arginine has been researched along with Arterial Brain Diseases 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 |
|---|---|
| Kosakai, A; Nihonmatsu, M; Nishimoto, Y; Nishizawa, M; Nozaki, H; Onodera, O; Shibata, M; Shiga, A; Shirata, A; Suzuki, N; Takahashi, K; Yamane, K | 1 |
| Babinet, C; Cohen-Tannoudji, M; Domenga, V; Gridley, T; Joutel, A; Langa, F; Lemaire, B; Monet, M; Souilhol, C; Tournier-Lasserve, E | 1 |
2 other study(ies) available for arginine and Arterial Brain Diseases
| Article | Year |
|---|---|
A novel mutation in the HTRA1 gene causes CARASIL without alopecia.
Topics: Adult; Alopecia; Arginine; Base Sequence; Cerebral Infarction; Female; Glutamine; High-Temperature Requirement A Serine Peptidase 1; Humans; Intracranial Arterial Diseases; Leukoencephalopathy, Progressive Multifocal; Male; Mutation, Missense; Pedigree; Serine Endopeptidases | 2011 |
The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo.
Topics: Aging; Animals; Arginine; CADASIL; Cerebral Arteries; Cysteine; Immunoglobulin J Recombination Signal Sequence-Binding Protein; Intracranial Arterial Diseases; Lac Operon; Mice; Mice, Knockout; Mutant Proteins; Mutation, Missense; Protein Structure, Tertiary; Receptor, Notch3; Receptors, Notch; Transgenes | 2007 |