s-adenosylmethionine has been researched along with BH4 Deficiency in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 4 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baud, O; Benoist, JF; Bower, A; Imbard, A; Pichard, S; Rigal, O; Schiff, M | 1 |
| Gao, X; Gu, X; Han, F; Han, L; Ji, W; Qiu, W; Wang, Y; Ye, J; Zhang, H | 1 |
| Arias, A; Artuch, R; Campistol, J; Desviat, LR; Farré, G; García-Cazorla, A; García-Villoria, J; Merinero, B; Ribes, A; Rodríguez-Pombo, P; Sempere, A; Vilaseca, MA | 1 |
| Andria, G; Parenti, G; Scala, I | 1 |
| Debreceni, B; Farkas, V; Fischer, GM; Laszlo, A; Nemeti, B; Sandor, A; Schaffer, Z; Somogyi, C | 1 |
| Hyland, K; Surtees, R | 1 |
1 review(s) available for s-adenosylmethionine and BH4 Deficiency
| Article | Year |
|---|---|
Universal screening for inherited metabolic diseases in the neonate (and the fetus).
Topics: Acyl-CoA Dehydrogenase; Amino Acids; Carnitine; DNA; DNA Mutational Analysis; Female; Gestational Age; Humans; Infant, Newborn; Metabolism, Inborn Errors; Neonatal Screening; Paper; Phenylketonurias; Pregnancy; Prenatal Diagnosis; Tandem Mass Spectrometry | 2012 |
5 other study(ies) available for s-adenosylmethionine and BH4 Deficiency
| Article | Year |
|---|---|
Diagnostic contribution of metabolic workup for neonatal inherited metabolic disorders in the absence of expanded newborn screening.
Topics: Amino Acids; Carnitine; Female; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intensive Care Units, Neonatal; Male; Maple Syrup Urine Disease; Metabolic Diseases; Neonatal Screening; Paris; Phenylketonurias; Propionic Acidemia | 2019 |
Spectrum analysis of common inherited metabolic diseases in Chinese patients screened and diagnosed by tandem mass spectrometry.
Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carboxylic Acids; Carnitine; Child; Child, Preschool; China; Fatty Acids; Female; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Metabolic Diseases; Middle Aged; Oxidation-Reduction; Phenylketonurias; Tandem Mass Spectrometry | 2015 |
Study of inborn errors of metabolism in urine from patients with unexplained mental retardation.
Topics: Adenylosuccinate Lyase; Adolescent; Adult; Aged; Carnitine; Child; Child, Preschool; Chromium; Cohort Studies; Creatine; Female; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Middle Aged; Phenylketonurias; Purines; Pyrimidines | 2010 |
Metabolism of carnitine in phenylacetic acid-treated rats and in patients with phenylketonuria.
Topics: Adult; Animals; Betaine; Carnitine; Female; Glutamic Acid; Homogentisic Acid; Humans; Ketoglutaric Acids; Liver; Male; Mass Spectrometry; Phenylacetates; Phenylketonurias; Phenylpyruvic Acids; Rats; Rats, Wistar | 2000 |
L-3,4-dihydroxyphenylalanine (levodopa) lowers central nervous system S-adenosylmethionine concentrations in humans.
Topics: Adolescent; Akinetic Mutism; Biopterins; Child, Preschool; Humans; Infant; Levodopa; Methionine; NADH, NADPH Oxidoreductases; Phenylketonurias; Pyridoxine; S-Adenosylmethionine; Tetrahydrofolates; Tyrosine | 1990 |