nad has been researched along with CACH Syndrome 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 | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ashrafi, MR; Garshasbi, M; Heidari, M; Mahdieh, N; Mohammadi, P | 1 |
| Berlinguer-Palmini, R; Cavone, L; Chiarugi, A; Felici, R; Lapucci, A; Pratesi, S | 1 |
2 other study(ies) available for nad and CACH Syndrome
| Article | Year |
|---|---|
A novel homozygous missense variant in the NAXE gene in an Iranian family with progressive encephalopathy with brain edema and leukoencephalopathy.
Topics: Brain Edema; Child, Preschool; Humans; Infant; Iran; Lactates; Leukoencephalopathies; Male; Mutation, Missense; NAD; Pedigree; Racemases and Epimerases; Seizures | 2022 |
Pharmacological NAD-Boosting Strategies Improve Mitochondrial Homeostasis in Human Complex I-Mutant Fibroblasts.
Topics: Energy Metabolism; Fibroblasts; Homeostasis; Humans; Infant; Leukoencephalopathies; Membrane Potential, Mitochondrial; Mitochondria; Mutation; NAD; NADH Dehydrogenase; Niacinamide; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerase Inhibitors; Pyridinium Compounds; Signal Transduction | 2015 |