Martens, William B.
Virginia Commonwealth University · University of Rochester Medicine
2 papers on CoChatORCID 0009-0006-6261-3701
Most cited papers
- Verified
Patient-Reported Symptoms in Facioscapulohumeral Muscular Dystrophy (PRISM-FSHD)
Hamel, J., Johnson, N., Tawil, R., Martens, W. B., Dilek, N., McDermott, M. P., & Heatwole, C. (2019) · Neurology
Muscle Physiology and DisordersNeurogenetic and Muscular Disorders Research
Cited by 88
- Verified
High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2
Hilbert, J. E., Barohn, R. J., Clemens, P. R., Luebbe, E. A., Martens, W. B., McDermott, M. P., Parkhill, A. L., Tawil, R., Thornton, C. A., Moxley, R. T., et al. (2017) · Neurology
Genetic Neurodegenerative DiseasesGastrointestinal motility and disorders
Cited by 70
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