Hasegawa Y | Department Of Laboratory Medicine Osaka University Medical School

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概要

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著作論文

Identification and characterization of cryptic SHOX intragenic deletions in three Japanese patients with Leri-Weill dyschondrosteosis
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
MEN1 Gene Analysis in Patients with Primary Hyperparathyroidism : 10-year Experience of a Single Institution for Thyroid and Parathyroid Care in Japan
BRAF Mutation in Papillary Thyroid Carcinoma in a Japanese Population : Its Lack of Correlation with High-Risk Clinicopathological Features and Disease-Free Survival of Patients
Y-box binding protein expression in thyroid neoplasms : Its linkage with anaplastic transformation
Statural Growth in 31 Japanese Patients with SHOX Haploinsufficiency : Support for a Disadvantageous Effect of Gonadal Estrogens
Prevalence of TSH Receptor and Gsα Mutations in 45 Autonomously Functioning Thyroid Nodules in Japan
Large-scale Analysis of Mutations in RET Exon 16 in Sporadic Medullary Thyroid Carcinomas in Japan
A Case of Repeated Painless Thyroiditis Followed by Graves' Disease
Quantitative Analysis of Osteonectin mRNA in Thyroid Carcinomas
Self-Examination of Thyroid Nodules
Increased Free Form of Insulin-Like Growth Factor-I in Circulation throughout Normal Human Pregnancy
Clinical Utility of Insulin-Like Growth Factor-l(IGF-I)and IGF Binding Protein-3 Levels in the Diagnosis of GH Deficiency(GHD)During Childhood
Practical Treatment with Minimum Maintenance Dose of Anti-Thyroid Drugs for Prediction of Remission in Graves' Disease
Blocking Type Anti-TSH Receptor Antibodies Detected by Radioreceptor Assay in Graves' Disease
Mutational Analysis of Androgen Receptor (AR) Gene in 46, XY Patients with Ambiguous Genitalia and Normal Testosterone Secretion : Endocrinological Characteristics of Three Patients with AR Gene Mutations
A Novel Thyrotropin Receptor Germline Mutation (Asp617Tyr) Causing Hereditary Hyperthyroidism
A Case of Congenital Hypopituitarism: Difficulty in the Diagnosis of ACTH Deficiency Due to High Serum Cortisol Levels from a Hypothyroid State
Abosence of Proteolysis of lnsulin-like Growth Factor Binding Protein-3 in Serum from Patients with Growth Hormone Deficiency
Increase in Free Insulin-Like Growth Factor-I Levels in Precocious and Normal Puberty
Proteolytic Activity of IGFBP-3 in Various Clinical Conditions During Childhood Studied by Means of Western Immunoblotting
Development of Growth Hormone and Adrenocorticotropic Hormone Deficiencies in Patients with Prenatal or Perinatal-Onset Hypothalamic Hypopituitarism Having Invisible or Thin Pituitary Stalk on Magnetic Resonance Imaging
Encapsulated Anaplastic Thyroid Carcinoma Without Invasive Phenotype with Favorable Prognosis : Report of a Case
Expression of cdc25A and cdc25B Phosphatase in Breast Carcinoma
Long-Term Effects of Thyroid Hormone on Lymphocyte Subsets in Spleens and Thymuses of Mice
Significance of Thyroid Stimulating Antibody and Long Term Follow Up in Patients with Euthyroid Grave's Disease
Thrombospondin 1 mRNA as a Candidate for a Marker to Detect Thyroid-derived Fibroblasts in Fine Needle Aspiration Biopsy of the Thyroid
Hashimoto's Disease and Dr. Hakaru Hashimoto

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