スポンサーリンク
Department of Neurology, Juntendo University School of Medicine | 論文
- Peripheral Arterial Atherosclerosis in Patients with Extracranial, not Intracranial, Arterial Stenosis
- Mutational Analysis of Fukutin Gene in Dilated Cardiomyopathy and Hypertrophic Cardiomyopathy(Molecular Cardiology)
- Linear Medullary Pericanal Lesion with Longitudinal Myelitis can be Diagnostic of Neuromyelitis Optica
- Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium
- Glial localization of four-repeat tau in atypical progressive supranuclear palsy
- LRRK2 P755L variant in sporadic Parkinson's disease
- Autosomal recessive juvenile parkinsonism : A key to understanding nigral degeneration in sporadic Parkinson's disease
- Expression of functional Toll-like receptor 2 on human epidermal keratinocytes
- Homogeneous epithelial γδ T cell repertoire of the skin is shaped through peripheral selection
- Rationale and Design of the Carotid Plaque in Human for All Evaluations With Aggressive Rosuvastatin Therapy (CHALLENGER Trial) : Evaluation by Magnetic Resonance Imaging(Imaging)
- Neurotrophic and neuroprotective effects of neuron-specific enolase on cultured neurons from embryonic rat brain
- Blurred Vision With Acute Hypertension Indicating Hypertensive Brainstem Encephalopathy : Case Report
- Therapeutic Efficacy of Interferon β-1b in Japanese Patients with Optic-Spinal Multiple Sclerosis
- Apoptosis in Neurodegenerative Disorders
- Autosomal recessive early -onset parkinsonism with diurnal fluctuation : clinicopathologic characteristics and molecular genetic identification
- Pathological and biochemical studies on a case of Pick disease with severe white matter atrophy
- Posterior Reversible Encephalopathy Syndrome Complicating Intracranial Hemorrhage After Phenylpropanolamine Exposure : Case Report
- Genotype-phenotype correlation : Familial Parkinson disease
- PLA2G6 variant in Parkinson's disease
- Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease