An infant with a fatal genetic disease has survived past the age of 2 with no signs of the condition, thanks to treatment ...

A two-and-a-half-year-old girl shows no signs of a rare genetic disorder, after becoming the first person to be treated for ...

Doctors diagnosed Carmen Lopez with spinal muscle atrophy (SMA) at birth, a rare genetic disorder that affects motor neurons ...

A toddler was successfully treated for a rare genetic disease, spinal muscular atrophy, after world-first in-womb therapy.

Johns Hopkins University School of Medicine researchers have discovered a dual regulatory mechanism safeguarding ...

Spinal muscle atrophyorspinal muscular atrophy(SMA) is a genetic disorder that can affect babies, children, and adults. A ...

A novel PET technique that visualizes spinal cord injuries provides critical information about which patients may be able to ...

This study demonstrates the critical role of Afadin on the generation and maintenance of complex cellular layers in the mouse retina. The data are solid, which provides important insights into how ...

Spinal cord compression (SCC) occurs in 5% to 30% of the oncology population and affects patient function, comfort, and general quality of life. Patients with lung cancer, breast cancer ...

Max Planck Institute for Biological Intelligence researchers have identified over 60 transcriptomic neuron types in the ...