Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP).
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Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohortsClinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot StudyMultimodal MRI-based study in patients with SPG4 mutations.Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations.Upper motor neuron evaluation in multiple sclerosis patients treated with Sativex®
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Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP).
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 09 October 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Electrophysiological character ...... tary spastic paraplegia (HSP).
@en
Electrophysiological character ...... hereditary spastic paraplegia
@nl
type
label
Electrophysiological character ...... tary spastic paraplegia (HSP).
@en
Electrophysiological character ...... hereditary spastic paraplegia
@nl
prefLabel
Electrophysiological character ...... tary spastic paraplegia (HSP).
@en
Electrophysiological character ...... hereditary spastic paraplegia
@nl
P2093
P2860
P50
P356
P1476
Electrophysiological character ...... tary spastic paraplegia (HSP).
@en
P2093
Christian Frischholz
Kathrin N Karle
Stephan Klebe
Susanne Otto
P2860
P2888
P356
10.1186/1750-1172-8-158
P577
2013-10-09T00:00:00Z
P5875
P6179
1008972775