lysine has been researched along with Adult Onset Nemaline Myopathy 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 |
|---|---|
| Kim, DS; Kim, HS; Kim, SY; Lee, CH; Park, YE; Yang, DH | 1 |
| Darin, N; Kyllerman, M; Ohlsson, M; Oldfors, A; Tajsharghi, H | 1 |
| Bertini, E; Boldrini, R; D'Amico, A; Feng, JJ; Graziano, C; Jacques, A; Laing, N; Limongelli, G; Marston, SB; Nowak, KJ; Pacileo, G; Petrini, S; Porfirio, B; Santorelli, FM; Sewry, CA | 1 |
3 other study(ies) available for lysine and Adult Onset Nemaline Myopathy
| Article | Year |
|---|---|
Nemaline myopathy and non-fatal hypertrophic cardiomyopathy caused by a novel ACTA1 E239K mutation.
Topics: Actins; Amino Acid Sequence; Cardiomyopathy, Hypertrophic; Glutamic Acid; Humans; Lysine; Male; Molecular Sequence Data; Muscle, Skeletal; Myopathies, Nemaline; Point Mutation; Young Adult | 2011 |
Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1).
Topics: Actins; Aspartic Acid; DNA Mutational Analysis; Exons; Female; Follow-Up Studies; Genetic Carrier Screening; Glutamic Acid; Glycine; Heterozygote; Humans; Lysine; Male; Microscopy, Electron; Muscle, Skeletal; Mutation; Myopathies, Nemaline | 2004 |
Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation.
Topics: Actinin; Actins; Amino Acid Substitution; Cardiomyopathy, Hypertrophic, Familial; Child, Preschool; DNA Mutational Analysis; Fatal Outcome; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Humans; Lysine; Male; Muscle Contraction; Muscle Fibers, Skeletal; Muscle, Skeletal; Mutation, Missense; Myocardium; Myopathies, Nemaline | 2006 |