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Jan 2, 2024 · More than 20 years ago, URMC neurologist Charles Thornton, MD, and others uncovered how a genetic flaw–a trinucleotide repeat expansion that results in thousands of repetitions of code on a segment of chromosome 19–gives rise to DM1.
Jun 20, 2024 · Charles Thornton, M.D. | Myotonic Dystrophy Foundation. Board Member. Dr. Thornton is Professor of Neurology at the University of Rochester. He, along with Dr. Moxley, is a Co-Director of the MDA clinic at URMC. He received his BA and medical degree from the University of Iowa.
Charles Donald Thornton, 80, of New Maryland, New Brunswick, passed away September 10th, 2022, after a long and valiant battle with cancer. Charles was born in Perth, Ontario, to Arthur William and Frances Barbara (Donald) Thornton.
Dr. Thornton's research program studies myotonic dystrophy, a common form of muscular dystrophy that begins in adulthood and is characterized by progressive muscle wasting and weakness. For this project, he focuses on myotonic dystrophy type 1 (DM1) which results from an unconventional RNA mutation.
Oct 23, 2023 · The underlying genetic cause of myotonic dystrophy type 1 (DM1), a trinucleotide repeat expansion located on chromosome 19, was discovered in 1992.
Nov 8, 2013 · Clipping found in The Akron Beacon Journal published in Akron, Ohio on 11/8/2013. Obituary for Charles B. Thornton (Aged 55)
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Jun 21, 2024 · DMCRN Members. The DMCRN is comprised of six medical centers with significant proficiency in myotonic dystrophy clinical care and research. The current DMCRN sites are: The University of Rochester is the lead DMCRN site, with Dr. Charles Thornton as the DMCRN PI.
