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Palabras clave – provistas por la editorial

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