leucine has been researched along with Alexander Disease 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 | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ichihashi, J; Kitada, M; Kusunoki, S; Mistui, Y; Nakagawa, M; Nishikawa, Y; Sasayama, H; Suzuki, H; Yoshida, T | 1 |
| Adachi, M; Hayasaka, K; Kato, M; Sawaishi, Y; Shiihara, T | 1 |
2 other study(ies) available for leucine and Alexander Disease
| Article | Year |
|---|---|
Late-onset Alexander disease with a V87L mutation in glial fibrillary acidic protein (GFAP) and calcifying lesions in the sub-cortex and cortex.
Topics: Adult; Alexander Disease; Brain; Calcinosis; DNA Mutational Analysis; Female; Glial Fibrillary Acidic Protein; Humans; Leucine; Magnetic Resonance Imaging; Mutation; Valine | 2012 |
Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP.
Topics: Alexander Disease; Brain; Child; DNA Mutational Analysis; Exons; Female; Glial Fibrillary Acidic Protein; Humans; Infant; Leucine; Magnetic Resonance Imaging; Male; Mutation; Proline; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger | 2004 |