nad has been researched along with Child Mental Disorders 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 | 1 (33.33) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Christodoulou, J; Linster, CL; Van Bergen, NJ | 1 |
| Abe, J; Borna, NN; Furukawa, T; Fushimi, T; Imai-Okazaki, A; Kishita, Y; Murayama, K; Ogawa-Tominaga, M; Ohtake, A; Okazaki, Y; Takeda, A | 1 |
| Baldassarro, VA; Bergamini, C; Bianco, F; Bonora, E; Buscherini, F; Cordelli, DM; Diaz, R; Diquigiovanni, C; Fato, R; Liparulo, I; Masin, L; Paracchini, S; Pippucci, T; Rizzardi, N; Scarano, E; Seri, M; Tranchina, A; Wischmeijer, A | 1 |
3 other study(ies) available for nad and Child Mental Disorders
| Article | Year |
|---|---|
Reply: NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness.
Topics: Acute Disease; Humans; Hydro-Lyases; Mutation; NAD; Neurodegenerative Diseases; Neurodevelopmental Disorders | 2020 |
NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness.
Topics: Acute Disease; Humans; Hydro-Lyases; Mutation; NAD; Neurodegenerative Diseases; Neurodevelopmental Disorders | 2020 |
A novel mutation in
Topics: Calcium; Cell Cycle Proteins; Cell Line; Child; Electron Transport Complex I; Endosomes; Humans; Male; Mitochondria; Mitochondrial Diseases; Mutation; NAD; NADH Dehydrogenase; Neurodevelopmental Disorders; Pyruvates | 2019 |