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Department of Internal Medicine, Aichi Medical University School of Medicine | 論文
- Deficiency of forkhead box P3 and cytotoxic T-lymphocyte-associated antigen-4 gene expressions and impaired suppressor function of CD4+CD25+ T cells in patients with autoimmune hepatitis
- Clinicopathologic characteristics of five autopsied cases of dura mater-associated Creutzfeldt-Jakob disease
- Investigation of visual disorders of subacute myelo-optico-neuropathy (SMON) patients 32 years after onset : Questionnaire-based survey and ophthalmological examination
- Zep: A Novel Zinc Finger Protein Containing a Large Proline-Rich Domain
- Familial Amyotrophic Lateral Sclerosis with a Novel G85S Mutation of Superoxide Dismutase 1 Gene: Clinical Features of Lower Motor Neuron Disease
- Enhanced Aquaporin-4 immunoreactivity in sporadic Creutzfeldt-Jakob disease
- Underediting of GluR2 mRNA, a neuronal death inducing molecular change in sporadic ALS, does not occur in motor neurons in ALS1 or SBMA
- Autopsy case of sporadic Creutzfeldt-Jakob disease presenting with signs suggestive of brainstem and spinal cord involvement
- Obstructive Sleep Apnea Syndrome (OSAS) Presenting as Cerebral Venous Thrombosis
- Multiple Cerebellar Infarcts : Clinical and Pathophysiologic Features
- Rapidly Progressive Fatal Respiratory Failure (Ondine's Curse) in the Lateral Medullary Syndrome
- Inflammatory pathological changes in a 2-year-old boy with Charcot-Marie-Tooth disease
- The Protective Effect of a Parsistent Trigeminal Artery on Brain Stem Infarctions: A Follow-up Case Report
- Widespread spinal cord involvement in progressive supranuclear palsy
- Paradoxical Brain Embolism Induced by Mycoplasma pneumoniae Infection with Deep Venous Thrombus
- X-linked Recessive Bulbospinal Neuronopathy (SBMA)
- Clinical and Pathophysiological Features of Amaurosis Fugax in Japanese Stroke Patients
- Crow-Fukase syndrome
- Pain-related Differential Expression of NGF, GDNF, IL-6, and Their Receptors in Human Vasculitic Neuropathies
- Pyramidal tract degeneration in sporadic Creutzfeldt-Jakob disease