s-adenosylmethionine has been researched along with Embryopathies in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (83.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Besley, GT; Fleming, G; Henderson, MJ; Patterson, A; Till, J; Walter, JH | 1 |
| Amoroso, A; Boniotto, M; Braida, L; Casetta, B; Crovella, S; de Vonderweid, U; Luchesi, A | 1 |
| Chisholm, CA; Frerman, FE; Lovell, MA; Roe, CR; Roe, DS; Sweetman, L; Vavelidis, F; Wilson, WG | 1 |
| Burren, KA; Chitty, LS; Copp, AJ; Doudney, K; Dunlevy, LP; Greene, ND; Scott, R; Stanier, P; Stojilkovic-Mikic, T | 1 |
| Ilas, J; Mühl, A; Stöckler-Ipsiroglu, S | 1 |
| Bélanger, L; Bélanger, M; Gourdeau, H; Larochelle, J | 1 |
6 other study(ies) available for s-adenosylmethionine and Embryopathies
| Article | Year |
|---|---|
Bloodspot acylcarnitine and amino acid analysis in cord blood samples: efficacy and reference data from a large cohort study.
Topics: Amino Acids; Blood Chemical Analysis; Blood Specimen Collection; Carnitine; Cohort Studies; Efficiency; False Negative Reactions; Fetal Blood; Fetal Diseases; Humans; Infant, Newborn; Metabolic Diseases; Mothers; Neonatal Screening; Reference Values; Time Factors | 2009 |
A rapid and quantitative mass spectrometry method for determining the concentration of acylcarnitines and aminoacids in amniotic fluid.
Topics: Amino Acids; Amniotic Fluid; Carnitine; Female; Fetal Diseases; Humans; Mass Spectrometry; Metabolic Diseases; Predictive Value of Tests; Pregnancy; Prenatal Diagnosis; Sensitivity and Specificity | 2001 |
Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated alpha-fetoprotein and cystic renal changes.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; alpha-Fetoproteins; Amniocentesis; Amniotic Fluid; Carnitine; Diagnosis, Differential; Fatty Liver; Female; Fetal Diseases; Fetal Growth Retardation; Gestational Age; Humans; Oligohydramnios; Polycystic Kidney Diseases; Pregnancy; Prenatal Diagnosis; Ultrasonography, Prenatal | 2001 |
Abnormal folate metabolism in foetuses affected by neural tube defects.
Topics: Anencephaly; Animals; Antimetabolites; Deoxyuridine; Female; Ferredoxin-NADP Reductase; Fetal Diseases; Fetus; Fibroblasts; Folic Acid; Genotype; Humans; Methylation; Mice; Neural Tube Defects; NIH 3T3 Cells; Polymorphism, Genetic; Pregnancy; S-Adenosylhomocysteine; S-Adenosylmethionine; Spinal Dysraphism | 2007 |
Guanidinoacetate methyltransferase (GAMT) deficiency: non-invasive enzymatic diagnosis of a newly recognized inborn error of metabolism.
Topics: Amniotic Fluid; Cells, Cultured; Chromatography, High Pressure Liquid; Creatine; Female; Fetal Diseases; Fibroblasts; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Lymphocytes; Male; Metabolism, Inborn Errors; Methyltransferases; Pregnancy; Prenatal Diagnosis; S-Adenosylmethionine; Skin | 2000 |
[New observations on fetal liver cirrhosis associated with hereditary tyrosinemia].
Topics: Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Animals; Female; Fetal Diseases; Guinea Pigs; Humans; Liver; Liver Cirrhosis; Pregnancy; Rats; S-Adenosylmethionine; Tyrosine | 1985 |