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Degenerative Cervical Myelopathy and the Aging Spine
Degenerative Cervical Myelopathy and the Aging Spine
Autore Nouri Aria
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 electronic resource (184 p.)
Soggetto topico Medicine
Soggetto non controllato EQ-5D
PROMIS
spine
transformation
quality of life
patient outcomes
validation
degenerative cervical myelopathy
elderly
old age
outcomes
complications
mJOA
SF-36
cervical canal stenosis
cervical spine surgery
higher-aged patients
neurological outcome
mJOA Score
MCID
genetics
single nucleotide polymorphism
ossification posterior longitudinal ligament
severity
surgery
focus issue
update
cervical spondylotic myelopathy
compressive myelopathy
cervical spondylotic myelopathy (CSM)
prospective
multicenter
anterior
posterior
cervical alignment
kyphosis
spinopelvic parameter
laminoplasty
myelopathy
physical impairment
gait
locomotion
gait assessment
enhanced gait variability index
degenerative cervical myelopathy (DCM)
surgical outcome
MRI
DTI
FA
ADC
signal changes spinal canal
neurophysiology
SSEP
MEP
cervical myelopathy
spinal cord compression
rheumatoid arthritis (RA)
cranial settling (CS)
atlantoaxial subluxation (AAS)
atlantoaxial instability (AAI)
diffusion tensor imaging (DTI)
fractional anisotropy (FA)
cervical MRI
myelopathy hand
snake-eye
owl sign
Hirayama disease
introduction
spinal cord injury
spondylosis
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557789703321
Nouri Aria  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Neuromuscular Disorders in Children and Adolescents
Neuromuscular Disorders in Children and Adolescents
Autore Korinthenberg Rudolf
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (146 p.)
Soggetto topico Medicine
Neurology & clinical neurophysiology
Soggetto non controllato 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
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910566465903321
Korinthenberg Rudolf  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui