Eating Disorders in Patients with Juvenile-Onset Type 1 Diabetes Mellitus
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概要
- 論文の詳細を見る
- 2000-12-01
著者
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Urakami Tatsuhiko
Department of Pediatries, Nihon University School of Medicine
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OWADA MISAO
Department of Pediatrics, Nihon University School of Medicine
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Urakami Tatsuhiko
Department Of Pediatrics Nihon University School Of Medicine
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Owada Misao
Department Of Pediatrics Nihon University Hospital
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FUJII Shinichirou
Department of Pediatrics, Nihon University School of Medicine
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KUBO Mitsumasa
Department of Pediatrics, Nihon University School of Medicine
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Kubo Mitsumasa
Department Of Pediatrics Nihon University School Of Medicine
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Urakami Tatsuhiko
Department Of Pediatrics Advanced Medical Research Center Nihon University School Of Medicine
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Fujii Shinichirou
Department Of Pediatrics Nihon University School Of Medicine
関連論文
- Recent Change in the Annual Incidence of Childhood Type 2 Diabetes in the Tokyo Metropolitan Area
- 小児期発症1型糖尿病におけるインスリン、メトホルミン併用療法の有用性について
- A Case of Acute Lymphoblastic Leukemia with Prader-Willi Syndrome during Growth Hormone Therapy
- Characteristics of a Fulminant Onset Form of Idiopathic Type 1 Diabetes Mellitus in Japanese Children
- Frequencies of factors of metabolic syndrome at diagnosis in children with T2DM
- Acute lymphoblastic leukemia in a patient with Prader-Willi syndrome under growth hormone therapy
- Growth Hormone Effects in Two Children with Prader-Willi Syndrome
- Changes in Glycemic Control and Quality of Life in Pediatric Type 1 Diabetics with Continuous Subcutaneous Insulin Infusion of Insulin Aspart Following Multiple Daily Injection Therapy
- Treatment for Childhood Type 2 Diabetes
- Effect of growth hormone therapy in two sisters with SHOX haploinsufficiency
- Eating Disorders in Patients with Juvenile-Onset Type 1 Diabetes Mellitus
- A novel missense mutation in the thyroid hormone receptor β gene in a kindred with resistance to thyroid hormone
- A Case of Deoxycorticosterone-Producing Adrenal Adenoma
- Early onset distal muscular dystrophy with normal dysferlin expression
- Prenatal Diagnosis Reveals the Relative Frequencies of Lysosomal Storage Diseases in Japan
- Novel missense mutation in the purine nucleoside phosphorylase gene in a Japanese patient with purine nucleoside phosphorylase deficiency
- A newly identified exonic mutation of the WT1 gene in a patient with Denys-Drash syndrome
- Usefulness of HbA1c to diagnose diabetes among Japanese children detected by a urine glucose screening program in the Tokyo Metropolitan Area
- Comparison of the injection frequencies employed and basal-to-total insulin dose ratios obtained when glargine and detemir are used in children with type 1 diabetes mellitus treated by basal-bolus therapy
- Utility of an Increment in the Basal Rate during Mealtime in Place of Pre-meal Boluses for Preschool-aged Children with Type 1 Diabetes Using CSII
- Association between Sex, Age, Insulin Regimens and Glycemic Control in Children and Adolescents with Type 1 Diabetes
- Pathogenic Characteristics at Diagnosis in Young Children with Type 1 Diabetes Presenting Prior to 5 Years of Age