バックナンバー:Clinical Pediatric Endocrinology

Clinical Pediatric Endocrinology
25巻 3号

  • Efficacy of single serum cortisol reading obtained between 9 AM and 10 AM as an index of adrenal function in children treated with glucocorticoids or synthetic adrenocorticotropic hormone

    Masahiro Goto, Nao Shibata, Yukihiro Hasegawa
    Division of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center
    Clinical Pediatric Endocrinology 25(3): 83-89, 2016.


    アブストラクト】 従量制は110円(税込)、基本料金制は基本料金に含まれます
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  • Potential utility of cinacalcet as a treatment for CDC73-related primary hyperparathyroidism : a case report

    Takeshi Sato1,2, Koji Muroya1, Junko Hanakawa1, Sumimasa Yamashita3, Kumiko Nozawa4, Katsuhiko Masudo5, Tadashi Yamakawa6, Yumi Asakura1, Tomonobu Hasegawa2, Masanori Adachi1
    1Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, 2Department of Pediatrics, Keio University School of Medicine, 3Department of Child Neurology, Kanagawa Children's Medical Center, 4Department of Radiology, Kanagawa Children's Medical Center, 5Department of Breast and Thyroid Surgery, Yokohama City University Medical Center, 6Department of Endocrinology and Diabetes, Yokohama City University Medical Center
    Clinical Pediatric Endocrinology 25(3): 91-98, 2016.


    アブストラクト】 従量制は110円(税込)、基本料金制は基本料金に含まれます
    全文ダウンロード(6.80MB)】 従量制、基本料金制の方共に660円(税込) です。

  • Chromosome 6q24 methylation defects are uncommon in childhood-onset non-autoimmune diabetes mellitus patients born appropriate- or large-for-gestational age

    Misako Okuno1,2, Tohru Yorifuji3, Masayo Kagami1, Tadayuki Ayabe1, Tatsuhiko Urakami2, Tomoyuki Kawamura4, Nobuyuki Kikuchi5, Ichiro Yokota6, Toru Kikuchi7, Shin Amemiya7, Junichi Suzuki2, Tsutomu Ogata1,8, Shigetaka Sugihara9, Maki Fukami1, The Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT)
    1Departments of Molecular Endocrinology, National Research Institute for Child Health and Development, 2Department of Pediatrics and Child Health, Nihon University School of Medicine, 3Department of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, 4Department of Pediatrics, Osaka City University, 5Department of Pediatrics, Yokohama City Minato Red Cross Hospital, 6Department of Pediatrics, Division of Pediatric Endocrinology and Metabolism, Shikoku Medical Center for Children and Adults, 7Department of Pediatrics, Saitama Medical University, 8Department of Pediatrics, Hamamatsu University School of Medicine, 9Department of Pediatrics, Tokyo Women's Medical University Medical Center East
    Clinical Pediatric Endocrinology 25(3): 99-102, 2016.


    アブストラクト】 従量制は110円(税込)、基本料金制は基本料金に含まれます
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  • A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3

    Keiko Nagahara1,2, Yuki Harada3, Tohru Futami3, Masaki Takagi1,4, Gen Nishimura5, Yukihiro Hasegawa1
    1Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, 2Department of Pediatrics, Showa University School of Medicine, 3Department of Orthopedic Surgery, Shiga Medical Center for Children, 4Department of Pediatrics, Keio University School of Medicine, 5Department of Radiology, Tokyo Metropolitan Children's Medical Center
    Clinical Pediatric Endocrinology 25(3): 103-106, 2016.


    アブストラクト】 従量制は110円(税込)、基本料金制は基本料金に含まれます
    全文ダウンロード(3.83MB)】 従量制、基本料金制の方共に660円(税込) です。

  • A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1

    Shinji Higuchi1, Masaki Takagi1,2, Satoshi Shimomura3, Gen Nishimura4, Yukihiro Hasegawa1,2
    1Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, 2Department of Pediatrics, Keio University School of Medicine, 3Department of Orthopedics, Tokyo Metropolitan Children's Medical Center, 4Department of Radiology, Tokyo Metropolitan Children's Medical Center
    Clinical Pediatric Endocrinology 25(3): 107-110, 2016.


    アブストラクト】 従量制は110円(税込)、基本料金制は基本料金に含まれます
    全文ダウンロード(3.28MB)】 従量制、基本料金制の方共に660円(税込) です。

  • A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1

    Toshiki Tsunogai1, Ichiro Miyata2, Saori Kotake1, Ryuki Matsuura1, Ken Takagi1, Hiroyuki Nanba1, Noriko Takahata1, Toshihiro Tajima3, Yasuyuki Wada1
    1Department of Pediatrics, The Jikei University Kashiwa Hospital, 2Department of Pediatrics, The Jikei University School of Medicine, 3Jichi Children's Medical Center Tochigi
    Clinical Pediatric Endocrinology 25(3): 111-114, 2016.


    アブストラクト】 従量制は110円(税込)、基本料金制は基本料金に含まれます
    全文ダウンロード(3.46MB)】 従量制、基本料金制の方共に660円(税込) です。

  • A novel frameshift mutation in the TRPS1 gene caused Tricho-rhino-phalangeal syndrome type I and III in a Japanese family

    Masatsune Itoh1,2, Yuko Kittaka1, Yo Niida2, Yutaka Saikawa1
    1Department of Pediatrics, Kanazawa Medical University, 2Division of Clinical Genetics, Multidisciplinary Medical Center, Kanazawa Medical University Hospital
    Clinical Pediatric Endocrinology 25(3): 115-118, 2016.


    アブストラクト】 従量制は110円(税込)、基本料金制は基本料金に含まれます
    全文ダウンロード(3.25MB)】 従量制、基本料金制の方共に660円(税込) です。

book
発行元:
日本小児内分泌学会
ISSN:
0918-5739
ISSN(オンライン):
1347-7358

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