Search Results1-10 of  10

  • MATSUO Kumihiro ID: 9000015644618

    Articles in CiNii:2

    • Detection of Heterozygous Familial Hypercholesterolemia by Serum Lipid Profile Screening in Children Hospitalized at Furano Hospital, Japan (2019)
    • Newborn hearing screening using distortion product otoacoustic emissions (DPOAE) in Furano City (2003)
  • MATSUO Kumihiro ID: 9000018779576

    Department of Pediatrics, Asahikawa Medical College (2010 from CiNii)

    Articles in CiNii:1

    • Unilateral adrenalectomy can be an alternative therapy for infantile onset Cushing's syndrome caused by ACTH-independent macronodular adrenal hyperplasia with McCune-Albright syndrome (2010)
  • MATSUO Kumihiro ID: 9000364845124

    Articles in CiNii:7

    • McCune-Albright syndrome successfully treated with methimazole and cabergoline (2010)
    • 代謝 単純性肥満 (ミニ特集 ここまで分かる成長曲線) (2007)
    • ビタミンD欠乏症 (ミニ特集 内分泌・代謝疾患の診断と治療Update) (2009)
  • Matsuo Kumihiro ID: 9000020184526

    Department of Pediatrics, Asahikawa Medical University (2011 from CiNii)

    Articles in CiNii:1

    • Evaluation of steroid absorption with measurement of urinary free cortisol n a case of short bowel syndrome with membranoproliferative glomerulonephritis (2011)
  • Matsuo Kumihiro ID: 9000024422236

    Articles in CiNii:1

    • Permanent Neonatal Diabetes Mellitus with Growth Disturbance,Developmental Delay,Epilepsy and Dysmorphic Features (2005)
  • Matsuo Kumihiro ID: 9000257753862

    Department of Pediatrics, Asahikawa Medical College (2005 from CiNii)

    Articles in CiNii:1

    • Permanent Neonatal Diabetes Mellitus with Growth Disturbance, Developmental Delay, Epilepsy and Dysmorphic Features (2005)
  • Matsuo Kumihiro ID: 9000257804284

    Department of Pediatrics, Asahikawa Medical College, Asahikawa, Japan (2010 from CiNii)

    Articles in CiNii:1

    • Unilateral adrenalectomy can be an alternative therapy for infantile onset Cushing' s syndrome caused by ACTHindependent macronodular adrenal hyperplasia with McCune-Albright syndrome (2010)
  • Matsuo Kumihiro ID: 9000283362869

    Department of Pediatrics, Asahikawa Medical College, Asahikawa, Japan (2013 from CiNii)

    Articles in CiNii:1

    • A Case of Vitamin D Deficiency without Elevation of Serum Alkaline Phosphatase in a Carrier of Hypophosphatasia (2013)
  • Matsuo Kumihiro ID: 9000367422635

    Department of Pediatrics, Asahikawa Medical University, Hokkaido, Japan (2017 from CiNii)

    Articles in CiNii:1

    • Novel splice site mutation in <i>GATA3</i> in a patient with HDR syndrome (2017)
  • Matsuo Kumihiro ID: 9000398406163

    Articles in CiNii:1

    • Four Japanese Patients with Congenital Nephrogenic Diabetes Insipidus due to the AVPR2 Mutations (2018)
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