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As the future of rare disease research at Cincinnati Children's is threatened, parents of 13-year-old Charlie Evans plead for its reinstatement.
FORT WORTH, Texas — An elderly white-haired gentlemen “with means,” who is a long time TCU benefactor and been around and around, recently said it best of this new era of college sports, “Now’s when ...
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Rare Hippo Grazing Near Riverbank with Zebra Nearby - MSN
African safari and wildlife expert Rob the Ranger reveals a rare hippo grazing peacefully along the riverbank at Zebra Plains River Camp.
Anthony Accetta has been embroiled in a battle over a 1930’s home with a colorful heritage that neighbors now call an eyesore. Two of his adjacent homes in a flood-prone area of the city have already ...
Ryan Lynch is seizing a second chance to travel and enjoy life after receiving a new FDA-approved treatment for his rare uveal melanoma.
Several new laws went into effect at the beginning of this month. One of them helps children, and their families, who are struggling with a very rare disease called Kleefstra syndrome.
Southern Indiana parents share daughter's battle with rare genetic disorder to raise awareness Willow had Citrullinemia, a rare genetic condition that prevents the body from properly removing ...
Two Alabama families are working together to fight for their children and raise awareness about a rare disease.
UW Health team restores eyesight to woman with rare disease MADISON (WKOW) -- UW Health is celebrating a new treatment that is helping a Wisconsin mom regain her vision after losing it three times.
Early research shows replacing brain immune cells slows a rare brain disease, with potential implications for treating Alzheimer’s and other neurodegenerative disorders.
Scientists have corrected gene mutations in mice causing an ultra-rare disease by editing DNA directly in the brain with a single injection, a feat with profound implications for patients with ...
Now for the first time in her life, Sallago is hopeful the world’s first cutting-edge gene-editing clinical trial for the rare genetic disease will potentially offer treatment for the disorder ...
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