leucine has been researched along with Congenital Myasthenia 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 | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Govindarajan, R; Singh, S | 1 |
| Colquhoun, D; Shelley, C | 1 |
2 other study(ies) available for leucine and Congenital Myasthenia
| Article | Year |
|---|---|
Presentation and management of congenital myasthenic syndrome with a homozygous Agrin variant (Pro1448Leu).
Topics: Adolescent; Agrin; Cholinesterase Inhibitors; Diagnosis, Differential; Disease Management; Female; Genetic Variation; Homozygote; Humans; Leucine; Myasthenic Syndromes, Congenital; Proline; Pyridostigmine Bromide | 2020 |
A human congenital myasthenia-causing mutation (epsilon L78P) of the muscle nicotinic acetylcholine receptor with unusual single channel properties.
Topics: Acetylcholine; Binding Sites; Cell Line; Dose-Response Relationship, Drug; Humans; Leucine; Likelihood Functions; Mutation; Myasthenic Syndromes, Congenital; Proline; Receptors, Nicotinic | 2005 |