Lista de obras - En Kimura - Dominio Público Uruguay

A comparative study of care practices for young boys with Duchenne muscular dystrophy between Japan and European countries: Implications of early diagnosis

artículo científico publicado en 2017

A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy

artículo científico publicado en 2006

A novel GJB1 frameshift mutation produces a transient CNS symptom of X-linked Charcot–Marie–Tooth disease

artículo científico publicado en 2010

A reversible lesion of the corpus callosum splenium with adult influenza-associated encephalitis/encephalopathy: a case report

artículo científico publicado en 2008

Abnormal spinal MRI findings in human T-cell lymphotrophic virus type I-associated myelopathy

artículo científico publicado en 2009

Adenovirus-mediated murine interferon-gamma receptor transfer enhances the efficacy of IFN-gamma in vivo

artículo científico publicado en 2002

Amyotrophic lateral sclerosis in a patient with Kartagener syndrome

artículo científico publicado en 2010

An adult norovirus-related encephalitis/encephalopathy with mild clinical manifestation

artículo científico publicado en 2010

Bcl-2 expression by retrograde transport of adenoviral vectors with Cre-loxP recombination system in motor neurons of mutant SOD1 transgenic mice.

artículo científico publicado en 2001

Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy

artículo científico publicado en 2008

Cerebral amyloid angiopathy-related inflammation presenting with steroid-responsive higher brain dysfunction: case report and review of the literature

artículo científico publicado en 2011

Cervical MRI of subacute myelo-optico-neuropathy

artículo científico publicado en 2010

Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy).

artículo científico publicado en 2013

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.

artículo científico publicado en 2018

Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database.

artículo científico publicado en 2017

Clinical trial network for the promotion of clinical research for rare diseases in Japan: muscular dystrophy clinical trial network

artículo científico publicado en 2016

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

artículo científico publicado en 2009

Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan

artículo científico

Cre/loxP-mediated adenovirus type 5 packaging signal excision demonstrates that core element VI is sufficient for virus packaging

artículo científico publicado en 2003

DJ-1 forms complexes with mutant SOD1 and ameliorates its toxicity

article

Derlin-1 overexpression ameliorates mutant SOD1-induced endoplasmic reticulum stress by reducing mutant SOD1 accumulation

artículo científico publicado en 2010

Detection and management of cardiomyopathy in female dystrophinopathy carriers

artículo científico publicado en 2017

Diffusion and ADC-map images detect ongoing demyelination on subcortical white matter in an adult metachromatic leukodystrophy patient with autoimmune Hashimoto thyroiditis

artículo científico publicado en 2010

Donor origin of multipotent adult progenitor cells in radiation chimeras

scientific article published on 11 August 2005

Dystrophin delivery to muscles of mdx mice using lentiviral vectors leads to myogenic progenitor targeting and stable gene expression.

artículo científico publicado en 2009

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

artículo científico publicado en 2005

Efficient and reproducible myogenic differentiation from human iPS cells: prospects for modeling Miyoshi Myopathy in vitro

artículo científico publicado en 2013

Efficient repetitive gene delivery to skeletal muscle using recombinant adenovirus vector containing the Coxsackievirus and adenovirus receptor cDNA.

artículo científico publicado en 2001

Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis.

artículo científico publicado en 2018

Female dystrophinopathy: Review of current literature

article

Flexor-dominant myopathic phenotype in patients with His46Arg substitution in the Cu/Zn superoxide dismutase gene

article

Full-length dystrophin cDNA transfer into skeletal muscle of adultmdx mice by electroporation

artículo científico publicado en 2003

Fulminant myelopathy following neurogenic proximal weakness associated with human T-cell lymphotropic virus type I infection

artículo científico publicado en 2011

Heatstroke in patients with Parkinson’s disease

artículo científico publicado en 2011

Long-Term Outcome of Polymyositis Treated with High Single-Dose Alternate-Day Prednisolone Therapy

scientific article published on 11 July 2012

Mdx respiratory impairment following fibrosis of the diaphragm

artículo científico publicado en 2008

Medical Attitudes Survey for Female Dystrophinopathy Carriers in Japan

Multicenter questionnaire survey for sporadic inclusion body myositis in Japan

artículo científico publicado en 2016

Muscle biopsy findings predictive of malignancy in rare infiltrative dermatomyositis

artículo científico publicado en 2012

Muscle fiber type-predominant promoter activity in lentiviral-mediated transgenic mouse

artículo científico publicado en 2011

Muscle-dominant wild-type TDP-43 expression induces myopathological changes featuring tubular aggregates and TDP-43-positive inclusions

artículo científico publicado en 2018

Myasthenic crisis patients who require intensive care unit management

artículo científico publicado en 2012

National registry of patients with Fukuyama congenital muscular dystrophy in Japan

artículo científico publicado en 2018

Nationwide patient registry for GNE myopathy in Japan

artículo científico publicado en 2014

Optineurin is potentially associated with TDP-43 and involved in the pathogenesis of inclusion body myositis

scientific article published on 01 June 2013

Prednisolone improves walking in Japanese Duchenne muscular dystrophy patients

artículo científico publicado en 2013

Regions downstream from the WW domain of dystrophin are important for binding to postsynaptic densities in the brain

artículo científico publicado en 2008

Rescue from respiratory dysfunction by transduction of full-length dystrophin to diaphragm via the peritoneal cavity in utrophin/dystrophin double knockout mice

artículo científico publicado en 2011

Respiratory and cardiac function in japanese patients with dysferlinopathy

artículo científico publicado en 2015

Serum Osteopontin as a Novel Biomarker for Muscle Regeneration in Duchenne Muscular Dystrophy

artículo científico publicado en 2016

Significant CMAP decrement by repetitive nerve stimulation is more frequent in median than ulnar nerves of patients with amyotrophic lateral sclerosis

article

Social involvement issues in patients with Becker muscular dystrophy: A questionnaire survey of subjects from a patient registry

artículo científico publicado en 2017

Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophin

artículo científico publicado en 2005

Study of Duchenne muscular dystrophy long-term survivors aged 40 years and older living in specialized institutions in Japan

artículo científico publicado en 2016

Successful treatment with rituximab and thalidomide of POEMS syndrome associated with Waldenstrom macroglobulinemia.

artículo científico publicado en 2010

Survey on genetic counseling and health management for symptomatic and asymptomatic female dystrophinopathy carriers in Japan today

artículo científico publicado en 2016

The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations

artículo científico publicado en 2015

The TREAT-NMD Duchenne muscular dystrophy registries: conception, design, and utilization by industry and academia

artículo científico

The association between dermatomyositis and papillary thyroid cancer: a case report

scientific article published on 18 January 2011

Tongue strength in patients with subacute myelo-optico-neuropathy.

artículo científico publicado en 2017

Transduction of Full-length Dystrophin to Multiple Skeletal Muscles Improves Motor Performance and Life Span in Utrophin/Dystrophin Double Knockout Mice

Treatment of a Japanese Patient with Familial Amyloidotic Polyneuropathy with Orthotopic Liver Transplantation

artículo científico publicado en 1994

Trends in steroid therapy for Duchenne muscular dystrophy in Japan

artículo científico publicado en 2016

Tumefactive multiple sclerosis

artículo científico publicado en 2009

Usefulness of intraventricular infusion of antifungal drugs through Ommaya reservoirs for cryptococcal meningitis treatment.

artículo científico publicado en 2015

Lista de obras de En Kimura

A comparative study of care practices for young boys with Duchenne muscular dystrophy between Japan and European countries: Implications of early diagnosis

A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy

A novel GJB1 frameshift mutation produces a transient CNS symptom of X-linked Charcot–Marie–Tooth disease

A reversible lesion of the corpus callosum splenium with adult influenza-associated encephalitis/encephalopathy: a case report

Abnormal spinal MRI findings in human T-cell lymphotrophic virus type I-associated myelopathy

Adenovirus-mediated murine interferon-gamma receptor transfer enhances the efficacy of IFN-gamma in vivo

Amyotrophic lateral sclerosis in a patient with Kartagener syndrome

An adult norovirus-related encephalitis/encephalopathy with mild clinical manifestation

Bcl-2 expression by retrograde transport of adenoviral vectors with Cre-loxP recombination system in motor neurons of mutant SOD1 transgenic mice.

Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy

Cerebral amyloid angiopathy-related inflammation presenting with steroid-responsive higher brain dysfunction: case report and review of the literature

Cervical MRI of subacute myelo-optico-neuropathy

Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy).

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.

Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database.

Clinical trial network for the promotion of clinical research for rare diseases in Japan: muscular dystrophy clinical trial network

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

Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan

Cre/loxP-mediated adenovirus type 5 packaging signal excision demonstrates that core element VI is sufficient for virus packaging

DJ-1 forms complexes with mutant SOD1 and ameliorates its toxicity

Derlin-1 overexpression ameliorates mutant SOD1-induced endoplasmic reticulum stress by reducing mutant SOD1 accumulation

Detection and management of cardiomyopathy in female dystrophinopathy carriers

Diffusion and ADC-map images detect ongoing demyelination on subcortical white matter in an adult metachromatic leukodystrophy patient with autoimmune Hashimoto thyroiditis

Donor origin of multipotent adult progenitor cells in radiation chimeras

Dystrophin delivery to muscles of mdx mice using lentiviral vectors leads to myogenic progenitor targeting and stable gene expression.

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

Efficient and reproducible myogenic differentiation from human iPS cells: prospects for modeling Miyoshi Myopathy in vitro

Efficient repetitive gene delivery to skeletal muscle using recombinant adenovirus vector containing the Coxsackievirus and adenovirus receptor cDNA.

Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis.

Female dystrophinopathy: Review of current literature

Flexor-dominant myopathic phenotype in patients with His46Arg substitution in the Cu/Zn superoxide dismutase gene

Full-length dystrophin cDNA transfer into skeletal muscle of adultmdx mice by electroporation

Fulminant myelopathy following neurogenic proximal weakness associated with human T-cell lymphotropic virus type I infection

Heatstroke in patients with Parkinson’s disease

Long-Term Outcome of Polymyositis Treated with High Single-Dose Alternate-Day Prednisolone Therapy

Mdx respiratory impairment following fibrosis of the diaphragm

Medical Attitudes Survey for Female Dystrophinopathy Carriers in Japan

Multicenter questionnaire survey for sporadic inclusion body myositis in Japan

Muscle biopsy findings predictive of malignancy in rare infiltrative dermatomyositis

Muscle fiber type-predominant promoter activity in lentiviral-mediated transgenic mouse

Muscle-dominant wild-type TDP-43 expression induces myopathological changes featuring tubular aggregates and TDP-43-positive inclusions

Myasthenic crisis patients who require intensive care unit management

National registry of patients with Fukuyama congenital muscular dystrophy in Japan

Nationwide patient registry for GNE myopathy in Japan

Optineurin is potentially associated with TDP-43 and involved in the pathogenesis of inclusion body myositis

Prednisolone improves walking in Japanese Duchenne muscular dystrophy patients

Regions downstream from the WW domain of dystrophin are important for binding to postsynaptic densities in the brain

Rescue from respiratory dysfunction by transduction of full-length dystrophin to diaphragm via the peritoneal cavity in utrophin/dystrophin double knockout mice

Respiratory and cardiac function in japanese patients with dysferlinopathy

Serum Osteopontin as a Novel Biomarker for Muscle Regeneration in Duchenne Muscular Dystrophy

Significant CMAP decrement by repetitive nerve stimulation is more frequent in median than ulnar nerves of patients with amyotrophic lateral sclerosis

Social involvement issues in patients with Becker muscular dystrophy: A questionnaire survey of subjects from a patient registry

Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophin

Study of Duchenne muscular dystrophy long-term survivors aged 40 years and older living in specialized institutions in Japan

Successful treatment with rituximab and thalidomide of POEMS syndrome associated with Waldenstrom macroglobulinemia.

Survey on genetic counseling and health management for symptomatic and asymptomatic female dystrophinopathy carriers in Japan today

The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations

The TREAT-NMD Duchenne muscular dystrophy registries: conception, design, and utilization by industry and academia

The association between dermatomyositis and papillary thyroid cancer: a case report

Tongue strength in patients with subacute myelo-optico-neuropathy.

Transduction of Full-length Dystrophin to Multiple Skeletal Muscles Improves Motor Performance and Life Span in Utrophin/Dystrophin Double Knockout Mice

Treatment of a Japanese Patient with Familial Amyloidotic Polyneuropathy with Orthotopic Liver Transplantation

Trends in steroid therapy for Duchenne muscular dystrophy in Japan

Tumefactive multiple sclerosis

Usefulness of intraventricular infusion of antifungal drugs through Ommaya reservoirs for cryptococcal meningitis treatment.