University Hospital of Strasbourg – Neuromuscular Centre at Hautepierre Hospital

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Our Neuromuscular Center in Strasbourg is labeled National Rare Disease Center for Neuromuscular Disorders from 2005 and is composed of two teams:
– for adults (head: Dr Nadaj-Pakleza), attached to the Neurology Department,
– for children (head: Prof Laugel) attached to the Pediatric Department.
We provide a comprehensive care for children and adults with various types of neuromuscular disorders as spinal muscular atrophy, Steinert disease, myasthenia gravis, Duchenne and Becker muscular dystrophy, metabolic myopathies, limb-girdle muscular dystrophies, facio-scapulo-humeral myopathy, congenital myopathies, hereditary and dysimmune neuropathies.
Our Neuromuscular Center collaborates with several labeled research teams and is involved in many research projects (gene therapy in Duchenne muscular dystrophy and spinal muscular atrophy, clinical trials in myasthenia, mitochondrial disorders and Charcot-Marie-Tooth disease type 1A).

HCP representation

Location

Group membership

University Hospital of Strasbourg – Neuromuscular Centre at Hautepierre Hospital participates in the following groups…

Specialised Groups

Muscle diseases
Peripheral Nerve Disease
Motor Neuron Disease
Neuromuscular Junction Defects
Mitochondrial Diseases

Cross Cutting Specialised Groups

Neuromuscular Imaging
Neurophysiology
Neuromuscular Pathology
Genetics

University Hospital of Strasbourg – Neuromuscular Centre at Hautepierre Hospital is registered with the Care and Trial Site Registry

The ERNs are co-funded by the
European Union (Health Programme and CEF)

EU Commission


“EURO-NMD is one of the 24 European Reference Networks (ERNs) approved by the ERN Board of Member States. The ERNs are co-funded by the European Union (Health Programme and CEF).
For more information about the ERNs and the EU health strategy,
please visit ec.europa.eu/health/ern