HASEGAWA TOMONOBU | Department of Pediatrics, Keio University School of Medicine

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概要

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著作論文

Mutation of a Gene for Thyroid Transcription Factor-1 (TITF1) in a Patient with Clinical Features of Resistance to Thyrotropin
Four novel mutations of the Fanconi anemia group A gene (FAA) in Japanese patients
Analysis of the NSD1 promoter region in patients with a Sotos syndrome phenotype
Final Height of Female Patients with Early-onset Anorexia Nervosa
Final Height of Female Patients with Early-onset Anorexia Nervosa
Lack of Correlation between the Endocrinological Abnormalities and Obesity Index in Anorexia Nervosa in Childhood and Adolescence
A Case of a Preterm Infant with 21-Hydroxylase Deficiency : Implications of the Biochemical Diagnosis with Urinary Pregnanetriolone by Gas Chromatography/Mass Spectrometry in Selected Ion Monitoring (GCMS-SIM)
A Case of Pediatric Virilizing Adrenocortical Tumor Resulting in Hypothalamic-pituitary Activation and Central Precocious Puberty Following Surgical Removal
The Circadian Variation of Cortisol Secretion in Patients with Anorexia Nervosa in Childhood and Adolescence after Recovery of Body Weight by Treatment Using Gas Chromatography/Mass Spectrometry in Selected Ion Monitoring
Reference Values for Urinary Steroids in Japanese Newborn Infants : Gas Chromatography/Mass Spectrometry in Selected Ion Monitoring
Association of Micropenis with Pro185Ala Polymorphism of the Gene for Aryl Hydrocarbon Receptor Repressor Involved in Dioxin Signaling
Clinical Utility of Insulin-Like Growth Factor-l(IGF-I)and IGF Binding Protein-3 Levels in the Diagnosis of GH Deficiency(GHD)During Childhood
Mutational Analysis of Androgen Receptor (AR) Gene in 46, XY Patients with Ambiguous Genitalia and Normal Testosterone Secretion : Endocrinological Characteristics of Three Patients with AR Gene Mutations
Development of Growth Hormone and Adrenocorticotropic Hormone Deficiencies in Patients with Prenatal or Perinatal-Onset Hypothalamic Hypopituitarism Having Invisible or Thin Pituitary Stalk on Magnetic Resonance Imaging
Joint laxity, vitreoretinal degeneration, facial abnormalities, and generalized skeletal alterations : A new syndrome?
Clinical findings and P450 Oxidoreductase (POR) gene analysis in Antley-Bixler syndrome with abnormal genitalia
Growth Failure in an Infant with Congenital Nephrogenic Diabetes Insipidus During Sodium Restriction
A Novel Mutation of Androgen Receptor Gene in Complete Androgen Insensitivity Syndrome
Mental Retardation in a Boy with Congenital Adrenal Hypoplasia : A Clue to Contiguous Gene Syndrome Involving DAX1 and IL1RAPL

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