methionine has been researched along with Amyloidosis, Familial in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Atkinson, D; Das, M; Gursky, O; Jayaraman, S; Mei, X | 1 |
| Backman, C; Ihse, E; Lindqvist, P; Suhr, O; Westermark, P; Ybo, A | 1 |
| Baba, HA; Boese, D; Christoph, DC; Erbel, R; Hunold, P; Johnson, KT; Philipp, S; Schlosser, TW | 1 |
3 other study(ies) available for methionine and Amyloidosis, Familial
| Article | Year |
|---|---|
Amyloidogenic mutations in human apolipoprotein A-I are not necessarily destabilizing - a common mechanism of apolipoprotein A-I misfolding in familial amyloidosis and atherosclerosis.
Topics: Amyloidosis, Familial; Apolipoprotein A-I; Atherosclerosis; Humans; Methionine; Mutation; Protein Folding; Structure-Activity Relationship | 2014 |
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 |
Heart failure and cardiac involvement as isolated manifestation of familial form of transthyretin amyloidosis resulting from Val30Met mutation with no clinical signs of polyneuropathy.
Topics: Amyloidosis, Familial; Cardiomyopathies; Echocardiography; Heart Failure; Humans; Immunohistochemistry; Magnetic Resonance Imaging; Male; Methionine; Microscopy, Electron; Middle Aged; Mutation; Prealbumin; Valine | 2009 |