Neuromuscular Disorders in Children and Adolescents

Significant scientific and therapeutic advances have been made in recent decades, particularly in hereditary but also in acquired neuromuscular diseases. As a result of our increasing etiological understanding, the classification of these diseases has changed from a clinical–descriptive and formal–g...

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Format:	Online
Sprache:	Englisch
Veröffentlicht:	MDPI - Multidisciplinary Digital Publishing Institute 2022
Schlagworte:	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 thema EDItEUR::M Medicine and Nursing thema EDItEUR::M Medicine and Nursing::MK Medical specialties, branches of medicine::MKJ Neurology and clinical neurophysiology
Online-Zugang:	ONIX_20220506_9783036540702_128
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Neuromuscular Disorders in Children and Adolescents

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