melatonin has been researched along with Charcot-Marie-Tooth Disease in 1 studies
Charcot-Marie-Tooth Disease: A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)
| 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 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chahbouni, M | 1 |
| López, MDS | 1 |
| Molina-Carballo, A | 1 |
| de Haro, T | 1 |
| Muñoz-Hoyos, A | 1 |
| Fernández-Ortiz, M | 1 |
| Guerra-Librero, A | 1 |
| Acuña-Castroviejo, D | 1 |
1 other study available for melatonin and Charcot-Marie-Tooth Disease
| Article | Year |
|---|---|
Melatonin Treatment Reduces Oxidative Damage and Normalizes Plasma Pro-Inflammatory Cytokines in Patients Suffering from Charcot-Marie-Tooth Neuropathy: A Pilot Study in Three Children.
Topics: Charcot-Marie-Tooth Disease; Child; Cytokines; Glutathione; Glutathione Peroxidase; Humans; Interfer | 2017 |