Rare genetic variants linked to bicuspid aortic valve disease in young adults identified by UTHealth Houston researchers
Genetic variants linked to a rare form of bicuspid aortic valve disease that affects young adults and can lead to dangerous and potentially life-threatening aortic complications have been identified by researchers at UTHealth Houston. The study was published today in the American Journal…
AI and Genetic Diseases
McGovern Medical School research employs artificial intelligence to improve the diagnosis and treatment of hereditary conditions such as Marfan syndrome, Loeys-Dietz syndrome, and vascular Ehlers-Danlos syndrome.
Beta-blockers may help decrease bone loss in male patients with dementia, according to UTHealth Houston study
Men with dementia who were taking beta-blockers showed a slight decrease in the rate of bone loss compared with men who were not, according to a small observational study led by researchers at UTHealth Houston. Women in the study, published in Calcified Tissue…
In Memoriam: Dr. Barbara Murray
Barbara E. Murray, MD, J. Ralph Meadows Professor of Medicine in the Division of Infectious Diseases, Department of Internal Medicine, died April 11, 2024. She was 76. A member of the Medical School’s ID faculty since 1980, she was a…
Researchers uncover why a gene mutant causes young children to have strokes
A discovery of a mutation in the gene ACTA2 has given researchers, led by Dianna Milewicz, MD, PhD, with UTHealth Houston, insight into understanding the cause of a rare and progressive problem with arteries in the brain and a cause…
UTHealth Houston researcher awarded over $5M to study and improve the diagnostic process in clinics to prevent errors
Improving the diagnostic process and preventing errors are the focus of two studies funded by the U.S. Department of Health and Human Services (HHS) and led by Eric Thomas, MD, associate dean for health care quality with McGovern Medical School at UTHealth…