SE-ATLAS

Neurogenic scapuloperoneal syndrome, Kaeser type Botulism Autosomal dominant proximal spinal muscular atrophy Genetic periodic paralysis Congenital myasthenic syndrome Intellectual disability-developmental delay-contractures syndrome Periodic paralysis with transient compartment-like syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Juvenile primary lateral sclerosis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Potassium-aggravated myotonia Myotonic syndrome Thomsen and Becker disease Proximal spinal muscular atrophy Periodic paralysis Bulbospinal muscular atrophy Immune-mediated acquired neuromuscular junction disease Postpoliomyelitis syndrome Monomelic amyotrophy Muscular tumor Cyprus facial-neuromusculoskeletal syndrome Infectious, fungal or parasitic myopathy Primary lateral sclerosis Idiopathic camptocormia Muscular dystrophy-white matter spongiosis syndrome Progressive muscular atrophy Amyotrophic lateral sclerosis type 4 Idiopathic dropped head syndrome Madras motor neuron disease Scapuloperoneal spinal muscular atrophy Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Morvan syndrome Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Muscular dystrophy Hypokalemic periodic paralysis Skeletal muscle disease Neuropathie, distale hereditäre motorische Paralyse, hyperkaliämische periodische Paramyotonia congenita Eulenburg Genetisch bedingte Krankheit der Skelettmuskeln Amyotrophe Lateralsklerose, juvenile Erworbene Krankheit der Skelettmuskeln Myopathie, idiopathische inflammatorische Neuromuskuläre Übertragungsstörung Neuromuskuläre Übertragungsstörung, genetisch bedingte Tel-Hashomer-Kamptodaktylie-Syndrom Neuromuskuläre Übertragungsstörung, erworbene Myopathie, nichtdystrophe Motoneuronkrankheit Krankheit der Vorderhornzellen, autosomal-dominant oder rezessive Myotonia permanens Myotonia fluctuans Motoneuronkrankheit, erworbene Myotonia congenita, Azetazolamidempfindliche Vakuoläre Myopathie mit Proteinaggregaten des sarkoplasmatischen Retikulums