Fujieda K | Dep. Of Pediatrics Asahikawa Medical Coll. Asahikawa Jpn

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概要

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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 Japanese Patient of Congenital Hypothyroidism with Cerebellar Atrophy
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
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
Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
Two Novel Mutations in the Thyroid Peroxidase Gene with Goitrous Hypothyroidism
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
Clinical characteristics of Japanese adults with growth hormone deficiency : a HypoCCS database study

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