dapi has been researched along with Charcot-Marie-Tooth Disease in 1 studies
DAPI: RN given refers to parent cpd.
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 |
|---|---|
| Kabzińska, D | 1 |
| Kochański, A | 1 |
| Drac, H | 1 |
| Rowińska-Marcińska, K | 1 |
| Ryniewicz, B | 1 |
| Pedrola, L | 1 |
| Palau, F | 1 |
| Hausmanowa-Petrusewicz, I | 1 |
1 other study available for dapi and Charcot-Marie-Tooth Disease
| Article | Year |
|---|---|
A novel Met116Thr mutation in the GDAP1 gene in a Polish family with the axonal recessive Charcot-Marie-Tooth type 4 disease.
Topics: Adult; Animals; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Chlorocebus aethiops; COS Cell | 2006 |