Search Results - "Wargon, I"
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Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations
Published in Neuromuscular disorders : NMD (01-04-2012)“…Abstract Congenital myasthenic syndromes (CMS) are clinically and genetically heterogeneous inherited disorders characterized by impaired neuromuscular…”
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A small deep infarct revealing leukoencephalopathy, calcifications and cysts in an adult patient
Published in Journal of neurology, neurosurgery and psychiatry (01-02-2008)“…[...]these data suggest that LCC belongs to the group of hereditary causes of ischaemic small-vessel diseases of the brain, which already include Cerebral…”
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The disynaptic group i inhibition between wrist flexor and extensor muscles revisited in humans
Published in Experimental brain research (01-01-2006)“…The present studies are designed to further characterise the interneuronal pathway mediating the disynaptic reciprocal group I inhibition between flexors and…”
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Post-activation depression in various group I spinal pathways in humans
Published in Experimental brain research (01-10-2005)“…This investigation was designed to study the effects of post-activation depression in different spinal pathways fed by group I afferents available to…”
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1.204 PILOT COMPARATIVE STUDY IN PSP AND FTD OF THE EFFECTS OF NEUROFEEDBACK IN COGNITIVE SYMPTOMS
Published in Parkinsonism & related disorders (2012)Get full text
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P5.17 Congenital Myasthenic Syndromes with COLQ mutations: Long term follow-up
Published in Neuromuscular disorders : NMD (01-10-2011)Get full text
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Evidence for recurrent inhibition of reciprocal inhibition from soleus to tibialis anterior in Man
Published in Experimental brain research (01-09-2003)“…Reciprocal inhibition between ankle flexors and extensors has been the subject of numerous studies in Man. They have demonstrated that this reciprocal…”
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P2.37 Long term prognosis of congenital myasthenic syndromes (CMS): The French CMS network experience
Published in Neuromuscular disorders : NMD (01-10-2010)Get full text
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Frequency and Phenotypes Associated with C9ORF72 Repeat Expansion in French FTLD and FTLD-ALS Patients (S54.003)
Published in Neurology (26-04-2012)“…Abstract only…”
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Caractéristiques cliniques et paracliniques d’un déficit en phosphoglucomutase (PGM)
Published in Revue neurologique (01-04-2014)Get full text
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The disynaptic group I inhibition between wrist flexor and extensor muscles revisited in humans
Published in Experimental brain research (01-01-2006)“…The present studies are designed to further characterise the interneuronal pathway mediating the disynaptic reciprocal group I inhibition between flexors and…”
Get full text
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3.6 Effects of vestibular galvanic stimulation onto variousmonosynaptic reflexes and presynaptic inhibition in humans
Published in Gait & posture (01-06-2005)Get full text
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Fréquence et phénotypes associés aux mutations du gène c9orf72 dans une cohorte française de patients atteints de DLFT
Published in Revue neurologique (01-04-2012)Get full text
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