<p>A) Representative MEPdia before vagotomy, after vagotomy and injection of a paralytic agent (gallamine trietiodide) obtained with the “Unshielded” coil. B) Representative MEPdia before vagotomy, after vagotomy and injection of a paralytic agent (gallamine trietiodide) obtained with the “Shielded” coil. Note that the vagotomy does not affect the MEPdia, and the paralytic agent abolish the MEPdia in both conditions in A and B. C) Histogram of the MEPdia amplitude before vagotomy, after vagotomy and following the injection of paralytic agent in the “Unshielded” (black histogram) and “Shielded” (White histogram) on the TMS coil. *: p<0.001.</p
In a 57-yr-old female with dystrophia myotonica, attempts to reverse residual non-depolanzmg block w...
Objective: Myotonia is caused by involuntary firing of skeletal muscle action potentials and causes ...
<p>The MMG-MEPs responses from FCR muscle during FCR voluntary contraction without median nerve stim...
<p>A) Representatives MEPdia (black arrows) obtained after a single TMS pulse at −6 mm from Bregma (...
THE phenomenon of myotonia consists of a delay in relaxation of voluntary muscle following upon a co...
Objective: To investigate the cause of transient weakness in myotonia congenita (MC) and the mechani...
A case of prolonged muscular paresis is reported following the administration of 120 mg of gallamine...
Digestive disorders following selective vagotomy and total vagotomy were compared in 2 groups of ani...
1 Neuromuscular (NM) changes resulting from organo-phosphate exposure are known to be complex. After...
Clinical nuerophysiological studies are presented of the effects of oral pyridostigmine bromide on n...
Objective: The aim of this study was to verify the action of Botulinum toxin type-A (BoNT-A) by mean...
Item does not contain fulltextPatients with autosomal recessive generalized myotonia, or Becker's di...
Patients with autosomal recessive generalized myotonia, or Pecker's disease, often suffer from a pec...
A survey of the reported responses of myotonic patients to depolarizing relaxants reveals the variab...
The two marjor properties to be considered are: - the degree of paralysis, which depends on the aff...
In a 57-yr-old female with dystrophia myotonica, attempts to reverse residual non-depolanzmg block w...
Objective: Myotonia is caused by involuntary firing of skeletal muscle action potentials and causes ...
<p>The MMG-MEPs responses from FCR muscle during FCR voluntary contraction without median nerve stim...
<p>A) Representatives MEPdia (black arrows) obtained after a single TMS pulse at −6 mm from Bregma (...
THE phenomenon of myotonia consists of a delay in relaxation of voluntary muscle following upon a co...
Objective: To investigate the cause of transient weakness in myotonia congenita (MC) and the mechani...
A case of prolonged muscular paresis is reported following the administration of 120 mg of gallamine...
Digestive disorders following selective vagotomy and total vagotomy were compared in 2 groups of ani...
1 Neuromuscular (NM) changes resulting from organo-phosphate exposure are known to be complex. After...
Clinical nuerophysiological studies are presented of the effects of oral pyridostigmine bromide on n...
Objective: The aim of this study was to verify the action of Botulinum toxin type-A (BoNT-A) by mean...
Item does not contain fulltextPatients with autosomal recessive generalized myotonia, or Becker's di...
Patients with autosomal recessive generalized myotonia, or Pecker's disease, often suffer from a pec...
A survey of the reported responses of myotonic patients to depolarizing relaxants reveals the variab...
The two marjor properties to be considered are: - the degree of paralysis, which depends on the aff...
In a 57-yr-old female with dystrophia myotonica, attempts to reverse residual non-depolanzmg block w...
Objective: Myotonia is caused by involuntary firing of skeletal muscle action potentials and causes ...
<p>The MMG-MEPs responses from FCR muscle during FCR voluntary contraction without median nerve stim...