The AHA recommended whole exome or whole genome sequencing as first-line diagnostic tools for mitochondrial diseases.

Geneticists looking inside the nuclear genome for mutations that contribute to disease have long relied on a principal known as constraint modeling, which allows researchers to assess the degree of ...

Physical rehabilitation and symptom management still remain the mainstay of treatment for stroke, as clot removal or ...

A groundbreaking investigation from the Technical University of Munich has uncovered a crucial link between mitochondrial dysfunction and Crohn’s disease. This revelation could transform the ...

The UK’s pioneering licensed IVF technique to reduce the risk of mitochondrial diseases carried out in Newcastle has seen eight babies born, published research shows. All eight babies show no signs of ...

A finer glass tube and a more exacting technique with a refined procedure can reduce the likelihood of transmitting mitochondrial disease during assisted reproduction, according to new research. The ...

Study identifies plasma free-carnitine deficiency in women with aMCI and early-AD, highlighting mitochondrial metabolism as a target for individualized preventive treatments. Study: Sex differences in ...

MITOLINE™ Algorithm Powers Development of First-in-Class Small Molecules Targeting a Mitochondrial Carrier for Inflammatory ...

Prince Frederik of Luxembourg died at the age of 22 due to a rare mitochondrial condition called POLG disease—Newsweek has rounded up what you need to know about the illness. The European royal died ...