about
Efficient and reproducible myogenic differentiation from human iPS cells: prospects for modeling Miyoshi Myopathy in vitroPantothenate kinase-associated neurodegeneration initially presenting as postural tremor alone in a Japanese family with homozygous N245S substitutions in the pantothenate kinase geneCerebral amyloid angiopathy-related inflammation presenting with steroid-responsive higher brain dysfunction: case report and review of the literature.Drastic therapy for listerial brain abscess involving combined hyperbaric oxygen therapy and antimicrobial agents.Diffusion and ADC-map images detect ongoing demyelination on subcortical white matter in an adult metachromatic leukodystrophy patient with autoimmune Hashimoto thyroiditis.An adult norovirus-related encephalitis/encephalopathy with mild clinical manifestation.Muscle fiber type-predominant promoter activity in lentiviral-mediated transgenic mouse.Rescue from respiratory dysfunction by transduction of full-length dystrophin to diaphragm via the peritoneal cavity in utrophin/dystrophin double knockout mice.New type of Sendai virus vector provides transgene-free iPS cells derived from chimpanzee bloodGenotype-phenotype relationship in hereditary amyotrophic lateral sclerosis.Lateral Asymmetry and Spatial Difference of Iron Deposition in the Substantia Nigra of Patients with Parkinson Disease Measured with Quantitative Susceptibility MappingMulticenter questionnaire survey for sporadic inclusion body myositis in Japan.Pathomechanisms of anti-cytosolic 5'-nucleotidase 1A autoantibodies in sporadic inclusion body myositis.Effect of thymectomy for thymic atrophy in myasthenia gravis: A retrospective study on 93 patients.Clinical significance of CYLD downregulation in breast cancer.Decision making of amyotrophic lateral sclerosis patients on noninvasive ventilation to receive tracheostomy positive pressure ventilation.Abnormal spinal MRI findings in human T-cell lymphotrophic virus type I-associated myelopathy.Fulminant myelopathy following neurogenic proximal weakness associated with human T-cell lymphotropic virus type I infection.Derlin-1 overexpression ameliorates mutant SOD1-induced endoplasmic reticulum stress by reducing mutant SOD1 accumulation.Regions downstream from the WW domain of dystrophin are important for binding to postsynaptic densities in the brain.Meningitis and Ventriculitis due to Nocardia araoensis Infection.Usefulness of intraventricular infusion of antifungal drugs through Ommaya reservoirs for cryptococcal meningitis treatment.Cre/loxP-mediated adenovirus type 5 packaging signal excision demonstrates that core element VI is sufficient for virus packaging.Adenovirus-mediated murine interferon-gamma receptor transfer enhances the efficacy of IFN-gamma in vivo.Osteopontin-integrin α(v)β(3) axis is crucial for 5-fluorouracil resistance in oral squamous cell carcinoma.Hemiatrophy of the Tongue with Contralateral Hemiparesis in a Patient with Multifocal Acquired Demyelinating Sensory and Motor Neuropathy.Muscle biopsy findings predictive of malignancy in rare infiltrative dermatomyositis.Bcl-2 expression by retrograde transport of adenoviral vectors with Cre-loxP recombination system in motor neurons of mutant SOD1 transgenic mice.Effect on motor neuron survival in mutant SOD1 (G93A) transgenic mice by Bcl-2 expression using retrograde axonal transport of adenoviral vectors.Myasthenic crisis patients who require intensive care unit management.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 repetitive gene delivery to skeletal muscle using recombinant adenovirus vector containing the Coxsackievirus and adenovirus receptor cDNA.Acute ophthalmoparesis accompanied with Influenza A infection.Amyotrophic lateral sclerosis in a patient with Kartagener syndrome.Cervical MRI of subacute myelo-optico-neuropathy.Tumefactive multiple sclerosis.Tongue strength in patients with subacute myelo-optico-neuropathy.Thomsen disease with ptosis and abnormal MR findings.Coexistence of Amyotrophic Lateral Sclerosis and Myasthenia Gravis.Utility of skinfold thickness measurement in non-ambulatory patients with Duchenne muscular dystrophy.
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Satoshi Yamashita
@ast
Satoshi Yamashita
@en
Satoshi Yamashita
@es
Satoshi Yamashita
@nl
Satoshi Yamashita
@sl
type
label
Satoshi Yamashita
@ast
Satoshi Yamashita
@en
Satoshi Yamashita
@es
Satoshi Yamashita
@nl
Satoshi Yamashita
@sl
prefLabel
Satoshi Yamashita
@ast
Satoshi Yamashita
@en
Satoshi Yamashita
@es
Satoshi Yamashita
@nl
Satoshi Yamashita
@sl
P106
P1153
57196247050
7403456165
P31
P496
0000-0001-9315-3492