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Author Details
Full Name
Yuko Shimizu
Affiliation
Tokyo Women's Medical University School of Medicine
ORCID
Career Start Year
1992
Papers
119
H Index
23
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36334134
Health-related quality of life in Japanese patients with multiple sclerosis.
J Neurol
2023
37560376
Studies of Health Insurance Claims Data in Japan: A Scoping Review.
JMA J
2023
37604479
Brain structural changes in alternating hemiplegia of childhood using single-case voxel-based morphometry analysis.
Int J Dev Neurosci
2023
37321879
Reply to letter to the editor "Regarding nusinersen and other therapeutic strategies for improved motor function".
Brain Dev
2023
37051222
Immunotherapy for ocular myasthenia gravis: an observational study in Japan.
Ther Adv Neurol Disord
2023
37326950
Systemic 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 Rep
2023
36508929
Characteristic cerebrospinal fluid findings in immune checkpoint inhibitor-related peripheral neuropathy: A case report.
J Neuroimmunol
2023
36460551
Muscle 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 Dev
2023
36631315
Skeletal anomaly and opisthotonus in early-onset epileptic encephalopathy with KCNQ2 abnormality.
Brain Dev
2023
34693484
Clinical and neuroimaging findings in patients with lissencephaly/subcortical band heterotopia spectrum: a magnetic resonance conventional and diffusion tensor study.
Neuroradiology
2022
35343426
Prolonged central motor conduction time and pyramidal tract degeneration in amyotrophic lateral sclerosis.
Clin Neuropathol
2022
35589488
Long-term changes in electroencephalogram findings in a girl with a nonsense SMC1A variant: A case report.
Brain Dev
2022
36210695
IgG4-related brain pseudotumor mimicking CNS lymphoma. A case report.
Neuropathology
2022
35972088
Volume-Based Radiofrequency Thermocoagulation for Pediatric Insulo-Opercular Epilepsy: A Feasibility Study.
Oper Neurosurg (Hagerstown)
2022
36305856
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy.
Genet Med
2022
34861614
Correlation of the symbol digit modalities test with the quality of life and depression in Japanese patients with multiple sclerosis.
Mult Scler Relat Disord
2022
35287025
Compassionate open-label use of rituximab following a randomised clinical trial against neuromyelitis optica (RIN-2 study): B cell monitoring-based administration.
Mult Scler Relat Disord
2022
32895939
ATP1A3 variants and slowly progressive cerebellar ataxia without paroxysmal or episodic symptoms in children.
Dev Med Child Neurol
2021
33678746
Diagnostic Utility of Polymerase Chain Reaction for Paraffin-embedded Sinus Specimens for Rhinocerebral Mucormycosis Complicated by Internal Carotid Artery Thrombosis and Cerebral Infarction.
Intern Med
2021
33762500
[Burnout in Japanese neurologists: comparison of male and female physicians].
Rinsho Shinkeigaku
2021
33504753
[Current and future strategies for burnout in Japanese neurologists].
Rinsho Shinkeigaku
2021
33610829
Highly sensitive screening of antisense sequences for different types of DMD mutations in patients' urine-derived cells.
J Neurol Sci
2021
34429366
Melanoma Cell Adhesion Molecule Expressing Helper T Cells in CNS Inflammatory Demyelinating Diseases.
Neurol Neuroimmunol Neuroinflamm
2021
34285095
Paraneoplastic AQP4-IgG-Seropositive Neuromyelitis Optica Spectrum Disorder Associated With Teratoma: A Case Report and Literature Review.
Neurol Neuroimmunol Neuroinflamm
2021
33189023
Hyperglycemic Crisis in Patients With Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS).
Pediatr Neurol
2021
33436735
HLA genotype-clinical phenotype correlations in multiple sclerosis and neuromyelitis optica spectrum disorders based on Japan MS/NMOSD Biobank data.
Sci Rep
2021
32873456
Postoperative improvement of executive function and adaptive behavior in children with intractable epilepsy.
Brain Dev
2021
32199095
Safety and efficacy of rituximab in neuromyelitis optica spectrum disorders (RIN-1 study): a multicentre, randomised, double-blind, placebo-controlled trial.
Lancet Neurol
2020
31725904
Renal dysfunction can occur in advanced-stage Duchenne muscular dystrophy.
Muscle Nerve
2020
31796239
Association of IgG4-Related Arteritis With Recurrent Stroke.
J Stroke Cerebrovasc Dis
2020
32034287
Publisher Correction: Modelling Duchenne muscular dystrophy in MYOD1-converted urine-derived cells treated with 3-deazaneplanocin A hydrochloride.
Sci Rep
2020
33232894
Association between lack of functional connectivity of the frontal brain region and poor response inhibition in children with frontal lobe epilepsy.
Epilepsy Behav
2020
32215054
Suitable indications of eculizumab for patients with refractory generalized myasthenia gravis.
Ther Adv Neurol Disord
2020
32173090
A case of CLCN2-related leukoencephalopathy with bright tree appearance during aseptic meningitis.
Brain Dev
2020
32320922
Adaptive behavior and its related factors in children with focal epilepsy.
Epilepsy Behav
2020
30621068
Restoring Dystrophin Expression in Duchenne Muscular Dystrophy: Current Status of Therapeutic Approaches.
J Pers Med
2019
31877123
Inhibition of FLT1 ameliorates muscular dystrophy phenotype by increased vasculature in a mouse model of Duchenne muscular dystrophy.
PLoS Genet
2019
31805047
Alteration of the anatomical covariance network after corpus callosotomy in pediatric intractable epilepsy.
PLoS One
2019
31469254
Childhood-onset cerebellar ataxia in Japan: A questionnaire-based survey.
Brain Behav
2019
31288946
Single-fiber electromyography-based diagnosis of CACNA1A mutation in children: A potential role of the electrodiagnosis in the era of whole exome sequencing.
Brain Dev
2019
31514443
Potential Therapies Using Myogenic Stem Cells Combined with Bio-Engineering Approaches for Treatment of Muscular Dystrophies.
Cells
2019
31370080
Static Leukoencephalopathy Associated with 17p13.3 Microdeletion Syndrome: A Case Report.
Neuropediatrics
2019
31124595
p.N345K mutation in TARDBP in a patient with familial amyotrophic lateral sclerosis: An autopsy case.
Neuropathology
2019
30798111
PD-1 inhibitor-associated severe myasthenia gravis with necrotizing myopathy and myocarditis.
J Neurol Sci
2019
30846748
Modelling Duchenne muscular dystrophy in MYOD1-converted urine-derived cells treated with 3-deazaneplanocin A hydrochloride.
Sci Rep
2019
30392831
Ischemic Stroke due to Virologically-Confirmed Varicella Zoster Virus Vasculopathy: A Case Series.
J Stroke Cerebrovasc Dis
2019
28657431
CSF and clinical data are useful in differentiating CNS inflammatory demyelinating disease from CNS lymphoma.
Mult Scler
2018
30237108
Proton magnetic resonance spectroscopy differentiates tumefactive demyelinating lesions from gliomas.
Mult Scler Relat Disord
2018
29907124
Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis.
Orphanet J Rare Dis
2018
30086429
Chronic sarcoid myopathy manifesting only as dysphagia and dysarthria in an 84-year-old woman.
Clin Neurol Neurosurg
2018
1 - 50 of 119
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Andrea Mora
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Adrianna Saada
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