thymidine 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 | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Stojkovic, T | 1 |
| Latour, P | 1 |
| Viet, G | 1 |
| de Seze, J | 1 |
| Hurtevent, JF | 1 |
| Vandenberghe, A | 1 |
| Vermersch, P | 1 |
1 other study available for thymidine and Charcot-Marie-Tooth Disease
| Article | Year |
|---|---|
Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene.
Topics: Adult; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; Electric Stimulation; Evoked Potentials | 2004 |