SE-ATLAS

Sclérose latérale amyotrophique type 4 Syndrome de dystrophie musculaire-substance blanche cérébrale spongieuse Maladie du motoneurone type Madras Myopathie vacuolaire avec agrégation de protéines du réticulum sarcoplasmique Sclérose latérale amyotrophique Canalopathie musculaire Syndrome d'Isaacs Syndrome de Morvan Maladie du muscle squelettique Maladie génétique du muscle squelettique Paralysie périodique hypokaliémique Dystrophie musculaire Paralysie périodique hyperkaliémique Sclérose latérale amyotrophique juvénile Maladie acquise du muscle squelettique Paramyotonia congenita of Von Eulenburg Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Tel Hashomer camptodactyly syndrome Genetic neuromuscular junction disease Acquired neuromuscular junction disease Lambert-Eaton myasthenic syndrome Non-dystrophic myopathy Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Genetic periodic paralysis Autosomal dominant proximal spinal muscular atrophy Neurogenic scapuloperoneal syndrome, Kaeser type Myasthenia gravis Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Distal myopathy Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Infantile-onset ascending hereditary spastic paralysis Myotonic syndrome Potassium-aggravated myotonia Bulbospinal muscular atrophy Thomsen and Becker disease Proximal spinal muscular atrophy Periodic paralysis Muscular tumor Postpoliomyelitis syndrome Monomelic amyotrophy Infectious, fungal or parasitic myopathy Rippling muscle disease with myasthenia gravis Cyprus facial-neuromusculoskeletal syndrome Primary lateral sclerosis Idiopathic camptocormia