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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...

Täydet tiedot

Tallennettuna:
Aineistotyyppi: Online
Kieli:englanti
Julkaistu: MDPI - Multidisciplinary Digital Publishing Institute 2022
Aiheet:
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
Linkit:ONIX_20220506_9783036540702_128
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