phenylalanine has been researched along with Disease in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bendlova, B; Bilek, R; Dvorakova, K; Dvorakova, S; Skaba, R; Sykorova, V; Vaclavikova, E; Vlcek, P; Zelinka, T | 1 |
| ANDERSON, JA; ERTEL, R; FISCH, R; GRAVEM, H; McCARTHY, J | 1 |
| Morrow, G | 1 |
3 other study(ies) available for phenylalanine and Disease
| Article | Year |
|---|---|
RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest.
Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Carcinoma, Medullary; Child; Disease; Family; Female; Genetic Association Studies; Germ-Line Mutation; Hirschsprung Disease; Humans; Male; Middle Aged; Multiple Endocrine Neoplasia Type 2a; Neural Crest; Phenylalanine; Polymorphism, Single Nucleotide; Proto-Oncogene Mas; Proto-Oncogene Proteins c-ret; Thyroid Neoplasms; Tyrosine; Young Adult | 2009 |
Two-dose phenylalanine tolerance test for detection of phenylketonuric heterozygotes. Value of tyrosine responses.
Topics: Disease; Diseases in Twins; Drug Tolerance; Heterozygote; Humans; Immune Tolerance; Phenylalanine; Phenylketonurias; Twins; Tyrosine | 1961 |
Latrogenesis imperfecta--a new pediatric problem.
Topics: Amniotic Fluid; Clinical Laboratory Techniques; Cushing Syndrome; Diagnostic Errors; Disease; False Positive Reactions; Female; Health; Humans; Male; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Pregnancy | 1975 |