Katsumata Noriyuki | Department Of Endocrinology & Metabolism National Children's Medical Research Center

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著作論文

Serum Levels of Free Insulin-Like Growth Factor (IGF)-I in Normal Children
Determination of specific activities and kinetic constants of biotinidase and lipoamidase in LEW rat and Lactobacillus casei (Shirota)
CD44 Variant Isoform Expression and Breast Cancer Prognosis
Unknown primary carcinoma: a feasibility assessment of combination chemotherapy with cisplatin and docetaxel
Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome
Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan
Replacement of Alanine with Asparagic Acid at Position 203 in Human Steroidogenic Acute Regulatory Protein Impairs the Ability to Enhance Steroidogenesis in vitro
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)
Hypospadias in a Male Patient with 21-hydroxylase Deficiency
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
HER2 Is Frequently Over-expressed in Ovarian Clear Cell Adenocarcinoma : Possible Novel Treatment Modality Using Recombinant Monoclonal Antibody against HER2, Trastuzumab
U7 snRNA-mediated correction of aberrant splicing caused by activation of cryptic splice sites
Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
Long Term Follow-Up of a 46,XY Phenotypic Girl with 17α-Hydroxylase Deficiency Treated with Alternate-Day Dexamethasone
Measuring Quality of Life in Patients with Breast Cancer: A Systematic Review of Reliable and Valid Instruments Available in Japan
Systematic Overview of Quality of Life Studies for Breast Cancer
Cholesterol Side-Chain Cleavage Enzyme (SCC) Deficiency
Sibling Cases of Addisons Disease Caused byDAX-1 Gene Mutations
Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene
Analysis of the AAAS Gene in a Japanese Patient with Triple A Syndrome
Evidence-based guidelines for treatment of uterine body neoplasm in Japan : Japan Society of Gynecologic Oncology (JSGO) 2009 edition
Determination of biotin (vitamin H) by the high-performance affinity chromatography with a trypsin-treated avidin-bound column
Multicenter, phase II, placebo-controlled, double-blind, randomized study of aprepitant in Japanese patients receiving high-dose cisplatin
Selective Amplification of Exons 3 and 8 of the Human Growth Hormone Receptor (hGHR) Gene Based on Newly Identified Intron Sequences
Response to Paulo et al. : Japanese patients equally likely to benefit from aprepitant for chemotherapy-induced nausea and vomiting prevention
Novel C617Y mutation in the 7th transmembrane segment of luteinizing hormone/choriogonadotropin receptor in a Japanese boy with peripheral precocious puberty

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