This section is dedicated specifically to researchers. You will find here the information about the opportunities of rare diseases research funding at the national level in  "National RD funding initiatives" and "Next generation sequencing facilities database" that groups sequencing platforms from Europe and Associated countires.

Vaincre les Maladies Lysosomales

The “Vaincre les Maladies Lysosomales” Society is regulated by the law of “1st July 1901”. It was created on 16 May 1990 by a group of parents of children suffering from lysosomal storage disorders. VML is recognized as being a public utility.

The actions of the Society follow three main themes:

  • Supporting Research in finding a Curative treatment
  • Supporting the Health Services in improving the patients’ quality of life
  • Supporting Families on a Daily basis

Title of the programme: Projets de recherche: Maladies Lysosomales
Type of the programme: thematic call for proposals. The VML Foundation fund basic and clinical scientific projects but also PhD fellowships.
Reccurence of the programme: yearly

E-Rare 2012 - Created by Toussaint Biger