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Low-dose perampanel improves refractory cortical myoclonus by the dispersed and suppressed paroxysmal depolarization shifts in the sensorimotor cortex

Clinical neurophysiology, 2019-10, Vol.130 (10), p.1804-1812

2019

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A Biomarker for Benign Adult Familial Myoclonus Epilepsy: High‐Frequency Activities in Giant Somatosensory Evoked Potentials

Movement disorders, 2021-10, Vol.36 (10), p.2335-2345

2021

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A Role of Aging in the Progression of Cortical Excitability in Benign Adult Familial Myoclonus Epilepsy type 1 Patients

Movement disorders, 2021-10, Vol.36 (10), p.2446-2448

2021

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Clinical and imaging features of nonmotor onset seizure in poststroke epilepsy

Epilepsia (Copenhagen), 2022-08, Vol.63 (8), p.2068-2080

2022

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Is Generalized and Segmental Dystonia Accompanied by Impairments in the Dopaminergic System?

Frontiers in neurology, 2021-11, Vol.12, p.751434-751434

2021

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Clinical diagnostic criteria of benign adult familial myoclonus epilepsy type 1 are highly concordant with genetic testing

Neurology and clinical neuroscience, 2023-05, Vol.11 (3), p.140-145

2023

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Developing an Asymmetry Method for Detecting Postictal Hyperperfusion in Poststroke Epilepsy

Frontiers in neurology, 2022-07, Vol.13, p.877386-877386

2022

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Interictal epileptiform discharges as a predictive biomarker for recurrence of poststroke epilepsy

Brain communications, 2022-11, Vol.4 (6), p.fcac312-fcac312

2022

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Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy with a Novel NOTCH3 Cys323Trp Mutation Presenting Border-Zone Infarcts: A Case Report and Literature Review

Journal of stroke and cerebrovascular diseases, 2016-08, Vol.25 (8), p.e128-e130

2016

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Marked response to perampanel: A decade-long course of giant somatosensory evoked potentials in Unverricht-Lundborg disease

Clinical neurophysiology, 2021-10, Vol.132 (10), p.2329-2331

2021

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Redefined giant somatosensory evoked potentials: Evoked epileptic complexes of excitatory and inhibitory components

Clinical neurophysiology, 2024-08, Vol.164, p.119-129

2024

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Pallidal deep brain stimulation for patients with myoclonus-dystonia without SGCE mutations

Journal of neurology, 2024-06, Vol.271 (6), p.2948-2954

2024

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Focal tonic seizures with asymmetrical posturing could allow voluntary movements: A lesson to not be misled for a non‐epileptic event

Epileptic disorders, 2023-06, Vol.25 (3), p.416-421

2023

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Specific consistency score for rational selection of epilepsy resection surgery candidates

Epilepsia (Copenhagen), 2024-05, Vol.65 (5), p.1322-1332

2024

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Periodic discharges plus fast activity on electroencephalogram predict worse outcomes in poststroke epilepsy

Epilepsia (Copenhagen), 2023-12, Vol.64 (12), p.3279-3293

2023

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A new, sensitive biomarker for abnormal cortical excitability: Single trial based synchronization and desynchronization with cortical myoclonus

Journal of the neurological sciences, 2021-10, Vol.429, p.118549, Article 118549

2021

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O1-081 Pathophysiology of benign adult familial myoclonus epilepsy (BAFME) by means of principle component analysis of giant somatosensory evoked potentials (SEPs)

Clinical neurophysiology, 2020-10, Vol.131 (10), p.e261-e261

2020

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P-EP028. Low-dose perampanel improves refractory cortical myoclonus by the dispersed and suppressed paroxysmal depolarization shifts in the sensorimotor cortex

Clinical neurophysiology, 2021-08, Vol.132 (8), p.e86-e87

2021

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A super‐elderly autopsy case of benign adult familial myoclonus epilepsy with a heterozygous mutation

Epileptic disorders, 2023-02, Vol.25 (1), p.110-113

2023

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Homozygous 31 trinucleotide repeats in the SCA2 allele are pathogenic for cerebellar ataxia

Neurology. Genetics, 2018-12, Vol.4 (6), p.e283-e283

2018

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Diffuse lesions in the limbic system with short‐term memory loss in a patient with multiple sclerosis

Clinical & experimental neuroimmunology, 2018-03, Vol.9 (S1), p.56-59

2018

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Two cases of acute onset of focal cortical reflex myoclonus following acute aseptic meningoencephalitis with positive anti-glutamate receptor autoantibody

Rinsho shinkeigaku = Clinical neurology, 2014, Vol.54 (7), p.543

2014

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Two cases of acute onset of focal cortical reflex myoclonus following acute aseptic meningoencephalitis with positive anti-glutamate receptor autoantibody

Rinshō shinkeigaku, 2014, Vol.54 (7), p.543-549

2014

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Marked response to perampanel: A decade-long course of giant somatosensory evoked potentials in Unverricht-Lundborg disease

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2021, Vol.132 (10), p.2329-2331

2021

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Low-dose perampanel improves refractory cortical myoclonus by the dispersed and suppressed paroxysmal depolarization shifts in the sensorimotor cortex

A Biomarker for Benign Adult Familial Myoclonus Epilepsy: High‐Frequency Activities in Giant Somatosensory Evoked Potentials

A Role of Aging in the Progression of Cortical Excitability in Benign Adult Familial Myoclonus Epilepsy type 1 Patients

Clinical and imaging features of nonmotor onset seizure in poststroke epilepsy

Is Generalized and Segmental Dystonia Accompanied by Impairments in the Dopaminergic System?

Clinical diagnostic criteria of benign adult familial myoclonus epilepsy type 1 are highly concordant with genetic testing

Developing an Asymmetry Method for Detecting Postictal Hyperperfusion in Poststroke Epilepsy

Interictal epileptiform discharges as a predictive biomarker for recurrence of poststroke epilepsy

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy with a Novel NOTCH3 Cys323Trp Mutation Presenting Border-Zone Infarcts: A Case Report and Literature Review

Marked response to perampanel: A decade-long course of giant somatosensory evoked potentials in Unverricht-Lundborg disease

Redefined giant somatosensory evoked potentials: Evoked epileptic complexes of excitatory and inhibitory components

Pallidal deep brain stimulation for patients with myoclonus-dystonia without SGCE mutations

Focal tonic seizures with asymmetrical posturing could allow voluntary movements: A lesson to not be misled for a non‐epileptic event

Specific consistency score for rational selection of epilepsy resection surgery candidates

Periodic discharges plus fast activity on electroencephalogram predict worse outcomes in poststroke epilepsy

A new, sensitive biomarker for abnormal cortical excitability: Single trial based synchronization and desynchronization with cortical myoclonus

O1-081 Pathophysiology of benign adult familial myoclonus epilepsy (BAFME) by means of principle component analysis of giant somatosensory evoked potentials (SEPs)

P-EP028. Low-dose perampanel improves refractory cortical myoclonus by the dispersed and suppressed paroxysmal depolarization shifts in the sensorimotor cortex

A super‐elderly autopsy case of benign adult familial myoclonus epilepsy with a heterozygous mutation

Homozygous 31 trinucleotide repeats in the SCA2 allele are pathogenic for cerebellar ataxia

Diffuse lesions in the limbic system with short‐term memory loss in a patient with multiple sclerosis

Two cases of acute onset of focal cortical reflex myoclonus following acute aseptic meningoencephalitis with positive anti-glutamate receptor autoantibody

Two cases of acute onset of focal cortical reflex myoclonus following acute aseptic meningoencephalitis with positive anti-glutamate receptor autoantibody

Marked response to perampanel: A decade-long course of giant somatosensory evoked potentials in Unverricht-Lundborg disease

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