sapropterin has been researched along with Syndrome in 4 studies
| 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 | Studies |
|---|---|
| Blau, N; Demos, M; Khashu, M; Lillquist, Y; Mattman, A; Rupar, A; Scott, P; Senger, C; Setchell, K; Vallance, HD; Waters, PJ | 1 |
| Robertson, D | 1 |
| Matsuo, N | 1 |
| Blair, J; Hagberg, B; Leeming, R; Sahota, A | 1 |
2 review(s) available for sapropterin and Syndrome
| Article | Year |
|---|---|
Genetics and molecular biology of hypotension.
Topics: Animals; Aromatic-L-Amino-Acid Decarboxylases; Autonomic Nervous System; Biopterins; Blood Pressure; Dopamine beta-Hydroxylase; Humans; Hypotension; Mitral Valve Prolapse; Monoamine Oxidase; Phenotype; Syndrome | 1994 |
Hyperphenylalaninemia syndromes: current status of diagnosis and management.
Topics: Amino Acid Metabolism, Inborn Errors; Biopterins; Female; Humans; Hydroxylation; Infant, Newborn; Phenylalanine; Phenylketonurias; Pregnancy; Prenatal Diagnosis; Syndrome | 1988 |
2 other study(ies) available for sapropterin and Syndrome
| Article | Year |
|---|---|
Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: a unique patient or a novel metabolic disorder?
Topics: Amino Acids; Biopterins; Fatal Outcome; Gene Deletion; Hemochromatosis; Humans; Infant, Newborn; Kidney Tubules; Liver Failure; Male; Phenylketonurias; Syndrome | 2005 |
Tetrahydrobiopterin metabolism in the Rett disease.
Topics: Biopterins; Child; Dihydropteridine Reductase; Female; Humans; Intellectual Disability; NADH, NADPH Oxidoreductases; Neurocognitive Disorders; Pteridines; Stereotyped Behavior; Syndrome | 1985 |