SE-ATLAS

Isaacs syndrome Morvan syndrome Skeletal muscle disease Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Hypokalemic periodic paralysis Distal hereditary motor neuropathy Steinert myotonic dystrophy Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Juvenile amyotrophic lateral sclerosis Genetic skeletal muscle disease Acquired skeletal muscle disease Malignant hyperthermia of anesthesia Myotonic dystrophy Neuromuscular junction disease Acquired neuromuscular junction disease Genetic neuromuscular junction disease Motor neuron disease Genetic motor neuron disease Periodic paralysis with transient compartment-like syndrome Acquired motor neuron disease 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 Mitochondriale Myopathie Hereditäre Spastische Paralyse, aufsteigende, des frühen Kindesalters Myopathie, myotone proximale Myotonie, Kalium-sensitive Muskelatrophie, bulbospinale Myotonia congenita Typ Thomsen und Becker Spinale Muskelatrophie, proximale Post-Poliomyelitis-Syndrom Amyotrophie, monomelische Lateralsklerose, primäre Amyotrophe Lateralsklerose Typ 4 Progressive Muskelatrophie Motoneuron-Krankheit Madras Muskelatrophie, scapuloperoneale spinale Amyotrophe Lateralsklerose Ionenkanalkrankheit, muskuläre