SE-ATLAS

Sclérose latérale primitive juvénile Myopathie distale Amyotrophie spinale infantile liée à l'X Paralysie spastique infantile ascendante héréditaire Syndrome myotonique Myotonie aggravée par le potassium Myotonie congénitale de Thomsen et Becker Amyotrophie bulbospinale de l'enfant Paralysie périodique Amyotrophie spinale proximale Amyotrophie bulbospinale Amyotrophie bulbospinale de l'adulte Syndrome post-poliomyélite Rippling muscle disease avec myasthenia gravis Amyotrophie spinale généralisée Amyotrophie monomélique Tumeur musculaire Myopathie infectieuse, fongique ou parasitaire Amyotrophie spinale proximale type 3 Syndrome neuro-musculo-squelettique type chypriote Amyotrophie spinale proximale type 2 Amyotrophie spinale proximale type 4 Sclérose latérale primitive Camptocormie idiopathique Autosomal dominant childhood-onset proximal spinal muscular atrophy Amyotrophic lateral sclerosis type 4 Lower motor neuron syndrome with late-adult onset Muscular dystrophy-white matter spongiosis syndrome Spinal muscular atrophy associated with central nervous system anomaly Autosomal dominant adult-onset proximal spinal muscular atrophy Madras motor neuron disease Autosomal dominant distal hereditary motor neuropathy Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Autosomal recessive distal hereditary motor neuropathy Muscular channelopathy Amyotrophic lateral sclerosis Isaacs syndrome Juvenile amyotrophic lateral sclerosis Proximal spinal muscular atrophy type 1 Morvan syndrome Muscular dystrophy Hypokalemic periodic paralysis Skeletal muscle disease Hyperkalemic periodic paralysis Genetic skeletal muscle disease Paramyotonia congenita of Von Eulenburg Idiopathic inflammatory myopathy Acquired skeletal muscle disease Malignant hyperthermia of anesthesia Neuromuscular junction disease Tel Hashomer camptodactyly syndrome Acquired neuromuscular junction disease Lambert-Eaton myasthenic syndrome Genetic neuromuscular junction disease Non-dystrophic myopathy X-linked distal spinal muscular atrophy type 3 Motor neuron disease Genetic motor neuron disease Myotonia permanens Myotonia fluctuans Acquired motor neuron disease Genetic periodic paralysis Acetazolamide-responsive myotonia Autosomal dominant proximal spinal muscular atrophy Neurogenic scapuloperoneal syndrome, Kaeser type Myasthenia gravis Intellectual disability-developmental delay-contractures syndrome Congenital myasthenic syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease