valine has been researched along with Frontotemporal Lobar Degeneration 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 | 0 (0.00) | 29.6817 |
| 2010's | 3 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cruts, M; De Deyn, PP; Engelborghs, S; Gijselinck, I; Mattheijssens, M; Peeters, K; Sleegers, K; Van Broeckhoven, C; Van den Broeck, M; van der Zee, J; Van Langenhove, T; Vandenberghe, R | 1 |
| Bonasera, SJ; Boxer, AL; Cholfin, JA; Crawford, RK; Gennatas, ED; Gorno-Tempini, ML; Karydas, A; Kramer, JH; Miller, BL; Rankin, KP; Rosen, HJ; Sasaki, DA; Seeley, WW; Weiner, M; Zhou, J | 1 |
| Alberici, A; Archetti, S; Bianchi, M; Borroni, B; Cerini, C; Padovani, A; Paghera, B; Papetti, A; Premi, E | 1 |
3 other study(ies) available for valine and Frontotemporal Lobar Degeneration
| Article | Year |
|---|---|
Genetic contribution of FUS to frontotemporal lobar degeneration.
Topics: Aged; Amino Acid Sequence; Amyotrophic Lateral Sclerosis; DNA Mutational Analysis; DNA-Binding Proteins; Female; Frontotemporal Lobar Degeneration; Glycine; Humans; Male; Methionine; Middle Aged; Mutation, Missense; RNA-Binding Protein FUS; Sequence Alignment; Sequence Deletion; Valine | 2010 |
COMT Val158Met genotype influences neurodegeneration within dopamine-innervated brain structures.
Topics: Aged; Alleles; Alzheimer Disease; Catechol O-Methyltransferase; Cerebral Cortex; Dementia; Dopamine; Female; Frontotemporal Dementia; Frontotemporal Lobar Degeneration; Genotype; Humans; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Prefrontal Cortex; Valine | 2012 |
The brain-derived neurotrophic factor Val66Met polymorphism is associated with reduced hippocampus perfusion in frontotemporal lobar degeneration.
Topics: Aged; Aged, 80 and over; Brain-Derived Neurotrophic Factor; Female; Frontotemporal Lobar Degeneration; Hippocampus; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Valine | 2012 |