Genome sequencing project finds answers for 25% of rare disease patients in a study
Some patients with a suspected rare genetic disease go without a diagnosis for years or even throughout a lifetime....
Some patients with a suspected rare genetic disease go without a diagnosis for years or even throughout a lifetime....
Research in different areas of therapy for various diseases has led to a wide range of treatments. Various diseases...
New research on oncology is creating new knowledge in several areas of therapy. This year is characterized by the...
Why do we make a fuss about rare mutations in NSCLC? In 2015, they only made up about 1-2%...
Nonalcoholic steatohepatitis (NASH) is an often silent but dangerous liver disease that affects an estimated 2% to 5% of...
Phage therapy – the treatment of bacterial infections with viruses that attack those bacteria – was used in the...
AL amyloidosis causes devastating symptoms and typically carries a poor prognosis, with a high risk of organ damage and...
Congenital athymia is a rare condition in which babies are born without a thymus. As a result, the immune...
New research shows the global prevalence of obesity and its contribution to the pathogenesis of polycystic ovary syndrome (PCOS)....
Hematological cancers were among the first to be discovered to have abnormal demethylation status. Excretion of epigenetic DNA modification...