nad has been researched along with Spastic Paraplegia, Hereditary 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 | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alavi, A; Ghasemi, A; Rohani, M; Sadr, Z | 1 |
| Barth, E; Evangelista, G; Langer, T; Molinié, T; Montoro-Gámez, C; Nolte, H; Popovic, M; Rugarli, EI; Trifunovic, A; Tröder, SE; Zevnik, B | 1 |
2 other study(ies) available for nad and Spastic Paraplegia, Hereditary
| Article | Year |
|---|---|
NMNAT1 and hereditary spastic paraplegia (HSP): expanding the phenotypic spectrum of NMNAT1 variants.
Topics: Humans; Leber Congenital Amaurosis; Mutation; NAD; Nicotinamide-Nucleotide Adenylyltransferase; Pedigree; Spastic Paraplegia, Hereditary | 2023 |
SARM1 deletion delays cerebellar but not spinal cord degeneration in an enhanced mouse model of SPG7 deficiency.
Topics: Animals; Armadillo Domain Proteins; ATPases Associated with Diverse Cellular Activities; Axons; Cerebellum; Cytoskeletal Proteins; Humans; Metalloendopeptidases; Mice; NAD; Spastic Paraplegia, Hereditary | 2023 |