Search Results1-13 of  13

  • KAMASAKI Hotaka ID: 9000001204683

    Department of Pediatrics, Tonan Hospital (2002 from CiNii)

    Articles in CiNii:1

    • A Girl with Turner Syndrome and Early Puberty : A Case Report (2002)
  • KAMASAKI Hotaka ID: 9000001495233

    Department of Pediatrics, Sapporo Medical University (2010 from CiNii)

    Articles in CiNii:2

    • Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia (2005)
    • Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies (2010)
  • KAMASAKI Hotaka ID: 9000014168413

    Department of Pediatrics, Sapporo Medical University School of Medicine (2008 from CiNii)

    Articles in CiNii:1

    • A significant improvement in lower limb pain after treatment with alendronate in two cases of Camurati-Engelmann disease (2008)
  • KAMASAKI Hotaka ID: 9000107396614

    Department of Pediatrics, Sapporo Medical University School of Medicine (2012 from CiNii)

    Articles in CiNii:1

    • Investigation of iodine deficient state and iodine supplementation in patients with severe motor and intellectual disabilities on long-term total enteral nutrition (2012)
  • KAMASAKI Hotaka ID: 9000265572018

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

    Articles in CiNii:1

    • A Case of Graves' Disease Diagnosed in the Course of Bilateral Carotid Artery Stenoses (Moyamoya Disease) ; A Case Report and Review of the Literature (2013)
  • KAMASAKI Hotaka ID: 9000265572180

    Department of Pediatrics, Sapporo Medical University, School of Medicine (2011 from CiNii)

    Articles in CiNii:1

    • Treatment of Hypothyroidism due to Iodine Deficiency Using Daily Powdered Kelp in Patients Receiving Long-term Total Enteral Nutrition (2011)
  • Kamasaki Hotaka ID: 9000257754501

    Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan (1998 from CiNii)

    Articles in CiNii:1

    • Central Hypothyroidism with Severely Delayed Myelination in a Boy Born to a Mother with Untreated Graves’ Disease (1998)
  • Kamasaki Hotaka ID: 9000257805648

    Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo 060-8543, Japan|Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo 060-8543, Japan (2012 from CiNii)

    Articles in CiNii:1

    • Investigation of iodine deficient state and iodine supplementation in patients with severe motor and intellectual disabilities on long-term total enteral nutrition (2012)
  • Kamasaki Hotaka ID: 9000309180759

    Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan (2015 from CiNii)

    Articles in CiNii:1

    • An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the <i>CDC73</i> gene (2015)
  • Kamasaki Hotaka ID: 9000345378535

    Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan (2017 from CiNii)

    Articles in CiNii:1

    • A novel heterozygous intronic mutation in <i>POU1F1</i> is associated with combined pituitary hormone deficiency (2017)
  • Kamasaki Hotaka ID: 9000367422594

    Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan|The Committee on Mass Screening of the Japanese Society for Pediatric Endocrinology (2017 from CiNii)

    Articles in CiNii:1

    • Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in Japan (2017)
  • Kamasaki Hotaka ID: 9000380968861

    Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan (2018 from CiNii)

    Articles in CiNii:1

    • Adrenocortical carcinoma characterized by gynecomastia: A case report (2018)
  • Kamasaki Hotaka ID: 9000402249775

    Department of Pediatrics, Sapporo Medical University School of Medicine, Hokkaido 060-8543, Japan (2019 from CiNii)

    Articles in CiNii:1

    • Language delay and developmental catch-up would be a clinical feature of pseudohypoparathyroidism type 1A during childhood (2019)
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