References of "WANG, François-Charles"
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See detailLa neuropathie avec hypersensibilite hereditaire a la pression ou neuropathie tomaculaire
Tinant, France ULg; Zeevaert, Bernard ULg; Benkirane, H. et al

in Revue Médicale de Liège (2002), 57(10), 651-4

Hereditary neuropathy liability to pressure palsies is characterized by recurring accesses of painless paralysis at the level of various nerves likely to be compressed. This affection remains ... [more ▼]

Hereditary neuropathy liability to pressure palsies is characterized by recurring accesses of painless paralysis at the level of various nerves likely to be compressed. This affection remains underdiagnosed because of its usually benign course, sometimes without any symptom. The diagnosis is supported by clinical and electrophysiological data associated with, in the majority of patients, a deletion of one of the alleles coding for protein PMP 22 on the level of the locus 17p11.2. [less ▲]

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See detailEtude electromyographique paravertebrale dorso-lombaire. Analyse en mode multi-MUP et etablissement de normes au sein d'une population de reference
Tomasella, Marco ULg; Crielaard, Jean-Michel ULg; WANG, François-Charles ULg

in Neurophysiologie Clinique = Clinical Neurophysiology (2002), 32(2), 109-17

OBJECTIVE: The aim of this study was to contribute to draw up reference values relating to electromyographic (EMG) parameters in dorsal and lumbar paraspinal muscles. MATERIALS AND METHODS: 75 healthy ... [more ▼]

OBJECTIVE: The aim of this study was to contribute to draw up reference values relating to electromyographic (EMG) parameters in dorsal and lumbar paraspinal muscles. MATERIALS AND METHODS: 75 healthy subjects without back pain underwent electromyography of multifidus bundles, which are innervated uni-segmentally by the dorsal ram of the spinal nerve. T8, L3, L4, L5 and S1 myotomes were systematically explored. Output variables were spontaneous denervation activity and quantitative EMG data obtained by multi-MUP (Motor Unit action Potential) analysis. RESULTS: No abnormal insertional or spontaneous activity (such as fibrillation, positive sharp waves or fasciculation) was recorded at rest. Neither sex nor age influenced motor unit action potential features in our series. Reference values were drawn up for T8 and L5 segmental levels using the mean values of 20 motor unit potentials in each patient studied, the reference interval being defined by the lower and the upper outlier limits on individual values. CONCLUSION: This study offers reference data to electromyographers to help better identifying possible myogenic or neurogenic pathological changes, especially in lumbosacral radiculopathies. [less ▲]

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See detailCas clinique
WANG, François-Charles ULg

Scientific conference (2002, January 25)

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See detailExplorations neurophysiologiques des Myotonies
WANG, François-Charles ULg

Conference (2002)

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See detailValeurs de références de l’analyse en mode multi-MUP du multifidus dorso-lombaire
TOMASELLA, Marco ULg; CRIELAARD, Jean-Michel ULg; WANG, François-Charles ULg

in Neurophysiologie Clinique = Clinical Neurophysiology (2002)

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See detailAtteintes neuromusculaires aiguës de réanimation (ANMAR) : étude électrophysiologique prospective de 56 cas
BARTSCH, Valérie ULg; TOMASELLA, Marco ULg; Zeevaert, Bernard et al

in Neurophysiologie Clinique = Clinical Neurophysiology (2002)

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See detailLésion du nerf interosseux postérieur liée à une randonnée prolongée en vélo-tout-terrain (VTT)
Zeevaert, Bernard; CRIELAARD, Jean-Michel ULg; WANG, François-Charles ULg

in Neurophysiologie Clinique = Clinical Neurophysiology (2002)

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See detailSyndrome du canal lent associe a une translocation autosomique 2q31-9p27.
Zeevaert, Bernard ULg; Hansen, Isabelle ULg; Crielaard, Jean-Michel ULg et al

in Revue Neurologique (2002), 158(5 Pt 1), 605-8

A 27-year-old man complained of cervicoscapular and forearm weakness and amyotrophy. Electromyographic evaluation showed neuromuscular transmission dysfunction and a repetitive compound muscle action ... [more ▼]

A 27-year-old man complained of cervicoscapular and forearm weakness and amyotrophy. Electromyographic evaluation showed neuromuscular transmission dysfunction and a repetitive compound muscle action potential to a single stimulus. Prostigmine did not improve neuromuscular transmission. The genetic analysis of the patient's lymphocytes demonstrated a chromosomic 2q31-9p27 translocation. The combination of the clinical and electrophysiological data as well as the lack of auto-immunity signs against neuromuscular junction constituents led to the diagnosis to congenital postsynaptic myasthenic syndrome also called slow channel syndrome. This congenital myasthenic syndrome is for the first time associated with an autosomal translocation 2q31-9p27. [less ▲]

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See detailSymmetry of neurography
WANG, François-Charles ULg; Horward, A.

in Journal of Neurology (2002), 249

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