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
スポンサーリンク
概要
- 論文の詳細を見る
- 2009-10-01
著者
-
Tanaka T
The Foundation For Growth Science
-
磯島 豪
Clinical Research Center National Center For Child Health And Development
-
YOKOYA Susumu
Clinical Research Center, National Center for Child Health and Development
-
ITO Junko
The Foundation for Growth Science
-
HORIKAWA Reiko
Clinical Research Center, National Center for Child Health and Development
-
TANAKA Toshiaki
The Foundation for Growth Science
-
Horikawa R
Division Of Endocrinology And Metabolism National Center For Child Health And Development
-
Horikawa Reiko
国立成育医療センター研究所 小児思春期発育研究部
-
Horikawa Reiko
Clinical Research Center National Center For Child Health And Development
-
Yokoya S
Clinical Research Center National Center For Child Health And Development
-
Yokoya Susumu
国立成育医療センター 臨床検査部
-
Tajima T
Department Of Pediatrics Hokkaido University School Of Medicine
-
Takezaki Toshiro
北海道大学 小児科学
-
Yokoya Susumu
Clinical Pediatric Endocrinology
-
Tsushima T
Tokyo Women's Medical Univ. Tokyo Jpn
-
Tsushima Toshio
Department Of Endocrinology Clinical Institute Of Endocrinology Tokyo Women's Medical Universit
-
Tanaka Toshiaki
Department Of Pediatrics Hokkaido University School Of Medicine
-
Takezaki Toshiro
Department Of Pediatrics Hokkaido University School Of Medicine
-
Tajima Toshihiro
国立成育医療センター 臨床検査部
-
Isojima Tsuyoshi
Clinical Research Center National Center For Child Health And Development
-
Tanaka T
Department Of Obstetrics And Gynecology Faculty Of Medicine University Of Tokyo
-
Tanaka Toshiaki
Division Of Endocrinology And Metabolism National Research Center For Child Health And Development
-
Tanaka Toshiaki
Department Of Endocrinology And Metabolism National Children's Hospital
関連論文
- Expression of Messenger RNA of Insulin-Like Growth Factors(IGFs)and IGF Binding Proteins(IGFBP1-6)in Placenta of Normal and Diabetic pregnancy
- Serum Levels of Free Insulin-Like Growth Factor (IGF)-I in Normal Children
- 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
- Two Novel Aquaporin-2 Mutations in a Sporadic Japanese Patient with Autosomal Recessive Nephrogenic Diabetes Insipidus
- A Case of Achondroplasia Associated with Cervicomedullary-Junction Compression
- Two Novel Mutations of Thiazide-Sensitive Na-Cl Cotransporter (TSC) Gene in Two Sporadic Japanese Patients with Gitelman Syndrome
- Turner Syndrome with Crohn Disease
- Two mutations of the Gsα gene in two Japanese patients with sporadic pseudohypoparathyroidism type Ia
- Evaluation of Bone Mineral Density in Patients with Turner Syndrome
- A novel missense mutation in the HMG box region of the SRY gene in a Japanese patient with an XY sex reversal
- A Japanese Case with Frasier Syndrome Caused by the Splice Junction Mutation of WT1 Gene
- Mutations of the CYP21 Gene in Nonclassical Steroid 21-Hydroxylase Deficiency in Japan
- Prenatal Diagnosis of Steroid 21-Hydroxylase Deficiency by the Modified Polymerase Chain Reaction to Detect Splice Site Mutation in the CYP21 Gene
- PREDOMINANCE OF THE MUTATION AT 1138 OF THE cDNA FOR THE FIBROBLAST GROWTH FACTOR RECEPTOR 3 IN JAPANESE PATIENTS WITH ACHONDROPLASIA
- A Japanese Patient of Congenital Hypothyroidism with Cerebellar Atrophy
- 64 ADRENO-GENITO-RENAL DISORDER WITH SEVERE GROWTH FAILURE : A NEW DISEASE
- 82 MATERNAL UNIPARENTAL ISODISOMY FOR CHROMOSOME 7 IN A CASE WITH SILVER-RUSSELL SYNDROME
- 132 A CASE OF VIRILIZING ADRENOCORTICAL TUMOR
- 152 Dose an anabolic steroid rescue final heights of gonadal suppression therapy?
- 19 GROWTH HORMONE-RELEASING HORMONE (GHRH) RECEPTOR MUTATION THAT ACTS AS A DOMINANT NEGATIVE.
- 52 STUDIES OF HEPATOCYTE NUCLER FACTER-4α HNF4-α AND HNF-1β GENES IN JUVENILE ONSET DIABETES MELLITUS WITHOUT OBESITY
- 125 EFFECT OF ANABOLIC STEROID HORMONE ON GROWTH PROMOTION AND GONADAL FUNCTION IN PUBERTAL BOYS
- 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
- Metabolic Effects of Human Growth Hormone Isoform (20k-hGH) in Adults with Growth Hormone Deficiency
- Metabolic Effects of Human Growth Hormone Isoform (20 k-hGH) in Adults with Growth Hormone Deficiency
- Serum Concentrations of BNP and ANP in Patients with Thyrotoxicosis
- Leptin Regulation of the Thyroids : Negative Regulation on Thyroid Hormone Levels in Euthyroid Subjects and Inhibitory Effects on Iodide Uptake and Na^+/I^- Symporter mRNA Expression in Rat FRTL-5 Cells
- Increased Expression of Phosphorylated p70S6 Kinase and Akt in Papillary Thyroid Cancer Tissues
- Serum Leptin Levels and Bioelectrical lmpedance Assessment of Body Composition in Patients with Graves' Disease and Hypothyroidism
- Effect of Cytokines on Producton of Insulin-like Growth Factor Binding Proteins (IGFBPs) from Human Fibroblasts in Culture
- Interaction between Leptin and Growth Hormone (GH)/IGF-I Axis
- Expression of Insulin-Like Growth Factor Binding Proteins(IGDBPs)in Human Thyroid Papillary Cancer Tissues
- Expression of Recombinant Human Thyrotropin Receptor in Myeloma Cells
- Pharmacokinetics and Metabolic Effects of High-Dose Growth Hormone Administration in Healthy Adult Men
- Carboxy-Terminal Propeptide of Type 1 Procollagen (P1CP)and Carboxy-Terminal Telopeptide of Type 1 Collagen (1CTP) as Sensitive Markers of Bone Metabolism in Thyroid Disease
- 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
- INSULIN-LIKE GROWTH FACTOR I AFFECTING CARDIAC HYPERTROPHY IN HUMAN DISEASED MYOCARDIUM : Cardiomyopathy, Myocarditis : 53 Annual Scientific Meeting, Japanese Circulation Society
- Mortality in Patients with Congenital 21-Hydroxylase Deficiency Diagnosed after the Introduction of a Newborn Screening Program in Japan
- Standardization of Blood Growth Hormone Levels Measured by Different Kits Using a Linear Structural Relationship
- Final Height of Growth Hormone (GH)-Treated Short Children Registered at the Foundation for Growth Science in Japan : Comparison between the Pituitary Human GH Era and the Recombinant Human GH Era
- Postoperative Plasma Cortisol Levels Predict Long-Term Outcome in Patients with Cushing's Disease and Determine Which Patients Should be Treated with Pituitary Irradiation after Surgery
- Registration System for Growth Hormone (GH) Treatment with Standardized Immunoreactive GH Values in Japan
- Growth factors that modulate growth and functions of thyroid cells in culture
- 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
- No Improvement of Adult Height in Non-growth Hormone (GH) Deficient Short Children with GH Treatment
- Studies of Very Severe Short Stature with Severe GH Deficiency : From the Data Registered with the Foundation for Growth Science
- Serum Levels of 20-Kilodalton Human Growth Hormone (GH) in Children with Simple Obesity
- The Comparison of the Effects of Short-Term Growth Hormone Treatment in Patients with Achondroplasia and with Hypochondroplasia
- Serum Levels of Free Insulin-Like Growth Factor (IGF)-I in Normal Children ; Relations to Total IGF-I, IGF Binding Protein (IGFBP)-1, IGFBP-3, and Acid Labile Subunit (ALS)
- Complications in Adults with Growth Hormone Deficiency : A Survey Study in Japan
- Insulin-Like Growth Factors (IGFs) and IGF-Binding Proteins (IGFBP-1, -2 and -3) in Diabetic Pregnancy:Relationship to Macrosomia
- Elevated Serum Bisphenol A Levels under Hyperandrogenic Conditions may be Caused by Decreased UDP-glucuronosyltransferase Activity
- Differences in Serum Bisphenol A Concentrations in Premenopausal Normal Women and Women with Endometrial Hyperplasia
- A Case of Female Pseudohermaphroditism Caused by Aromatase Deficiency
- Viriizing Adrenocortical Carcinoma Invading the Right Atrium with Histological High-Grade Malignancy and p53 Mutation in a 3-Year-Old Child : Indication of Post Operative Adjuvant Chemotherapy
- The Usefulness of GnRH and hCG Testing for the DifferentiaI Diagnosis of Delayed Puberty and Hypogonadotropic Hypogonadism in Prepubertal Boys
- Disorders of the Hypothalamic-Pituitary-Adrenal Axis Caused by Overdosed Anti-Allergic Drug : A Case Report
- A Ten-Year Old Male with Bromocriptine Resistant PRL and GH-Producing Huge Pituitary Adenoma
- 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
- Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
- Two Novel Mutations in the Thyroid Peroxidase Gene with Goitrous Hypothyroidism
- Statural Growth in 31 Japanese Patients with SHOX Haploinsufficiency : Support for a Disadvantageous Effect of Gonadal Estrogens
- Height Responses in Complete ldiopathic Growth Hormone Deficient Children Less Than Three Years of Age during Growth Hormone Therapy
- 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
- Growth-Promoting and Psychological Effects of High-Dose Growth Hormone Treatment in Children with Intrauterine Growth Retardation
- Follow-Up Study of Children with Precocious Puberty Treated with Cyproterone Acetate
- Spontaneous Growth in Hormone-Treated Short Children
- Growth Response to Growth Hormone Therapy in Patients with Different Degrees of Growth Hormone Deficiency
- 太陽フレアーにおける融合不安定
- Clinical Outcome of GH Treatment in Turner Girls in Japan : Results of Multicentre Trial
- Platelet Epidermal Growth Factor in Thyroid Disorders
- Timing for Discontinuation of Treatment with a Long-Acting Gonadotropin-Releasing Hormone Analog in Girls with Central Precocious Puberty
- Comparative Concentrations of Growth Hormone-Binding Protein in Maternal Circulation, Fetal Circulation, and Amniotic Fluid
- Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
- Preface
- Nutrition Related Hormonal Changes in Obese Children
- Combined GH and LHRH Analog Treatment in Short Children
- Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism
- 39 SIBLING CASES OF HEREDITARY HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA
- 112 METABOLIC SYNDROME IN SURVIVORS OF CHILDHOOD BRAIN TUMORS WITH ENDOCRINE COMPLICATIONS
- 18 Sporadic haploinsufficiency of the HESX1 gene causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient
- 117 Molecular analysis of PHEX and FGF23 gene in hypophosphatemic rickets
- 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