thymine has been researched along with Atrophy in 2 studies
Atrophy: Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Two families with frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) resulting from the microtubule associated protein tau (MAPT) gene IVS10+16C>T splice site mutation are reported, members of which showed variable clinical phenotypes at presentation." | 1.35 | Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation. ( Larner, AJ, 2009) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Larner, AJ | 1 |
| Assmann, BE | 1 |
| Van Kuilenburg, AB | 1 |
| Distelmaier, F | 1 |
| Abeling, NG | 1 |
| Rosenbaum, T | 1 |
| Schaper, J | 1 |
| Duran, M | 1 |
| Mayatepek, E | 1 |
2 other studies available for thymine and Atrophy
| Article | Year |
|---|---|
Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation.
Topics: Atrophy; Base Sequence; Brain; Brain Chemistry; Cytosine; Disease Progression; DNA; DNA Mutational A | 2009 |
Beta-ureidopropionase deficiency presenting with febrile status epilepticus.
Topics: Amidohydrolases; Atrophy; Central Nervous System Diseases; Diagnosis, Differential; Fever; Hematoma, | 2006 |