A new experimental treatment for children with a hard-to-treat form of epilepsy is safe and can reduce seizures dramatically, helping them lead much healthier and happier lives, the findings of a UCL ...
Spain has begun using a new genetic ALS therapy that targets the SOD1 mutation and may slow nerve damage in patients with this rare condition.
The FDA has granted Fast Track designation to AFTX-201 for the treatment of BAG3-associated dilated cardiomyopathy.
A team of researchers at Texas Children's Duncan Neurological Research Institute (NRI) and Baylor College of Medicine report ...
The origin of the nucleus remains hotly debated among scientists, but new imaging and genomic data are shedding light on this billion-year-old mystery.
A new experimental drug is showing remarkable promise for children with Dravet syndrome, a severe genetic form of epilepsy.
A team of researchers at Baylor College of Medicine and the Duncan Neurological Research Institute (Duncan NRI) at Texas ...
Post-traumatic stress disorder (PTSD) is not only characterized by strongly encoded traumatic memories, but also by disrupted coordination across brain networks. New research shows that treatment with ...
Proof-of-concept trial in a single patient shows that cells can survive transplantation without immunosuppression ...
A new gene-targeting strategy that boosts a crucial brain protein could pave the way for the first effective treatment for Rett syndrome. Researchers at Texas Children’s Duncan Neurological Research I ...
A new study discovers how nitric oxide triggers a biochemical domino effect in the brain, leading to mTOR overactivation in ...
A doctor who had a genetic condition that prevents teeth from forming searched for the DNA mutation that had affected his family for over 150 years.
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