References of "Wang, François-Charles"
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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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