Brian Tseng, M.D., Ph.D.

Neurology Massachusetts General Hospital & Harvard Medical School, Boston, MA, United States 
"Brian Tseng"
Mean distance: 17.86 (cluster 11)
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Torriani M, Townsend E, Thomas BJ, et al. (2012) Lower leg muscle involvement in Duchenne muscular dystrophy: an MR imaging and spectroscopy study. Skeletal Radiology. 41: 437-45
Bianchi ML, Biggar D, Bushby K, et al. (2011) Endocrine aspects of Duchenne muscular dystrophy. Neuromuscular Disorders : Nmd. 21: 298-303
Foley AR, Hu Y, Zou Y, et al. (2011) Large genomic deletions: a novel cause of Ullrich congenital muscular dystrophy. Annals of Neurology. 69: 206-11
Wang CH, Bonnemann CG, Rutkowski A, et al. (2010) Consensus statement on standard of care for congenital muscular dystrophies. Journal of Child Neurology. 25: 1559-81
Qureshi MM, McClure WC, Arevalo NL, et al. (2010) The Dietary Supplement Protandim Decreases Plasma Osteopontin and Improves Markers of Oxidative Stress in Muscular Dystrophy Mdx Mice. Journal of Dietary Supplements. 7: 159-178
Shenoy AM, Markowitz JA, Bonnemann CG, et al. (2010) Muscle-Eye-Brain disease. Journal of Clinical Neuromuscular Disease. 11: 124-6
Tseng B. (2010) Best practice in Duchenne muscular dystrophy. Neuromuscular Disorders : Nmd. 20: 217; author reply 21
Wakefield SE, Dimberg EL, Moore SA, et al. (2009) Dystrophinopathy presenting with arrhythmia in an asymptomatic 34-year-old man: a case report. Journal of Medical Case Reports. 3: 8625
Vandenburgh H, Shansky J, Benesch-Lee F, et al. (2009) Automated drug screening with contractile muscle tissue engineered from dystrophic myoblasts. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 23: 3325-34
McClure WC, Rabon RE, Ogawa H, et al. (2007) Upregulation of the creatine synthetic pathway in skeletal muscles of mature mdx mice. Neuromuscular Disorders : Nmd. 17: 639-50
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