Neuromuscular Disorders in Children and Adolescents 

<br/><br/><br/>English[eng] 
<br/><br/><label>ISBN: </label>9783040000000 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Pompe disease||GAA gene||general population database||carrier frequency||genetic prevalence||spinal muscular atrophy||quality of life||child neurology||patient-reported outcomes||neuromuscular||carpal tunnel syndrome||median nerve neuropathy||electrodiagnostic studies||neuromuscular ultrasound||mucopolysaccharidosis||neuropathy||children||adolescents||Charcot–Marie–Tooth disease||traumatic neuropathy||inflammatory neuropathy||metabolic neuropathy||posterior spinal fusion||kyphosis||sagittal plane deformity||signal recognition particle||3-hydroxy-3-methylglutaryl||coenzyme A reductase||juvenile myositis||therapy||clinical course||chaperone-assisted autophagy||clinical trials||Duchenne muscular dystrophy||public health surveillance||distal arthrogryposis||AMC||ECEL1||contractures||muscle MRI||spinal muscular atrophy (SMA)||nusinersen||fine manual dexterity||ultrasonographic elastography||neuromuscular disease||muscle||brachial plexus neuritis||hereditary sensory and motor neuropathy||paralysis||vaccination||pediatrics||n/a