SE-ATLAS

Isaacs syndrome Morvan syndrome Skeletal muscle disease Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Hypokalemic periodic paralysis Steinert myotonic dystrophy Distal hereditary motor neuropathy Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Juvenile amyotrophic lateral sclerosis Genetic skeletal muscle disease Acquired skeletal muscle disease Myotonic dystrophy Neuromuscular junction disease Acquired neuromuscular junction disease Genetic neuromuscular junction disease Genetic motor neuron disease Periodic paralysis with transient compartment-like syndrome Neurogenic scapuloperoneal syndrome, Kaeser type Autosomal dominant proximal spinal muscular atrophy Andersen-Tawil syndrome Poliomyelitis Neuromuscular disease Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Mitochondrial myopathy Infantile-onset ascending hereditary spastic paralysis Proximal myotonic myopathy Potassium-aggravated myotonia Bulbospinal muscular atrophy Myotonie congénitale de Thomsen et Becker Amyotrophie spinale proximale Syndrome post-poliomyélite Amyotrophie monomélique Sclérose latérale primitive Sclérose latérale amyotrophique type 4 Atrophie musculaire progressive Maladie du motoneurone type Madras Amyotrophie spinale scapulopéronière Sclérose latérale amyotrophique Canalopathie musculaire Maladie du motoneurone Maladie acquise du motoneurone