valine has been researched along with Alexander Disease 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 |
|---|---|
| Ichihashi, J; Kitada, M; Kusunoki, S; Mistui, Y; Nakagawa, M; Nishikawa, Y; Sasayama, H; Suzuki, H; Yoshida, T | 1 |
| Funatsuka, M; Hattori, N; Ishigaki, K; Ito, Y; Kodaira, K; Nakano, K; Osawa, M; Saito, K; Sawaishi, Y | 1 |
| Christen, HJ; Das, AM; Donnerstag, F; Hagedorn, M; Hartmann, H; Herchenbach, J; Ledaal, P; Lücke, T; Meins, M; Stephani, U | 1 |
3 other study(ies) available for valine 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 |
TRH therapy in a patient with juvenile Alexander disease.
Topics: Alexander Disease; Aspartic Acid; Child; DNA Mutational Analysis; Female; Glial Fibrillary Acidic Protein; Humans; Magnetic Resonance Imaging; Mutation; Thyrotropin-Releasing Hormone; Valine | 2006 |
Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease.
Topics: Age of Onset; Alanine; Alexander Disease; Cysteine; DNA Mutational Analysis; Exons; Female; Frontal Lobe; Glial Fibrillary Acidic Protein; Humans; Infant; Magnetic Resonance Imaging; Male; Mutation; Protein Structure, Tertiary; Tyrosine; Valine | 2007 |