スポンサーリンク
Division of Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori University | 論文
- Increased levels of GM_2 ganglioside in fibroblasts from a patient with juvenile Niemann - Pick disease type C
- Extraosseous epidural IgD myeloma presenting with compression myelopathy
- Steroid-Responsive Limbic Encephalitis
- Molecular Pathological Studies of Familial Amyotrophic Lateral Sclerosis
- Formation of advanced glycation end-productmodified superoxide dismutase-1 (SOD1) is one of the mechanisms responsible for inclusions common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutation, and transgenic mice expressing human S
- A case of brain-biopsy proven progressive multifocal leukoencephalopathy:Pathological findings and analysis of JC virus regulatory region
- Spontaneous Haemophilus Influenzae Type B Meningoventriculitis with Intraventricular Debris
- Familial limb pain in childhood : Unusual manifestation of migraine?
- Odorant evoked magnetic fields in humans
- Muscle weakness in a Japanese family of Arg1239His mutation hypokalemic periodic paralysis
- Branched-Chain Amino Acid Therapy for Spinocerebellar Degeneration:A Pilot Clinical Crossover Trial
- Japanese familial amyotrophic lateral sclerosis family with a two-base deletion in the sutperoxide dismutase-1 gene
- Prolonged silent periods produced by magnetic cortical stimulation in patients with cerebellar ataxia
- Vertical ophthalmoplegia in a demented patient with striatopallidodentate calcification
- Effective anticonvulsant therapy in a patient with limb shaking : A case report
- Epidemiology of inflammatory neurological and inflammatory neuromuscular diseases in Tottori Prefecture, Japan
- A NOVEL DOUBLE HETERO MUTATION FOUND IN THE METHYLENETETRAHYDROFOLATE REDUCTASE GENE IN A JUVENILE TIA