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The First Department Of Internal Medicine Kagawa Medical University | 論文
- Positioning Accuracy of Linac Radiosurgery
- A case of lung cancer associated with pneumoconiosis diagnosed by fluorine-18 fluorodeoxyglucose positron emission tomography
- Uptake of Fluorine-18-Fluorodeoxyglucose in Pulmonary Mycobacterium avium Complex Infection
- Clinical Features of Three Fatal Cases of Non-specific Interstitial Pneumonia
- Tc-99m Technegas scintigraphy to evaluate the lung ventilation in patients with oral corticosteroid-dependent bronchial asthma
- Thymic Carcinoma Associated with a High Serum Level of Interleukin 6 Diagnosed through the Evaluation for Asymptomatic Elevation of Acute-Phase Reactants
- Detection of Pneumocystis carinii Sequences in Serum by Polymerase Chain Reaction: Clinical Application in Two Patients with P. carinii Pneumonia
- Hepatocyte Growth Factor and Digital Clubbing
- Serial Measurements of Plasma Hepatocyte Growth Factor in Patients with Pneumonia Fllowing Cancer Chemotherapy
- Successful Autotransplantation of an Adrenal Gland Using a New Method of Omental Wrapping: Report of a Case
- Lymph Node Metastasis from Breast Cancer Diagnosed by F-18 FDG Whole-body PET (Case report)
- Spontaneous Rupture of a Parathyroid Adenoma Presenting as a Massive Cervical Hemorrhage : Report of a Case
- Recovery of Parathyroid Function After Total Thyroidectomy
- Small Cell Lung Cancer Associated with Systemic Sclerosis
- Different Phenotypes of Multiple Endocrine Neoplasia Type 1 (MEN1) in Monozygotic Twins Found in a Japanese MEN1 Family with MEN1 Gene Mutation
- Evidence for a Potential Role for HDL as an Important Source of Cholesterol in Human Adrenocortical Tumors Via the CLA-1 pathway
- A Novel Germline Mutation of Multiple Endocrine Neoplasia Type 1 (MEN1) Gene in a Japanese MEN1 Patient and Her Daughter
- A Family of MEN1 with a Novel Germline Messense Mutation and Benign Polymorphisms
- Germline Mutation of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene in a Family with Primary Hyperparathyroidism
- Detection of a Novel Nonsense Mutation of the MEN1 Gene in a Familial Multiple Endocrine Neoplasia Type 1 Patient and its Screening in the Family Members