All Stories

  1. Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene

    Article • Clinical Pediatric Endocrinology, January 2015, Japanese Society for Pediatric Endocrinology

    Dr Kosei Hasegawa, Dr Kosei Hasegawa

  2. Children with short-limbed short stature in pediatric endocrinological services in Japan

    Article • Pediatrics International, November 2014, Wiley

    Dr Kosei Hasegawa, Dr Kosei Hasegawa

  3. Fibroblast growth factor 23 concentrations in healthy term infants during the early postpartum period

    Article • Bone, August 2010, Elsevier

    Dr Kosei Hasegawa, Dr Kosei Hasegawa

  4. Urinary N‐telopeptides of type I collagen in healthy children

    Article • Pediatrics International, June 2010, Wiley

    Dr Kosei Hasegawa, Dr Kosei Hasegawa

  5. Growth of infants with osteogenesis imperfecta treated with bisphosphonate

    Article • Pediatrics International, February 2009, Wiley

    Dr Kosei Hasegawa, Dr Kosei Hasegawa

  6. Late-onset Lymphedema and Protein-losing Enteropathy with Noonan Syndrome

    Article • Clinical Pediatric Endocrinology, January 2009, Japanese Society for Pediatric Endocrinology

    Dr Kosei Hasegawa, Dr Kosei Hasegawa

  7. Impaired pyridinoline cross-link formation in patients with osteogenesis imperfecta

    Article • Journal of Bone and Mineral Metabolism, July 2008, Springer Science + Business Media

    Dr Kosei Hasegawa, Dr Kosei Hasegawa

  8. Mutations in type I collagen genes in Japanese osteogenesis imperfecta patients

    Article • Pediatrics International, July 2007, Wiley

    Dr Kosei Hasegawa, Dr Kosei Hasegawa