SE-ATLAS

Morvan syndrome Skeletal muscle disease Hypokalemic periodic paralysis Genetic skeletal muscle disease Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Juvenile amyotrophic lateral sclerosis Acquired skeletal muscle disease Malignant hyperthermia of anesthesia Neuromuscular junction disease Acquired neuromuscular junction disease Genetic neuromuscular junction disease Motor neuron disease Genetic motor neuron disease Myotonia fluctuans Acquired motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens Neurogenic scapuloperoneal syndrome, Kaeser type Spinale Muskelatrophie, proximale, autosomal-dominante Andersen-Tawil-Syndrom Poliomyelitis Neuromuskuläre Krankheit Lateralsklerose, juvenile primäre Spinale Muskelatrophie, infantile, X-chromosomale Myotonie, Kalium-sensitive Hereditäre Spastische Paralyse, aufsteigende, des frühen Kindesalters Myotonia congenita Typ Thomsen und Becker Muskelatrophie, bulbospinale Spinale Muskelatrophie, proximale Post-Poliomyelitis-Syndrom Amyotrophie, monomelische Lateralsklerose, primäre Motoneuron-Krankheit Madras Amyotrophe Lateralsklerose Typ 4 Ionenkanalkrankheit, muskuläre Amyotrophe Lateralsklerose Isaacs-Syndrom