SE-ATLAS

Genetic neuromuscular junction disease Acquired neuromuscular junction disease Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens Myotonia fluctuans Autosomal dominant proximal spinal muscular atrophy Neurogenic scapuloperoneal syndrome, Kaeser type Periodic paralysis with transient compartment-like syndrome Andersen-Tawil syndrome Neuromuscular disease Poliomyelitis Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Potassium-aggravated myotonia Bulbospinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Proximal spinal muscular atrophy Postpoliomyelitis syndrome Monomelic amyotrophy Primary lateral sclerosis Madras motor neuron disease Amyotrophic lateral sclerosis type 4 Atrophie musculaire progressive Sclérose latérale amyotrophique Canalopathie musculaire Syndrome d'Isaacs Amyotrophie spinale scapulopéronière Sclérose latérale amyotrophique juvénile Syndrome de Morvan Maladie du muscle squelettique Syndrome d'amyotrophie spinale proximale-épilepsie myoclonique progressive Maladie génétique du muscle squelettique Paralysie périodique hypokaliémique Paralysie périodique hyperkaliémique Paramyotonie d'Eulenburg Neuropathie motrice distale héréditaire Maladie acquise du muscle squelettique Maladie de la jonction neuromusculaire