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Department Of Pediatrics Asahikawa Medical College | 論文
- A Japanese Patient of Congenital Hypothyroidism with Cerebellar Atrophy
- 34 NOVEL MUTATIONS IN THE CYP11B1 GENE IN JAPANESEPATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA DUE TO 11β-HYDROXYIASE DEFICIENCY
- 52 STUDIES OF HEPATOCYTE NUCLER FACTER-4α HNF4-α AND HNF-1β GENES IN JUVENILE ONSET DIABETES MELLITUS WITHOUT OBESITY
- Haplotype analysis of the human collectin placenta 1 (hCL-P1) gene
- Monozygotic Twins with Discordant Sexual Phenotypes due to Different Rations of Mosaicism of 47, X, idic(Y), idic(Y)/46, X, idic(Y)/45, X
- Pharmacokinetics and Metabolic Effects of High-Dose Growth Hormone Administration in Healthy Adult Men
- Modified Atkins diet therapy for a case with glucose transporter type 1 deficiency syndrome
- 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
- Familial hypomagnesemia with hypercalciuria and nephrocalcinosis : unusual clinical associations and novel claudin16 mutation in an Egyptian family
- 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
- 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