SE-ATLAS

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