Nagasaki Keisuke | Division Of Pediatrics Department Of Homeostatic Regulation And Development Niigata University Gradu

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著作論文

Usefulness of GPT for Diagnosis of Metabolic Syndrome in Obese Japanese Children
Mutation of a Gene for Thyroid Transcription Factor-1 (TITF1) in a Patient with Clinical Features of Resistance to Thyrotropin
Lower Birth Weight Associated with Current Overweight Status Is Related with the Metabolic Syndrome in Obese Japanese Children
Different Skeletal Phenotypes in a Mother and Two Daughters with Short Stature Homeobox-Containing Haploinsufficiency
Longitudinal Growth of the Short Bones of the Hand in a Girl with Pseudohypoparathyroidism Type Ia
Two Cases of Pseudohypoparathyroidism Type Ia in Duozygotic Twins with Different Phenotypes
Usefulness of Serum Adiponectin Level as a Diagnostic Marker of Metabolic Syndrome in Obese Japanese Children
The Levels of Serum Low-Density Lipoprotein Cholesterol Using Direct Measurement in Healthy Japanese School Children
Obese Japanese children have low bone mineral density after puberty
A Young Case of Severe Diabetic Ketoacidosis Due to Excess Ingestion of Soft Drinks : Necessity of Active Intervention for Child Obesity
26 The relationship between waist circumference, abdominal wall thickness. serum adiponectin and insulin, and metabolic syndrome in obese boys
Elevation of Serum C-Reactive Protein Levels Is Associated with Obesity in Boys
A Case of Female Pseudohermaphroditism Caused by Aromatase Deficiency
Spontaneous Regression of Isolated Neurohypophyseal Langerhans Cell Histiocytosis with Diabetes Insipidus
Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome
Metabolic effects of growth hormone replacement in two pediatric patients with growth without growth hormone
Autonomously functioning thyroid nodule in a four-year-old boy with Sotos syndrome
The occurrence of neonatal acute respiratory disorders in 21-hydroxylase deficiency
Novel C617Y mutation in the 7th transmembrane segment of luteinizing hormone/choriogonadotropin receptor in a Japanese boy with peripheral precocious puberty
A novel homozygous mutation of the nicotinamide nucleotide transhydrogenase gene in a Japanese patient with familial glucocorticoid deficiency

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