Search Results1-11 of  11

  • ARIYASU Daisuke ID: 9000001710382

    Endocrinology and Metabolism Unit, Tokyo Metropolitan Kiyose Children's Hospital (2006 from CiNii)

    Articles in CiNii:1

    • Genetic and enzymatic analysis for two Japanese patients with idiopathic infantile arterial calcification (2006)
  • ARIYASU Daisuke ID: 9000265572422

    Department of Endocrinology and Metabolism, Tokyo Metropolitan Kiyose Children's Hospital (2009 from CiNii)

    Articles in CiNii:1

    • Patients with Hypophosphatemic Osteomalacia Need Continuous Treatment during Adulthood (2009)
  • ARIYASU Daisuke ID: 9000265572479

    Division of Endocrinology and Metabolism, Tokyo Metropolitan Kiyose Children's Hospital (2008 from CiNii)

    Articles in CiNii:1

    • The Range of 2.2-3.3 mg/gCr of Pregnanetriol in the First Morning Urine Sample as an Index of Optimal Control in CYP21 Deficiency (2008)
  • ARIYASU Daisuke ID: 9000348582240

    Division of Endocrinology and Metabolism, Tokyo Metropolitan Children's Hospital (2011 from CiNii)

    Articles in CiNii:3

    • Serum FSH level below 10mIU/mL at twelve years old is an index of spontaneous and cyclical menstruation in Turner syndrome (2010)
    • High iFGF23 level despite hypophosphatemia is one of the clinical indicators to make diagnosis of XLH (2011)
    • Pregnanetriol in the Range of 1.2-2.1mg/m^2/day as an Index of Optimal Control in CYP21A2 Deficiency (2007)
  • ARIYASU Daisuke ID: 9000364875358

    Department of Pediatrics, Keio University School of Medicine (2013 from CiNii)

    Articles in CiNii:13

    • Osteoporosis during childhood (2005)
    • 従来報告のないWT1遺伝子異常を呈した巣状分節性糸球体硬化症の1例 (2006)
    • Review : Hypophosphatemic rickets/osteomalacia (2009)
  • Ariyasu Daisuke ID: 9000257803812

    Endocrinology and Metabolism Division, Tokyo Metropolitan Children’s Medical Center, Tokyo, Japan (2010 from CiNii)

    Articles in CiNii:1

    • Serum FSH level below 10 mIU/mL at twelve years old is an index of spontaneous and cyclical menstruation in Turner syndrome (2010)
  • Ariyasu Daisuke ID: 9000257804978

    Division of Endocrinology and Metabolism, Tokyo Metropolitan Children’s Hospital, Tokyo 183-8561, Japan (2011 from CiNii)

    Articles in CiNii:1

    • High iFGF23 level despite hypophosphatemia is one of the clinical indicators to make diagnosis of XLH (2011)
  • Ariyasu Daisuke ID: 9000322102190

    Division of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan (2016 from CiNii)

    Articles in CiNii:1

    • Early-onset urological disorders due to Wolfram syndrome: A case of neonatal onset (2016)
  • Ariyasu Daisuke ID: 9000345378549

    Division of Endocrinology and Metabolism, Tokyo Metropolitan Children’s Medical Center, Tokyo, Japan (2017 from CiNii)

    Articles in CiNii:1

    • Gradually increasing ethinyl estradiol for Turner syndrome may produce good final height but not ideal BMD (2017)
  • Ariyasu Daisuke ID: 9000345429606

    Division of Developmental Genetics, Institute of Resource Development and Analysis, Kumamoto University, Kumamoto, Japan (2016 from CiNii)

    Articles in CiNii:1

    • A case of transient neonatal diabetes due to a novel mutation in <i>ABCC8</i> (2016)
  • Ariyasu Daisuke ID: 9000367422429

    Division of Developmental Genetics, Institute of Resource Development and Analysis, Kumamoto University, Kumamoto, Japan (2017 from CiNii)

    Articles in CiNii:1

    • A Japanese boy with fructose-1,6-bisphosphatase deficiency who had a novel <i>FBP1</i> mutation (p.Phe90Val) (2017)
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