Connecting people

“ENMC: a real step forward in connecting people world-wide to make progress

in the treatment of patients with Neuromuscular Disorders”

Welcome to ENMC

Most neuromuscular disorders are rare (orphan) diseases, meaning that fewer than 1 in 2000 people are affected. They all cause a weakening of muscles, which could lead to tremendous disability. Because of this, international collaboration is extremely important to accelerate our knowledge and discovery of new medicines in the field of neuromuscular diseases.

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Submission deadline of workshop applications:

15 September 2019 

This is ENMC at a glance:

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Workshops Reports Patient Participation Young Scientist Program

ENMC Mission Statement

“The mission of ENMC is to encourage and facilitate communication and collaboration in the field of neuromuscular research with the aim of improving diagnosis and prognosis, finding effective treatments and optimising standards of care to improve the quality of life of people affected by neuromuscular disorders.”

Most recent news

Now published: The 2nd report of the 25th Anniversary ENMC workshop on the role of the neuromuscular patient in Shared-Decision-Making!

  Ambrosini et al. Orphanet Journal of Rare Diseases…
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Let’s celebrate, new ENMC website online!

On April 11th, the Executive Committee came together for their…
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ENMC bibliometric report published

The CWTS bibliometric report on ENMC workshop derived publications…
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Next workshop application deadline: 15 September 2019

ENMC workshop applications can be submitted the whole year through,…
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Publication on the impact of 25 years ENMC workshops

Proud at our publication in Neuromuscular Disorders on “The…
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