1990
Inborn errors of metabolism-the relationship of clinical and biochemical abnormalities. Acta Universitatis Carolinae. Medica. Monographia, 1973, Volume: 56 Topics: Cystathionine; Diseases in Twins; Glutamine; Homocystinuria; Humans; Infant, Newborn; Intellectual Disability; Lesch-Nyhan Syndrome; Metabolism, Inborn Errors; NADH, NADPH Oxidoreductases; Phenotype; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias	1973