Fujieda K | Division Of Endocrinology And Metabolism Osaka City General Hospital

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著作論文

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
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
Pharmacokinetics and Metabolic Effects of High-Dose Growth Hormone Administration in Healthy Adult Men
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
Registration System for Growth Hormone (GH) Treatment with Standardized Immunoreactive GH Values in Japan
Low-dose Growth Hormone Treatment (0.175mg/kg/week) for Short Stature in Patients with Turner Syndrome : Data from KIGS Japan
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
Growth Hormone (GH) Binding Protein in Children with Intrauterine Growth Retardation Treated with High Dose GH
Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
Two Novel Mutations in the Thyroid Peroxidase Gene with Goitrous Hypothyroidism
Height Responses in Complete ldiopathic Growth Hormone Deficient Children Less Than Three Years of Age during Growth Hormone Therapy
Growth-Promoting and Psychological Effects of High-Dose Growth Hormone Treatment in Children with Intrauterine Growth Retardation
Spontaneous Growth in Hormone-Treated Short Children
Growth Response to Growth Hormone Therapy in Patients with Different Degrees of Growth Hormone Deficiency
Clinical Outcome of GH Treatment in Turner Girls in Japan : Results of Multicentre Trial
Timing for Discontinuation of Treatment with a Long-Acting Gonadotropin-Releasing Hormone Analog in Girls with Central Precocious Puberty
Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism
Clinical characteristics of Japanese adults with growth hormone deficiency : a HypoCCS database study

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