Page last updated: 2024-08-23

tramadol and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

tramadol has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fu, J; Lv, H; Meng, L; Wang, Z; Yuan, Y; Zhang, W1

Other Studies

1 other study(ies) available for tramadol and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

ArticleYear
Novel mutations in HINT1 gene cause autosomal recessive axonal neuropathy with neuromyotonia in two cases of sensorimotor neuropathy and one case of motor neuropathy.
    Neuromuscular disorders : NMD, 2018, Volume: 28, Issue:8

    Topics: Adult; Female; Genotype; Hereditary Sensory and Motor Neuropathy; Humans; Isaacs Syndrome; Male; Muscle Weakness; Mutation; Nerve Tissue Proteins; Tramadol

2018