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Vitamin E neuroprotection for cisplatin neuropathy: a randomized, placebo-controlled trial

Neurology, 2010-03, Vol.74 (9), p.762

2010

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Significance of multiple neurophysiological measures in patients with chronic disorders of consciousness

Clinical neurophysiology, 2015-03, Vol.126 (3), p.558-564

2015

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Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease

Neuromolecular medicine, 2006-03, Vol.8 (1-2), p.3-22

2006

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Four novel cases of periaxin-related neuropathy and review of the literature

Neurology, 2010-11, Vol.75 (20), p.1830

2010

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Marked phenotypic variability in two siblings with congenital myasthenic syndrome due to mutations in MUSK

Journal of neurology, 2013-11, Vol.260 (11), p.2894-2896

2013

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Sensory trick in task-specific tremor

Neurological sciences, 2017-07, Vol.38 (7), p.1341-1342

2017

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Giant SEPs and SEP-recovery function in Unverricht–Lundborg disease

Clinical neurophysiology, 2013-05, Vol.124 (5), p.1013-1018

2013

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Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease

Neurology, 2004-12, Vol.63 (12), p.2309

2004

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99. Auditory event-related potentials (ERPs) evoked by human syllables, musical notes/chords and animal sounds in pre-school children with specific expressive language disorders (SELDs) for assessing the selectiveness of auditory processing

Clinical neurophysiology, 2016-04, Vol.127 (4), p.e155-e155

2016

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109. Multicenter evaluation of somatosensory evoked potentials (SEPs) normative data in infancy

Clinical neurophysiology, 2013-11, Vol.124 (11), p.e213-e213

2013

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Electrophysiological evaluation of visual pathways in paclitaxel-treated patients

Journal of neuro-oncology, 2006-03, Vol.77 (1), p.79-87

2006

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P.12.4 Great phenotypic variability in two siblings affected by congenital myasthenic syndrome associated with mutations in MUSK

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.806-806

2013

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Event-related potential (ERP) markers of melodic processing: The N2 component is modulated by structural complexity, not by melodic ‘meaningfulness’

Brain research bulletin, 2010-08, Vol.83 (1), p.23-28

2010

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73. Acoustic neuroma surgery: Long term follow-up between facial nerve IOM monitored and non-monitored patients

Clinical neurophysiology, 2017-12, Vol.128 (12), p.e432-e432

2017

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15. Cortical median nerve somatosensory evoked potentials (cSEP) and cortical evoked high frequency oscillations (cHFO) in patients affected by hyperkinetic disorders and cortical increased-excitability

Clinical neurophysiology, 2017-12, Vol.128 (12), p.e418-e419

2017

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Movement-related desynchronization-synchronization (ERD/ERS) in patients with Unverricht–Lundborg disease

NeuroImage (Orlando, Fla.), 2006-10, Vol.33 (1), p.161-168

2006

Volltextzugriff (PDF)

Auditory ERPs and EEG abnormal findings in children with specific language impairment (SLI)

Clinical neurophysiology, 2019-01, Vol.130 (1), p.e7-e8

2019

Volltextzugriff (PDF)

P17.6 Asymmetrical functional topography of sensory and motor areas in a patient with motor and sensory impairment of the limbs

Clinical neurophysiology, 2011, Vol.122, p.S133-S133

2011

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Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II

Neurology, 2006-03, Vol.66 (5), p.748

2006

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P23-14 Action myoclonus in sialidosis: a comparative study with Unverricht-Lundborg disease

Clinical neurophysiology, 2010, Vol.121, p.S242-S242

2010

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P14-7 Somatosensory evoked potentials recovery function in patients with cortical myoclonus

Clinical neurophysiology, 2010, Vol.121, p.S186-S186

2010

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Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

Neurology, 1996-04, Vol.46 (4), p.1133

1996

Volltextzugriff (PDF)

Electroretinogram (ERGs) and visual evoked potentials (VEPs) study in prion disease (CJD)

Clinical neurophysiology, 2019-01, Vol.130 (1), p.e12-e13

2019

Volltextzugriff (PDF)

Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRI AA L and CMT-TRAUK): a double-blind randomised trial

Lancet neurology, 2011-04, Vol.10 (4), p.320-328

2011

Volltextzugriff (PDF)

Optic Nerve Disturbances: a New Form of Paclitaxel Neurotoxicity

JNCI : Journal of the National Cancer Institute, 1994-07, Vol.86 (14), p.1099-1101

1994

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Vitamin E neuroprotection for cisplatin neuropathy: a randomized, placebo-controlled trial

Significance of multiple neurophysiological measures in patients with chronic disorders of consciousness

Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease

Four novel cases of periaxin-related neuropathy and review of the literature

Marked phenotypic variability in two siblings with congenital myasthenic syndrome due to mutations in MUSK

Sensory trick in task-specific tremor

Giant SEPs and SEP-recovery function in Unverricht–Lundborg disease

Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease

99. Auditory event-related potentials (ERPs) evoked by human syllables, musical notes/chords and animal sounds in pre-school children with specific expressive language disorders (SELDs) for assessing the selectiveness of auditory processing

109. Multicenter evaluation of somatosensory evoked potentials (SEPs) normative data in infancy

Electrophysiological evaluation of visual pathways in paclitaxel-treated patients

P.12.4 Great phenotypic variability in two siblings affected by congenital myasthenic syndrome associated with mutations in MUSK

Event-related potential (ERP) markers of melodic processing: The N2 component is modulated by structural complexity, not by melodic ‘meaningfulness’

73. Acoustic neuroma surgery: Long term follow-up between facial nerve IOM monitored and non-monitored patients

15. Cortical median nerve somatosensory evoked potentials (cSEP) and cortical evoked high frequency oscillations (cHFO) in patients affected by hyperkinetic disorders and cortical increased-excitability

Movement-related desynchronization-synchronization (ERD/ERS) in patients with Unverricht–Lundborg disease

Auditory ERPs and EEG abnormal findings in children with specific language impairment (SLI)

P17.6 Asymmetrical functional topography of sensory and motor areas in a patient with motor and sensory impairment of the limbs

Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II

P23-14 Action myoclonus in sialidosis: a comparative study with Unverricht-Lundborg disease

P14-7 Somatosensory evoked potentials recovery function in patients with cortical myoclonus

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

Electroretinogram (ERGs) and visual evoked potentials (VEPs) study in prion disease (CJD)

Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRI AA L and CMT-TRAUK): a double-blind randomised trial

Optic Nerve Disturbances: a New Form of Paclitaxel Neurotoxicity

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