Horikawa Reiko | Division Of Endocrinology And Metabolism National Children's Hospital

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概要

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著作論文

Identification and characterization of cryptic SHOX intragenic deletions in three Japanese patients with Leri-Weill dyschondrosteosis
Seven Cases of Diabetes Mellitus in Turner Syndrome
Lipohypertrophy in a Patient with Isolated Growth Hormone Deficiency Type IA (IGHD IA) Treated with IGF-I
Latent Adrenal Insufficiency in Two Patients with Childhood-Onset Pitutary Hormone Deficiency
Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome
Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan
Replacement of Alanine with Asparagic Acid at Position 203 in Human Steroidogenic Acute Regulatory Protein Impairs the Ability to Enhance Steroidogenesis in vitro
The Comparison of the Effects of Short-Term Growth Hormone Treatment in Patients with Achondroplasia and with Hypochondroplasia
A Case of Female Pseudohermaphroditism Caused by Aromatase Deficiency
Growth Hormone (GH) Binding Protein in Children with Intrauterine Growth Retardation Treated with High Dose GH
Japanese Familial Patients with Male-Limited Precocious Puberty
Genetic and Endocrinological Evaluations of Three 46, XX Patients with Congenital Lipoid Adrenal Hyperplasia Previously Reported as Having Presented Spontaneous Puberty
Final Height in Girls with Turner Syndrome after Growth Hormone Treatment ; Experience at National Children's Hospital
Growth Hormone-Releasing Hormone Receptor Deficiency

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