インスリン微量変動法の血糖コントロールに対する有効性の検討
スポンサーリンク
概要
- 論文の詳細を見る
- 2004-12-01
著者
-
HARA Toshiro
Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University
-
都 研一
Department Of Endocrinology And Metabolism Fukuoka Children's Hospital
-
KUROMARU RYUICHI
Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University
-
KOHNO HITOSHI
Department of Endocrinology and Metabolism, Fukuoka Children's Hospital
-
Hara Toshiro
Department Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine
-
Kohno H
Department Of Endocrinology And Metabolism Fukuoka Children's Hospital
-
Miyako Kenichi
Department Of Endocrinology And Metabolism Fukuoka Children's Hospital
-
Kohno Hitoshi
Department Of Endocrinology And Metabolism Fukuoka Children's Hospital
-
Kuromaru Ryuichi
Department Of Pediatrics Graduate School Of Medical Sciences Kyushu University
関連論文
- A novel R275X mutation of the SLC25A15 gene in a Japanese patient with the HHH syndrome
- Early-Onset Thyrotoxicosis after Unrelated Cord Blood Transplantation for Acute Myelogenous Leukemia
- Unrelated Cord Blood Transplantation with a Reduced-Intensity Conditioning Regimen following Autologous Transplantation for Multiple Myeloma
- Association of IL12RB1 Polymorphisms with Susceptibility to and Severity of Tuberculosis in Japanese : a Gene-based Association Analysis of 21 Candidate Genes
- Long-Term Outcome of Treatment With Protocols AL841, AL851, and ALHR88 in Children With Acute Lymphoblastic Leukemia: Results Obtained by the Kyushu-Yamaguchi Children's Cancer Study Group
- 出生体重と3歳児体容量指数(body mass index)の関連
- インスリン微量変動法の血糖コントロールに対する有効性の検討
- 遅発型オルニチントランスカルバミラーゼ欠損症男性患者における予後因子と血漿アミノ酸プロフィールの特徴
- Growth Hormone (GH) Effects on Central Fat Accumulation in Adult Japanese GH Deficient Patients : 6-month Fixed-dose Effects Persist during Second 6-month Individualized-dose Phase
- Successful Unrelated Cord Blood Transplantation for Epstein-Barr Virus-Associated Lymphoproliferative Disease with Hemophagocytic Syndrome
- Dominant β-Thalassemia with Hemoglobin Hradec Kralove : Enhanced Hemolysis in the Spleen
- Quantitative Monitoring of Circulating Epstein-Barr Virus DNA for Predicting the Development of Posttransplantation Lymphoproliferative Disease
- Neuron-Specific Enolase in Hemophagocytic Lymphohistiocytosis: A Potential Indicator for Macrophage Activation?
- Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people
- Low-Dose Granulocyte Colony-Stimulating Factor Overcomes Neutropenia in the Treatment of Non-Hodgkin's Lymphoma with Higher Cost-Effectiveness
- A Ten-Year Old Male with Bromocriptine Resistant PRL and GH-Producing Huge Pituitary Adenoma
- Plasma Cell Leukemia with Myelofibrosis
- A Variant Form of Acute Promyelocytic Leukemia with Marked Myelofibrosis
- 重症先天性横隔膜ヘルニアにおける RS (respiratory syncytial) ウイルス感染の危険性
- Attenuation of cardiotoxicity of daunomycin using a complex with heparin
- Inducible and endothelial constitutive nitric oxide synthase gene polymorphisms in Kawasaki disease
- Novel polymorphism in the 5'-untranslated region of the interleukin-4 gene
- A Case of Growth Hormone and Gonadotropin Deficiency Associated with Unilateral Anophthalmia, Microphallus, Cryptorchidism, and Mental Retardation
- Long-Term Effect of Growth hormone (GH) Treatment on Body Composition in Children with GH Deficiency
- The relationship between retrieval success and task performance during the recognition of meaningless shapes : An event-related near-infrared spectroscopy study
- Delayed Onset of Systemic Bacterial Dissemination and Subsequent Death in Mice Injected Intramuscularly with Streptococcus pyogenes Strains
- Magnetic resonance studies of brain lesions in patients with Kawasaki disease
- Diagnostic usefulness of diffusion-weighted magnetic resonance imaging in influenza-associated acute encephalopathy or encephalitis
- Abolishment of Pleural Effusion as the Initial Manifestation of Chronic Myelomonocytic Leukemia without Chemotherapy
- Expression of survivin and of antigen detected by a novel monoclonal antibody, T332, is associated with outcome of diffuse large B-cell lymphoma and its subtypes
- Acute Myeloid Leukemia With t(11;19) (q23;pl3) Developing in an Adult T-Cell Leukemia Patient Treated With Combined Chemotherapy Including Etoposide
- Renal Tubular Acidosis Associated With Zonisamide Therapy
- Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in Japan
- Genetic susceptibility to febrile seizures : Case-control association studies
- Lymphoid Blast Crisis During Interferon-α Therapy in a Patient With Chronic Myelogenous Leukemia in Myeloid Blast Crisis
- Hydroxyurea-Induced Fever in a Patient With Chronic Myelogenous Leukemia
- Vitamin D deficiency rickets caused by improper lifestyle in Japanese children
- Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene
- Curative Surgery Improves the Survival of Patients with Perforating Colorectal Cancer
- Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan
- Cell Cycle-Dependent Priming Action of Granulocyte Colony-Stimulating Factor (G-CSF) Enhances in vitro Apoptosis Induction by Cytarabine and Etoposide in Leukemia Cell Lines
- Improvement in the outcome of patients with antenatally diagnosed congenital diaphragmatic hernia using gentle ventilation and circulatory stabilization
- 145 PROSECTIVE STUDY OF BODY COMPOSITION AND LIPID PROFILES DURING GROWTH HORMONE TREATMENT IN CHILDREN WITE TURNER SYNDROME
- 37 2 CACES OF ALLGROVE SYNDROME WITH A MUTATION IN THE AAAS GENE
- Coexistence of inversion 16 and the Philadelphia chromosome comprising P190 BCR/ABL in chronic myeloid leukemia blast crisis
- Vitamin D deficiency presenting in an infant with neonatal lupus erythematosus
- 50 ASSOCIATION STUDY OF HUMAN MUT T HOMOLOGUE 1 GENE VAL83MET POLYMORPHISM WITH TYPE 1 DIABETES MELLrrus.
- Implications of surgical intervention in the treatment of neuroblastomas : 20-year experience of a single institution
- First report of drug-induced esophagitis by deferasirox
- Treatment of idiopathic pituitary dwarfism with methionyl human growth hormone.
- Association Study of Human MTH1 Gene Polymorphisms with Type 1 Diabetes Mellitus
- Guidance on the use of canakinumab in patients with cryopyrin-associated periodic syndrome in Japan
- Favorable Impact of Growth Hormone Treatment on Cholesterol Levels in Turner Syndrome