Tanaka Toshiaki | Division Of Endocrinology And Metabolism National Research Center For Child Health And Development

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概要

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著作論文

ターナー症候群の新しい参照成長曲線(パーセンタイル曲線)の作成
Case Study of a 15-Year-old Boy with McCune-Albright Syndrome Combined with Pituitary Gigantism : Effect of Octreotide-long Acting Release (LAR) and Cabergoline Therapy
Four Japanese Patients with Adrenal Hypoplasia Congenita and Hypogonadotropic Hypogonadism Caused by DAX-1 Gene Mutations : Mutant DAX-1 Failed to Repress Steroidogenic Acute Regulatory Protein (StAR) and Luteinizing Hormone β-subunit Gene Promoter Activi
A Novel Mutation of the Steroidogenic Acute Regulatory Protein (StAR) Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
Novel SLC12A1 (NKCC2) Mutations in Two Families with Bartter Syndrome Type 1
A Novel Missense Mutation (P366T) of the LHX4 Gene Causes Severe Combined Pituitary Hormone Deficiency with Pituitary Hypoplasia, Ectopic Posterior Lobe and a Poorly Developed Sella Turcica
A Japanese Patient of Congenital Hypothyroidism with Cerebellar Atrophy
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
Serum Concentrations of BNP and ANP in Patients with Thyrotoxicosis
Standardization of Blood Growth Hormone Levels Measured by Different Kits Using a Linear Structural Relationship
Trends in Age and Anthropometric Data at Start of Growth Hormone Treatment for Girls with Turner Syndrome in Japan
Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome
Prediction of Pubertal Growth at Start of Estrogen Replacement Therapy in Turner Syndrome
Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan
Low-dose Growth Hormone Treatment (0.175mg/kg/week) for Short Stature in Patients with Turner Syndrome : Data from KIGS Japan
Replacement of Alanine with Asparagic Acid at Position 203 in Human Steroidogenic Acute Regulatory Protein Impairs the Ability to Enhance Steroidogenesis in vitro
Clinical Characteristics, Etiologies and Pathophysiology of Patients with Severe Short Stature with Severe GH Deficiency : Questionnaire Study on the Data Registered with the Foundation for Growth Science, Japan
Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
Statural Growth in 31 Japanese Patients with SHOX Haploinsufficiency : Support for a Disadvantageous Effect of Gonadal Estrogens
A Novel Heterozygous Mutation of Steroidogenic Factor-1 (SF-1/Ad4BP) Gene (NR5A1) in a 46, XY Disorders of Sex Development (DSD) Patient without Adrenal Failure
Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism
Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome
Clinical characteristics of Japanese adults with growth hormone deficiency : a HypoCCS database study

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