methionine has been researched along with Intraventricular Septal Defects in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Backman, C; Ihse, E; Lindqvist, P; Suhr, O; Westermark, P; Ybo, A | 1 |
| Baumgartner, ER; Bosk, A; Fowler, B; Heinemann, MK; Sieverding, L; Tomaske, M; Trefz, FK | 1 |
2 other study(ies) available for methionine and Intraventricular Septal Defects
| Article | Year |
|---|---|
Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis.
Topics: Abdominal Fat; Adult; Age of Onset; Amino Acid Substitution; Amyloid; Amyloidosis, Familial; Blotting, Western; Cardiomyopathies; Echocardiography; Electrophoresis, Polyacrylamide Gel; Female; Heart Septal Defects, Ventricular; Humans; Male; Methionine; Middle Aged; Prealbumin; Sweden; Valine | 2008 |
CblC/D defect combined with haemodynamically highly relevant VSD.
Topics: Female; Folic Acid; Heart Septal Defects, Ventricular; Homocysteine; Homocystinuria; Humans; Hydroxocobalamin; Infant, Newborn; Lactic Acid; Metabolism, Inborn Errors; Methionine; Methylmalonic Acid | 2001 |