Family groups, researchers join forces to solve mysteries of autism gene
Families of children with mutations in a gene called SYNGAP1 have spurred research into the effects of the mutations on people — and how to treat them.
Families of children with mutations in a gene called SYNGAP1 have spurred research into the effects of the mutations on people — and how to treat them.
The ratio of autistic boys to girls is roughly the same among children with epilepsy, according to a new meta-analysis.
The signaling imbalance theory holds that the brains of autistic people are hyper-excitable because of either excess neuronal activity or weak brakes on that activity.
Una remota ciudad colombiana es el hogar del grupo más grande de personas con síndrome de X frágil. Los científicos están aprendiendo de ellos y tratando de ayudar.
Case reports suggest electroconvulsive therapy is effective for treating catatonia in people with autism.
Mice lacking one copy of a gene linked to autism are small and show striking changes in the number and quality of their cries.
A top autism gene called SCN2A plays a role at neuronal connections into adulthood, offering hope for treating mutations after infancy.
A remote Colombian town is home to the world’s largest cluster of people with fragile X syndrome. Scientists are learning from them — and trying to help.
The U.S. Drug Enforcement Agency has made it legal for doctors to prescribe an epilepsy drug derived from marijuana. But all other compounds derived from marijuana remain under tight restrictions.
A new brain implant pumps chemical signals directly into a target region to ease seizure-like activity in mice.