Breakthrough Treatment Saves Newborn with Rare Genetic Mitochondrial Disease
Simple compound successfully treats life-threatening COQ2 deficiency in newborn, offering hope for rare mitochondrial disorders.
635 articles in this topic
Simple compound successfully treats life-threatening COQ2 deficiency in newborn, offering hope for rare mitochondrial disorders.
Large study reveals surprising protective gene variant may increase brain blood vessel damage under specific conditions.
Researchers combined ultrasound with gene therapy to treat Leigh syndrome, significantly extending survival in mouse models.
Scientists identify specific brain neurons that control withdrawal symptoms, opening new therapeutic pathways.
Scientists discover blocking UCHL3 enzyme reduces toxic protein clumps and improves cellular cleanup in Huntington's disease models.
Researchers discover autoimmune and acquired conditions can mimic Huntington's disease, affecting 2-40% of patients with similar symptoms.
New research maps the brain circuits behind creativity, offering insights into cognitive decline and potential preservation strategies.
Major review of 84,510 people identifies which sleep problems matter most for intervention and recovery strategies.
New research reveals PTSD patients show higher rates of REM sleep behavior disorder, potentially impacting long-term brain health.
New research reveals why human expertise remains crucial even as AI transforms sleep medicine diagnostics and treatment.
Researchers develop holistic NEST approach treating infant sleep issues through nurturing care rather than isolation methods.
Researchers develop a new tool to assess six key dimensions of circadian health and create a composite score for overall rhythm wellness.