Tawil, Rabi

A phase I/IItrial of MYO‐029 in adult subjects with muscular dystrophy

Wagner, K. R., Fleckenstein, J. L., Amato, A. A., Barohn, R. J., Bushby, K., Escolar, D. M., Flanigan, K. M., Pestronk, A., Tawil, R., Wolfe, G. I., et al. (2008) · Annals of Neurology

Muscle Physiology and DisordersNeurogenetic and Muscular Disorders Research

Cited by 481

Facioscapulohumeral muscular dystrophy

Tawil, R., & Van Der Maarel, S. M. (2006) · Muscle & Nerve

Muscle Physiology and DisordersGenomics and Rare Diseases

Cited by 441

The primary periodic paralyses: diagnosis, pathogenesis and treatment

Venance, S. L., Cannon, S. C., Fialho, D., Fontaine, B., Hanna, M. G., Ptacek, L. J., Tristani-Firouzi, M., Tawil, R., & Griggs, R. C. (2006) · Brain

Ion channel regulation and functionCardiac electrophysiology and arrhythmias

Cited by 370

Evidence-based guideline summary: Evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine

Tawil, R., Kissel, J. T., Heatwole, C., Pandya, S., Gronseth, G., & Benatar, M. (2015) · Neurology

Muscle Physiology and DisordersNeurogenetic and Muscular Disorders Research

Cited by 234

Sex-Related Differences in Gene Expression in Human Skeletal Muscle

Welle, S., Tawil, R., & Thornton, C. A. (2008) · PLoS ONE

Muscle Physiology and DisordersGenetics and Physical Performance

Cited by 224

Facioscapulohumeral muscular dystrophy and DUX4: breaking the silence

van der Maarel, S. M., Tawil, R., & Tapscott, S. J. (2011) · Trends in Molecular Medicine

Muscle Physiology and DisordersGenomic variations and chromosomal abnormalities

Cited by 155

Facioscapulohumeral Muscular Dystrophy

Statland, J. M., & Tawil, R. (2016) · Continuum

Muscle Physiology and DisordersGenomics and Rare Diseases

Cited by 121

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

Facioscapulohumeral Dystrophy

Pandya, S., King, W. M., & Tawil, R. (2008) · Physical Therapy

Muscle Physiology and DisordersGenomics and Rare Diseases

Cited by 76

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

Patient‐identified disease burden in facioscapulohumeral muscular dystrophy

Johnson, N. E., Quinn, C., Eastwood, E., Tawil, R., & Heatwole, C. R. (2012) · Muscle & Nerve

Muscle Physiology and DisordersNeurogenetic and Muscular Disorders Research

Cited by 65