Imhoff, the team's Diabetes/Endocrinology, Kellogg Eye Center, Nephrology and Rheumatology communicator, joined Michigan Medicine in 2019. She's passionate about storytelling and brand activism.
When researchers study rare diseases, breakthroughs can be made that help patients. Revisit studies that are putting genetic puzzle pieces together to tackle these conditions.
A unique procedure, created by a Michigan Medicine pediatric surgeon, is repairing inguinal hernias in children using an ultrasound and a needle, with no incision needed.
A CALCR cell found in mice may stop feeding without subsequential nauseating effects as well as influence the long term intake of food.
A worldwide research effort is underway for finding a treatment option for hyperphagia, the most common genetic cause of life-threatening childhood obesity.
After sustaining a concussion, traditional treatment guidelines recommend strict rest, but a Michigan Medicine physician-researcher is challenging that concept with research that may advise otherwise.
Long hospital stays and invasive medical tests help identify serious bacterial infections in infants, but a U-M expert says there may be a more efficient, less painful way to make a diagnosis.
