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Twins help progress and diagnosis of rare Myasthenia
Fourteen pairs of identical twins joined the EU funded medical project “ Fight-MG ”, to fight Myasthenia Gravis . This rare autoimmune disease leads to abnormal fatigability of various skeletal muscles.
New laser to watch DNA-proteins interactions
Within the framework of the European ATLAS project, a team of researchers in Naples has created a LASER-based prototype that could revolutionize medicine and our knowledge of the human genome .
New therapy against rare gene defects
European scientists set up new therapeutic approaches to tackle specific Lysosomal Storage Disorders: a new drug combination and enzyme replacement therapy against Pompe disease and gene therapy against MPS V I (Mucopolysaccharidosis VI).
Advances in Treating Huntington’s Disease
Juliet Ross is suffering from Huntington’s Disease, a rare neurological disorder that affects one in 10.000 people. Due to a genetic defect, her body produces a toxic protein that damages neurons in her brain .
The Fish that Protects Your Life
More than half of all deaths in Europe are caused by cardiovascular disease, and 80% of all these are due to atherosclerosis.
Stem Cells: A Genetic Perspective
Embryonic or neural stem cells are key tools for future studies on Parkinson’s disease or other degenerative diseases. So far, the only way to obtain embryonic stem cells implied the destruction of an embryo.
Calculating Fertility
We don’t really seem to know all that much about the organ we all come from.
The Secret of Sudden Death
Unlocking the mystery of that 5% of sudden cardiac deaths which are not caused by any apparent anatomic abnormality points to a group of inherited gene mutations in the heart’s ion channels.
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