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

Affiliations: 
Neurology Massachusetts General Hospital & Harvard Medical School, Boston, MA, United States 
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"Brian Tseng"
Mean distance: 17.86 (cluster 11)
 
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Publications

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Barghout V, DeMuro C, Price M, et al. (2015) Skeletal Muscle activity and Resource tool for sporadic Inclusion body Myositis (Smart-Sibm): Characterization of Resource Utilization and Financial Burden Experienced By Sibm Patients Value in Health. 18: A284-A285
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
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
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
Tseng BS, Zhao P, Pattison JS, et al. (2002) Regenerated mdx mouse skeletal muscle shows differential mRNA expression. Journal of Applied Physiology (Bethesda, Md. : 1985). 93: 537-45
Tseng BS, Cavin ST, Booth FW, et al. (2000) Pulmonary hypoplasia in the myogenin null mouse embryo. American Journal of Respiratory Cell and Molecular Biology. 22: 304-15
Tseng BS, Cavin ST, Hoffman EP, et al. (1999) Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathies. Genomics. 57: 419-23
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