Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.
J Neurol
; 264(8): 1655-1677, 2017 Aug.
Article
en En
| MEDLINE
| ID: mdl-28364294
Palabras clave
Autosomal dominant inheritance; Autosomal recessive inheritance; Axonal degeneration; CharcotMarieTooth disease; Compound muscle action potential; Demyelination; Electrophysiology; Intermediate CharcotMarieTooth disease; Motor conduction velocity; Nerve biopsy; OMIM; PRISMA statement; Proximal motor nerve conduction velocity; Systematic review; X-linked inheritance
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Enfermedad de Charcot-Marie-Tooth
Tipo de estudio:
Systematic_reviews
Límite:
Animals
/
Humans
Idioma:
En
Revista:
J Neurol
Año:
2017
Tipo del documento:
Article
País de afiliación:
España
Pais de publicación:
Alemania