Spinal muscular atrophy: “Gene therapy is a real magic potion!”
Lucie was diagnosed with a rare neuromuscular disease four months after her birth: spinal muscular atrophy type 1. This pathology ...
Read moreLucie was diagnosed with a rare neuromuscular disease four months after her birth: spinal muscular atrophy type 1. This pathology ...
Read moreSpinal muscular atrophy is a rare, genetic and sometimes deadly disease. Depending on the type, it can affect fetuses, babies, ...
Read moreThe Swiss laboratory Novartis has announced that it will offer 100 randomly selected babies suffering from spinal muscular atrophy (SMA) ...
Read moreIntended for children with spinal muscular atrophy, Zolgensma has just obtained the green light from the authorities for marketing in ...
Read moreSpina bifida is a very serious fetal malformation. In the UK, the spines of two unborn babies with the condition ...
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