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Author Details

Yuko Shimizu
Tokyo Women's Medical University School of Medicine
1992
119
23
PMIDPaper TitleJournal TitlePublished Year
36334134Health-related quality of life in Japanese patients with multiple sclerosis.J Neurol2023
37560376Studies of Health Insurance Claims Data in Japan: A Scoping Review.JMA J2023
37604479Brain structural changes in alternating hemiplegia of childhood using single-case voxel-based morphometry analysis.Int J Dev Neurosci2023
37321879Reply to letter to the editor "Regarding nusinersen and other therapeutic strategies for improved motor function".Brain Dev2023
37051222Immunotherapy for ocular myasthenia gravis: an observational study in Japan.Ther Adv Neurol Disord2023
37326950Systemic administration of the antisense oligonucleotide NS-089/NCNP-02 for skipping of exon 44 in patients with Duchenne muscular dystrophy: Study protocol for a phase I/II clinical trial.Neuropsychopharmacol Rep2023
36508929Characteristic cerebrospinal fluid findings in immune checkpoint inhibitor-related peripheral neuropathy: A case report.J Neuroimmunol2023
36460551Muscle impairment in MRI affect variability in treatment response to nusinersen in patients with spinal muscular atrophy type 2 and 3: A retrospective cohort study.Brain Dev2023
36631315Skeletal anomaly and opisthotonus in early-onset epileptic encephalopathy with KCNQ2 abnormality.Brain Dev2023
34693484Clinical and neuroimaging findings in patients with lissencephaly/subcortical band heterotopia spectrum: a magnetic resonance conventional and diffusion tensor study.Neuroradiology2022
35343426Prolonged central motor conduction time and pyramidal tract degeneration in amyotrophic lateral sclerosis.Clin Neuropathol2022
35589488Long-term changes in electroencephalogram findings in a girl with a nonsense SMC1A variant: A case report.Brain Dev2022
36210695IgG4-related brain pseudotumor mimicking CNS lymphoma. A case report.Neuropathology2022
35972088Volume-Based Radiofrequency Thermocoagulation for Pediatric Insulo-Opercular Epilepsy: A Feasibility Study.Oper Neurosurg (Hagerstown)2022
36305856Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy.Genet Med2022
34861614Correlation of the symbol digit modalities test with the quality of life and depression in Japanese patients with multiple sclerosis.Mult Scler Relat Disord2022
35287025Compassionate open-label use of rituximab following a randomised clinical trial against neuromyelitis optica (RIN-2 study): B cell monitoring-based administration.Mult Scler Relat Disord2022
32895939ATP1A3 variants and slowly progressive cerebellar ataxia without paroxysmal or episodic symptoms in children.Dev Med Child Neurol2021
33678746Diagnostic Utility of Polymerase Chain Reaction for Paraffin-embedded Sinus Specimens for Rhinocerebral Mucormycosis Complicated by Internal Carotid Artery Thrombosis and Cerebral Infarction.Intern Med2021
33762500[Burnout in Japanese neurologists: comparison of male and female physicians].Rinsho Shinkeigaku2021
33504753[Current and future strategies for burnout in Japanese neurologists].Rinsho Shinkeigaku2021
33610829Highly sensitive screening of antisense sequences for different types of DMD mutations in patients' urine-derived cells.J Neurol Sci2021
34429366Melanoma Cell Adhesion Molecule Expressing Helper T Cells in CNS Inflammatory Demyelinating Diseases.Neurol Neuroimmunol Neuroinflamm2021
34285095Paraneoplastic AQP4-IgG-Seropositive Neuromyelitis Optica Spectrum Disorder Associated With Teratoma: A Case Report and Literature Review.Neurol Neuroimmunol Neuroinflamm2021
33189023Hyperglycemic Crisis in Patients With Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS).Pediatr Neurol2021
33436735HLA genotype-clinical phenotype correlations in multiple sclerosis and neuromyelitis optica spectrum disorders based on Japan MS/NMOSD Biobank data.Sci Rep2021
32873456Postoperative improvement of executive function and adaptive behavior in children with intractable epilepsy.Brain Dev2021
32199095Safety and efficacy of rituximab in neuromyelitis optica spectrum disorders (RIN-1 study): a multicentre, randomised, double-blind, placebo-controlled trial.Lancet Neurol2020
31725904Renal dysfunction can occur in advanced-stage Duchenne muscular dystrophy.Muscle Nerve2020
31796239Association of IgG4-Related Arteritis With Recurrent Stroke.J Stroke Cerebrovasc Dis2020
32034287Publisher Correction: Modelling Duchenne muscular dystrophy in MYOD1-converted urine-derived cells treated with 3-deazaneplanocin A hydrochloride.Sci Rep2020
33232894Association between lack of functional connectivity of the frontal brain region and poor response inhibition in children with frontal lobe epilepsy.Epilepsy Behav2020
32215054Suitable indications of eculizumab for patients with refractory generalized myasthenia gravis.Ther Adv Neurol Disord2020
32173090A case of CLCN2-related leukoencephalopathy with bright tree appearance during aseptic meningitis.Brain Dev2020
32320922Adaptive behavior and its related factors in children with focal epilepsy.Epilepsy Behav2020
30621068Restoring Dystrophin Expression in Duchenne Muscular Dystrophy: Current Status of Therapeutic Approaches.J Pers Med2019
31877123Inhibition of FLT1 ameliorates muscular dystrophy phenotype by increased vasculature in a mouse model of Duchenne muscular dystrophy.PLoS Genet2019
31805047Alteration of the anatomical covariance network after corpus callosotomy in pediatric intractable epilepsy.PLoS One2019
31469254Childhood-onset cerebellar ataxia in Japan: A questionnaire-based survey.Brain Behav2019
31288946Single-fiber electromyography-based diagnosis of CACNA1A mutation in children: A potential role of the electrodiagnosis in the era of whole exome sequencing.Brain Dev2019
31514443Potential Therapies Using Myogenic Stem Cells Combined with Bio-Engineering Approaches for Treatment of Muscular Dystrophies.Cells2019
31370080Static Leukoencephalopathy Associated with 17p13.3 Microdeletion Syndrome: A Case Report.Neuropediatrics2019
31124595p.N345K mutation in TARDBP in a patient with familial amyotrophic lateral sclerosis: An autopsy case.Neuropathology2019
30798111PD-1 inhibitor-associated severe myasthenia gravis with necrotizing myopathy and myocarditis.J Neurol Sci2019
30846748Modelling Duchenne muscular dystrophy in MYOD1-converted urine-derived cells treated with 3-deazaneplanocin A hydrochloride.Sci Rep2019
30392831Ischemic Stroke due to Virologically-Confirmed Varicella Zoster Virus Vasculopathy: A Case Series.J Stroke Cerebrovasc Dis2019
28657431CSF and clinical data are useful in differentiating CNS inflammatory demyelinating disease from CNS lymphoma.Mult Scler2018
30237108Proton magnetic resonance spectroscopy differentiates tumefactive demyelinating lesions from gliomas.Mult Scler Relat Disord2018
29907124Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis.Orphanet J Rare Dis2018
30086429Chronic sarcoid myopathy manifesting only as dysphagia and dysarthria in an 84-year-old woman.Clin Neurol Neurosurg2018
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Collaborators

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Boston Children's Hospital
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Montreal Neurological Institute, McGill University
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Vanderbilt University Medical Center
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Center for Medical Genetics, Keio University School of Medicine
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