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Departments Of Neurology Hematology Metabolism Endocrinology And Diabetology Faculty Of Medicine Yam | 論文
- Low concentration of serum haptoglobin has impact on understanding complex pathophysiology in patients with acquired bone marrow failure syndromes
- Genetic Association between Aldehyde Dehydrogenase 2 (ALDH2) Variation and High-Density Lipoprotein Cholesterol (HDL-C) Among Non-Drinkers in Two Large Population Samples in Japan
- Association of an intronic haplotype of the LIPC gene with hyperalphalipoproteinemia in two independent populations
- An Unusual Case of Hypertensive Encephalopathy Involving the Brain Stem
- Type 2 Diabetes is Not a Risk Factor for Asymptomatic Ischemic Brain Lesion-The Funagata Study
- Pioglitazone (AD-4833) Ameliorates Insulin Resistance in Patients with NIDDM
- Pontine and extrapontine myelinolysis in a patient with acute lymphocytic leukemia who had hypernatremia before the onset of neurological symptomes
- Osmoregulation of Vasopressin Secretion in Patients with the Syndrome of Inappropriate Antidiuresis Associated with Central Nervous System Disorders
- Thiazolidinediones Exert Different Effects on Insulin Resistance between Dexamethasone-Theated Rats and Wistar Fatty Rats
- Sequential Changes in CGRP-like Immunoreactivity in NIDDM Model Otsuka Long-Evans Tokushima Fatty (OLETF) Rat Pancreatic Islets
- Slight but Significant Improvement of Insulin Resistance of Wistar Fatty Rats by Treatment with a Disaccharidase Inhibitor, AO-128
- Hyper-Adrenocorticotropinemia in a Patient with Addison's Disease after Treatment with Corticosteroids
- A POINT MUTATION, C TO T, IN EXON 8 OF THE PORPHOBILINOGEN DEAMINASE GENE IN A JAPANESE FAMILY WITH ACUTE INTERMITTENT PORPHYRIA
- Insulin-Like Growth Factor I Resistance in Peripheral Tissue but not in Liver in Streptozotocin-Induced Diabetic Rats
- A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family
- A novel autoantibody in paraneoplastic sensory-dominant neuropathy
- Binding of IDPN (β, β' -iminodipropionitrile) to rat spinal cord: Possible implication in the mechanism of spheroid formation in amyotrophic lateral sclerosis)
- Hereditary ceruloplasmin deficiency: A cerebro-retino-diabetic disease
- Ultrastructural localization of heparan sulfate-like immunoreactivity in spinal spheroids of motor neuron disease
- Hereditary Ceruloplasmin Deficiency - A New Type of Diabetes Mellitus