| human | Q5 |
| P11496 | CiNii Research ID | 1420564276165188480 |
| P9776 | e-Rad researcher number | 60433025 |
| P7783 | J-GLOBAL ID | 201201051516159941 |
| P3835 | Mendeley person ID | en-kimura |
| P496 | ORCID iD | 0000-0002-7865-5918 |
| P3829 | Publons author ID | 2842779 |
| P1053 | ResearcherID | B-3869-2010 |
| E-3835-2017 | ||
| P5029 | Researchmap ID | enkimura |
| P1153 | Scopus author ID | 7202704893 |
| P69 | educated at | University of Washington | Q219563 |
| Kumamoto University | Q1148782 | ||
| P108 | employer | Nagoya University | Q1191132 |
| Japan Agency for Medical Research and Development | Q23010232 | ||
| University of Washington School of Medicine | Q7896584 | ||
| National Center of Neurology and Psychiatry | Q11421298 | ||
| Osaka University | Q651233 | ||
| Kumamoto University | Q1148782 | ||
| P734 | family name | Kimura | Q20978130 |
| Kimura | Q20978130 | ||
| Kimura | Q20978130 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q40083328 | A comparative study of care practices for young boys with Duchenne muscular dystrophy between Japan and European countries: Implications of early diagnosis |
| Q45857200 | A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy |
| Q59876149 | A novel GJB1 frameshift mutation produces a transient CNS symptom of X-linked Charcot–Marie–Tooth disease |
| Q40619274 | A reversible lesion of the corpus callosum splenium with adult influenza-associated encephalitis/encephalopathy: a case report |
| Q39611159 | Abnormal spinal MRI findings in human T-cell lymphotrophic virus type I-associated myelopathy |
| Q40756445 | Adenovirus-mediated murine interferon-gamma receptor transfer enhances the efficacy of IFN-gamma in vivo |
| Q48165000 | Amyotrophic lateral sclerosis in a patient with Kartagener syndrome |
| Q34530620 | An adult norovirus-related encephalitis/encephalopathy with mild clinical manifestation |
| Q43662965 | Bcl-2 expression by retrograde transport of adenoviral vectors with Cre-loxP recombination system in motor neurons of mutant SOD1 transgenic mice. |
| Q36953163 | Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy |
| Q34018494 | Cerebral amyloid angiopathy-related inflammation presenting with steroid-responsive higher brain dysfunction: case report and review of the literature |
| Q48165517 | Cervical MRI of subacute myelo-optico-neuropathy |
| Q36803129 | Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy). |
| Q55475347 | Characteristics of Japanese Patients with Becker Muscular Dystrophy and Intermediate Muscular Dystrophy in a Japanese National Registry of Muscular Dystrophy (Remudy): Heterogeneity and Clinical Variation. |
| Q45874288 | Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database. |
| Q36073309 | Clinical trial network for the promotion of clinical research for rare diseases in Japan: muscular dystrophy clinical trial network |
| Q51763687 | Comparison of the added value of contrast-enhanced 3D fluid-attenuated inversion recovery and magnetization-prepared rapid acquisition of gradient echo sequences in relation to conventional postcontrast T1-weighted images for the evaluation of lepto |
| Q38599411 | Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan |
| Q40646326 | Cre/loxP-mediated adenovirus type 5 packaging signal excision demonstrates that core element VI is sufficient for virus packaging |
| Q59876154 | DJ-1 forms complexes with mutant SOD1 and ameliorates its toxicity |
| Q39615787 | Derlin-1 overexpression ameliorates mutant SOD1-induced endoplasmic reticulum stress by reducing mutant SOD1 accumulation |
| Q47550338 | Detection and management of cardiomyopathy in female dystrophinopathy carriers |
| Q34526095 | Diffusion and ADC-map images detect ongoing demyelination on subcortical white matter in an adult metachromatic leukodystrophy patient with autoimmune Hashimoto thyroiditis |
| Q59876166 | Donor origin of multipotent adult progenitor cells in radiation chimeras |
| Q33730444 | Dystrophin delivery to muscles of mdx mice using lentiviral vectors leads to myogenic progenitor targeting and stable gene expression. |
| Q44469705 | Effective repetitive dystrophin gene transfer into skeletal muscle of adult mdx mice using a helper-dependent adenovirus vector expressing the coxsackievirus and adenovirus receptor (CAR) and dystrophin |
| Q27324593 | Efficient and reproducible myogenic differentiation from human iPS cells: prospects for modeling Miyoshi Myopathy in vitro |
| Q45877885 | Efficient repetitive gene delivery to skeletal muscle using recombinant adenovirus vector containing the Coxsackievirus and adenovirus receptor cDNA. |
| Q57160865 | Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease |
| Q55472596 | Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis. |
| Q57178737 | Female dystrophinopathy: Review of current literature |
| Q59876157 | Flexor-dominant myopathic phenotype in patients with His46Arg substitution in the Cu/Zn superoxide dismutase gene |
| Q59876169 | Full-length dystrophin cDNA transfer into skeletal muscle of adultmdx mice by electroporation |
| Q39611585 | Fulminant myelopathy following neurogenic proximal weakness associated with human T-cell lymphotropic virus type I infection |
| Q59876136 | Heatstroke in patients with Parkinson’s disease |
| Q59876141 | Long-Term Outcome of Polymyositis Treated with High Single-Dose Alternate-Day Prednisolone Therapy |
| Q59876160 | Mdx respiratory impairment following fibrosis of the diaphragm |
| Q59876124 | Medical Attitudes Survey for Female Dystrophinopathy Carriers in Japan |
| Q37400774 | Multicenter questionnaire survey for sporadic inclusion body myositis in Japan |
| Q43462570 | Muscle biopsy findings predictive of malignancy in rare infiltrative dermatomyositis |
| Q34698722 | Muscle fiber type-predominant promoter activity in lentiviral-mediated transgenic mouse |
| Q59876127 | Muscle-dominant wild-type TDP-43 expression induces myopathological changes featuring tubular aggregates and TDP-43-positive inclusions |
| Q43899664 | Myasthenic crisis patients who require intensive care unit management |
| Q59876129 | National registry of patients with Fukuyama congenital muscular dystrophy in Japan |
| Q33418112 | Nationwide patient registry for GNE myopathy in Japan |
| Q59876134 | Optineurin is potentially associated with TDP-43 and involved in the pathogenesis of inclusion body myositis |
| Q37349765 | Prednisolone improves walking in Japanese Duchenne muscular dystrophy patients |
| Q39996791 | Regions downstream from the WW domain of dystrophin are important for binding to postsynaptic densities in the brain |
| Q35086118 | Rescue from respiratory dysfunction by transduction of full-length dystrophin to diaphragm via the peritoneal cavity in utrophin/dystrophin double knockout mice |
| Q51620573 | Respiratory and cardiac function in japanese patients with dysferlinopathy. |
| Q50528721 | Serum Osteopontin as a Novel Biomarker for Muscle Regeneration in Duchenne Muscular Dystrophy. |
| Q59876144 | Significant CMAP decrement by repetitive nerve stimulation is more frequent in median than ulnar nerves of patients with amyotrophic lateral sclerosis |
| Q47202784 | Social involvement issues in patients with Becker muscular dystrophy: A questionnaire survey of subjects from a patient registry |
| Q45881869 | Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophin |
| Q38779576 | Study of Duchenne muscular dystrophy long-term survivors aged 40 years and older living in specialized institutions in Japan |
| Q42951107 | Successful treatment with rituximab and thalidomide of POEMS syndrome associated with Waldenstrom macroglobulinemia. |
| Q39744924 | Survey on genetic counseling and health management for symptomatic and asymptomatic female dystrophinopathy carriers in Japan today |
| Q35508913 | The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations |
| Q38406108 | The TREAT-NMD Duchenne muscular dystrophy registries: conception, design, and utilization by industry and academia |
| Q59876147 | The association between dermatomyositis and papillary thyroid cancer: a case report |
| Q50062082 | Tongue strength in patients with subacute myelo-optico-neuropathy. |
| Q59876164 | Transduction of Full-length Dystrophin to Multiple Skeletal Muscles Improves Motor Performance and Life Span in Utrophin/Dystrophin Double Knockout Mice |
| Q59876172 | Treatment of a Japanese Patient with Familial Amyloidotic Polyneuropathy with Orthotopic Liver Transplantation |
| Q37420460 | Trends in steroid therapy for Duchenne muscular dystrophy in Japan |
| Q48570790 | Tumefactive multiple sclerosis |
| Q40139753 | Usefulness of intraventricular infusion of antifungal drugs through Ommaya reservoirs for cryptococcal meningitis treatment. |
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