SE-ATLAS

Malignant hyperthermia of anesthesia Neuromuscular junction disease Genetic neuromuscular junction disease Acquired neuromuscular junction disease Motor neuron disease Myotonia fluctuans Acquired motor neuron disease Periodic paralysis with transient compartment-like syndrome Genetic motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens Neurogenic scapuloperoneal syndrome, Kaeser type Autosomal dominant proximal spinal muscular atrophy Andersen-Tawil syndrome Neuromuscular disease Juvenile primary lateral sclerosis Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Muskelatrophie, bulbospinale Myotonie, Kalium-sensitive Myotonia congenita Typ Thomsen und Becker Spinale Muskelatrophie, proximale Lateralsklerose, primäre Progressive Muskelatrophie Amyotrophe Lateralsklerose Typ 4 Motoneuron-Krankheit Madras Muskelatrophie, scapuloperoneale spinale Amyotrophe Lateralsklerose Ionenkanalkrankheit, muskuläre Isaacs-Syndrom Morvan-Syndrom Skelettmuskel-Krankheit Spinale Muskelatrophie-progressive Myoklonusepilepsie-Syndrom Paralyse, hypokaliämische periodische Paralyse, hyperkaliämische periodische Neuropathie, distale hereditäre motorische Paramyotonia congenita Eulenburg Amyotrophe Lateralsklerose, juvenile Genetisch bedingte Krankheit der Skelettmuskeln Erworbene Krankheit der Skelettmuskeln