Combined GH and LHRH Analog Treatment in Short Children

スポンサーリンク

概要

• 論文の詳細を見る
• 1996-10-01

著者

• Tanaka T

  The Foundation For Growth Science

• TANAKA TOSHIAKI

  Division of Endocrinology and Metabolism, National Center for Child Health and Development

• Satoh Mari

  Department of Pediatrics, Toho University

• HIBI Itsuro

  Division of Endocrinology & Metabolism, National Children's Hospital

• Hibi I

  Division Of Endocrinology & Metabolism National Children's Hospital

• Satoh M

  First Department Of Pediatrics Toho University School Of Medicine

• Satoh Mari

  Department Of Endocrinology And Metabolism National Children's Medical Research Center

• Tanaka Toshiaki

  Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm

• Tanaka Toshiaki

  Division Of Endocrinology And Metabolism National Center For Child Health And Development

関連論文

• 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
• 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
• 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
• Determination of specific activities and kinetic constants of biotinidase and lipoamidase in LEW rat and Lactobacillus casei (Shirota)
• 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
• Pharmacokinetics and Metabolic Effects of High-Dose Growth Hormone Administration in Healthy Adult Men
• Autoimmune Thyroid Disease in Children and Adolescents With Idiopathic Pulmonary Arterial Hypertension
• 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
• 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
• 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)
• ECHINOSTOMA HORTENSE ASADA INFECTION IN THE DUODENUM : INCIDENTAL FINDINGS DURING ROUTINE GATROINTESTINAL ENDOSCOPY
• 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
• A Ten-Year Old Male with Bromocriptine Resistant PRL and GH-Producing Huge Pituitary Adenoma
• 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
• Stepped assessment of gastric emptying of a solid meal using the ^C-octanoic acid breath test
• Follow-Up Study of Children with Precocious Puberty Treated with Cyproterone Acetate
• Timing for Discontinuation of Treatment with a Long-Acting Gonadotropin-Releasing Hormone Analog in Girls with Central Precocious Puberty
• Consensus on Growth Hormone Treatment in Growth Hormone Deficient Children
• Efficacy of Recombinant Human Growth Hormone in Pediatric Renal Transplantation Patients after Withdrawal of Steroid Therapy:Report of Two Cases
• Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
• High-performance liquid chromatographic determination of lipoamidase (lipoyl-X hydrolase) activity with a novel substrate, lipoyl-6-aminoquinoline
• Nutrition Related Hormonal Changes in Obese Children
• Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene
• Combined GH and LHRH Analog Treatment in Short Children
• Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism
• Determination of biotin (vitamin H) by the high-performance affinity chromatography with a trypsin-treated avidin-bound column
• Protein determination by high-performance gel-permeation chromatography : applications to human pancreatic juice, human bile and tissue homogenate
• Serum protein determination by high-performance gel-permeation chromatography
• Comparison of Bone Age Estimation Methods : Computer Aided Skeletal Assessment System and Tanner-Whitehouse 2 Method Standardized for Japanese Children in Patients with Non-Endocrine Short Stature
• Pathophysiology underlying irritable bowel syndrome -From the viewpoint of dysfunction of autonomic nervous system activity-

もっと見る 閉じる

スポンサーリンク