Search Results - Saisho, Sumitaka

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  1. 1
    Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood

    Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood by KASHIMADA, Ken-ichi, ONO, Makoto, ONISHI, Toshikazu, KOYAMA, Satimi, TOYOURA, Takio, IMAI, Kazuhide, SAISHO, Sumitaka, MIZUTANI, Shuki

    Published in Endocrine Journal
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  2. 2
    Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood

    Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood by KEN-ICHI KASHIMADA, MAKOTO ONO, TOSHIKAZU ONISHI, SATIMI KOYAMA, TAKIO TOYOURA, KAZUHIDE IMAI, SUMITAKA SAISHO, SHUKI MIZUTANI

    Published in ENDOCRINE JOURNAL
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  3. 3
    Genetic Analysis of Japanese Patients with 21-Hydroxylase Deficiency: Identification of a Patient with a New Mutation of a Homozygous Deletion of Adenine at Codon 246 and Patients without Demonstrable Mutations within the Structural Gene for CYP21

    Genetic Analysis of Japanese Patients with 21-Hydroxylase Deficiency: Identification of a Patient with a New Mutation of a Homozygous Deletion of Adenine at Codon 246 and Patients... by Koyama, Satomi, Toyoura, Takio, Saisho, Sumitaka, Shimozawa, Kazuhiko, Yata, Junichi

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  4. 4
    Genetic analysis of Japanese patients with 21-hydroxylase deficiency: Identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients without demonstrable mutations within the structural gene for CYP21 : The impact of the human genome on endocrinology: Special features

    Genetic analysis of Japanese patients with 21-hydroxylase deficiency: Identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients... by KOYAMA, Satomi, TOYOURA, Takio, SAISHO, Sumitaka, SHIMOZAWA, Kazuhiko, YATA, Junichi

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  5. 5
    A highly specific heterologous enzyme immunoassay for 5α-androstane-3α, 17β-diol 17-glucuronide (androstanediol-17G) and developmental patterns of urinary androstanediol-17G excretions

    A highly specific heterologous enzyme immunoassay for 5α-androstane-3α, 17β-diol 17-glucuronide (androstanediol-17G) and developmental patterns of urinary androstanediol-17G excret... by Onishi, Toshikazu, Takei, Hajime, Kambegawa, Akira, Saisho, Sumitaka, Kashimada, Kenichi, Koyama, Satomi, Mizutani, Shuki, Rao, Pemmaraju N.

    Published in Steroids
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  6. 6
    A highly specific heterologous enzyme immunoassay for 5 alpha-androstane-3 alpha, 17 beta-diol 17-glucuronide (androstanediol-17G) and developmental patterns of urinary androstanediol-17G excretions

    A highly specific heterologous enzyme immunoassay for 5 alpha-androstane-3 alpha, 17 beta-diol 17-glucuronide (androstanediol-17G) and developmental patterns of urinary androstaned... by Onishi, Toshikazu, Takei, Hajime, Kambegawa, Akira, Saisho, Sumitaka, Kashimada, Kenichi, Koyama, Satomi, Mizutani, Shuki, Rao, Pemmaraju N

    Published in Steroids
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