about
PDCD10 gene mutations in multiple cerebral cavernous malformationsSusceptibility to Guillain-Barré syndrome is associated to polymorphisms of CD1 genes.Natura non facit saltus in anti-ganglioside antibody-mediated neuropathies.Monospecific high-affinity and complement activating anti-GM1 antibodies are determinants in experimental axonal neuropathy.Asymptomatic spinal cord involvement in posterior reversible encephalopathy syndrome.Neuroprotective effect of cathodal transcranial direct current stimulation in a rat stroke model.The effects of prolonged cathodal direct current stimulation on the excitatory and inhibitory circuits of the ipsilateral and contralateral motor cortex.Capsular warning syndrome mimicking a jacksonian sensory march.Autoantibodies to neurofascin-186 and gliomedin in multifocal motor neuropathy.Glial fibrillary acidic protein in Guillain-Barré syndrome: Methodological issues.Polymorphism of CD1 and SH2D2A genes in inflammatory neuropathies.Antiganglioside antibodies are associated with axonal Guillain–Barré syndrome: A Japanese–Italian collaborative studyGuillain–Barré syndrome associated with normal or exaggerated tendon reflexesElectrodiagnosis of GBS subtypes by a single study: not yet the squaring of the circleElectrophysiological comparison between males and females in HNPPCortical origin of myoclonus in early stages of corticobasal degenerationInvolvement of sensory fibres in axonal subtypes of Guillain-Barre syndromeMotor and sensory conduction failure in overlap of Guillain–Barré and Miller Fisher syndrome: Two simultaneous casesPitfalls in electrodiagnosis of Guillain-Barre syndrome subtypesGlial fibrillary acidic protein as a marker of axonal damage in chronic neuropathiesAcute sensory ataxic neuropathy with antibodies to GD1b and GQ1b gangliosides and prompt recoverySusceptibility to chronic inflammatory demyelinating polyradiculoneuropathy is associated to polymorphic GA repeat in the SH2D2A genePersistent multifocal conduction block in vasculitic neuropathy with IgM anti-gangliosidesPolymorphisms of CD1 genes in chronic dysimmune neuropathies
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Francesca Notturno
@ast
Francesca Notturno
@en
Francesca Notturno
@es
Francesca Notturno
@nl
type
label
Francesca Notturno
@ast
Francesca Notturno
@en
Francesca Notturno
@es
Francesca Notturno
@nl
prefLabel
Francesca Notturno
@ast
Francesca Notturno
@en
Francesca Notturno
@es
Francesca Notturno
@nl
P106
P1153
14047284100
P31
P496
0000-0002-4191-6619