carnitine has been researched along with Deaf Mutism in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Carrozzo, R | 1 |
Dionisi-Vici, C | 1 |
Steuerwald, U | 1 |
Lucioli, S | 1 |
Deodato, F | 1 |
Di Giandomenico, S | 1 |
Bertini, E | 1 |
Franke, B | 1 |
Kluijtmans, LA | 1 |
Meschini, MC | 1 |
Rizzo, C | 1 |
Piemonte, F | 1 |
Rodenburg, R | 1 |
Santer, R | 1 |
Santorelli, FM | 1 |
van Rooij, A | 1 |
Vermunt-de Koning, D | 1 |
Morava, E | 1 |
Wevers, RA | 1 |
Silvestre-Aillaud, P | 1 |
BenDahan, D | 1 |
Paquis-Fluckinger, V | 1 |
Pouget, J | 1 |
Pelissier, JF | 1 |
Desnuelle, C | 1 |
Cozzone, PJ | 1 |
Vialettes, B | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Phase 2, Double-Blind, Placebo Controlled Clinical Trial of EPI-743 in Subjects With Cobalamin C Defect[NCT01793090] | Phase 2 | 30 participants (Actual) | Interventional | 2013-01-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
2 other studies available for carnitine and Deaf Mutism
Article | Year |
---|---|
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.
Topics: Atlantic Islands; Brain; Carnitine; Deafness; DNA Mutational Analysis; DNA, Mitochondrial; Family He | 2007 |
Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?
Topics: Blood Glucose; C-Peptide; Carnitine; Coenzymes; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondr | 1995 |