Search Results1-20 of  84

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  • Ozono Keiichi ID: 9000403878039

    Articles in CiNii:1

    • Systematic Cellular Disease Models Reveal Synergistic Interaction of Trisomy 21 and GATA1 Mutations in Hematopoietic Abnormalities (2016)
  • Ozono Keiichi ID: 9000409323948

    Articles in CiNii:1

    • Effect of growth hormone (GH) treatment on adult height in patients with GH deficiency : the Japanese cohort from the GeNeSIS observational study (2020)
  • Keiichi Ozono ID: 9000348573031

    Articles in CiNii:1

    • 136 Excessive Growth in a Japanese Girl with Weaver Syndrome (2002)
  • Keiichi Ozono ID: 9000348581246

    Articles in CiNii:1

    • Longitudinal Observation of a Patient with Leri-Weill Dyschondrosteosis and SHOX Haploinsufficiency (2005)
  • Keiichi Ozono ID: 9000406382389

    Articles in CiNii:1

    • Elimination of protein aggregates prevents premature senescence in human trisomy 21 fibroblasts (2019)
  • OZONO KEIICHI ID: 9000252825156

    Department of Environmental Medicine, Osaka Medical Center and Research Institute for Maternal and Child Health (2001 from CiNii)

    Articles in CiNii:1

    • Hyperintensity of Posterior Pituitary on MR T1WI in a Boy with Central Diabetes Insipidus Caused by Missense Mutation of Neurophysin II Gene. (2001)
  • OZONO Keiichi ID: 1000020270770

    Department of Pediatrics, Osaka University Graduate School of Medicine (2011 from CiNii)

    Articles in CiNii:44

    • Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia (2000)
    • The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets (1996)
    • Hyperintensity of Posterior Pituitary on MR T1WI in a Boy with Central Diabetes Insipidus Caused by Missense Mutation of Neurophysin II Gene (2001)
  • OZONO Keiichi ID: 9000000504815

    Department of Environmental Medicine, Osaka Medical Center and Research Institute for Maternal and Child Health (1999 from CiNii)

    Articles in CiNii:1

    • Analysis of the stable levels of messenger RNA derived from different polymorphic alleles in the vitamin D receptor gene (1999)
  • OZONO Keiichi ID: 9000001461305

    Department of Pediatrics, Osaka University Graduate School of Medicine (2005 from CiNii)

    Articles in CiNii:1

    • Epilepsy in Wolf-Hirschhorn Syndrome (4p-) (2005)
  • OZONO Keiichi ID: 9000001610265

    Department of pediatrics, Osaka University Graduate School of Medicine (2004 from CiNii)

    Articles in CiNii:1

    • Phenotype and genotype analysis of severe skeletal dysplasia (2004)
  • OZONO Keiichi ID: 9000014168166

    Department of Pediatrics, Osaka University Graduate School of Medicine (2007 from CiNii)

    Articles in CiNii:1

    • Genetic association of a polymorphism of the cAMP-responsive element binding protein-binding protein with steroid-induced osteonecrosis after kidney transplantation (2007)
  • OZONO Keiichi ID: 9000014174135

    Department of Pediatrics, Osaka University, Graduate School of Medicine (2008 from CiNii)

    Articles in CiNii:1

    • Hepatitis C virus infection and interferon therapy in patients with Down syndrome (2008)
  • OZONO Keiichi ID: 9000016421093

    Department of Pediatrics, Osaka University Graduate School of Medicine (2009 from CiNii)

    Articles in CiNii:1

    • Wnt signaling in bone metabolism (2009)
  • OZONO Keiichi ID: 9000018652187

    Department of Pediatrics, Osaka University Graduate School of Medicine (2009 from CiNii)

    Articles in CiNii:1

    • Risk factors for neurological complications in complete hemolytic uremic syndrome caused by Escherichia coli O157 (2009)
  • OZONO Keiichi ID: 9000019147312

    Department of Pediatrics Osaka University Graduate School of Medicine (2011 from CiNii)

    Articles in CiNii:1

    • Hypophosphatasia now draws more attention of both clinicians and researchers : A Commentary on prevelance of c. 1559deIT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasias in Japanese and effects of the mutation on heterozygous carriers (2011)
  • OZONO Keiichi ID: 9000107310945

    Department of Developmental Medicine (Pediatrics), Osaka University Graduate School of Medicine (2012 from CiNii)

    Articles in CiNii:1

    • Clinicogenetical features of a Japanese patient with giant axonal neuropathy (2012)
  • OZONO Keiichi ID: 9000248229764

    Department of Pediatrics, Osaka University Graduate School of Medicine (2011 from CiNii)

    Articles in CiNii:1

    • Major role of apolipoprotein B in cycloheximide-induced acute hepatic steatosis in mice (2011)
  • OZONO Keiichi ID: 9000256892739

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

    Articles in CiNii:1

    • An observational study of the effectiveness and safety of growth hormone (Humatrope^【○!R】) treatment in Japanese children with growth hormone deficiency or Turner syndrome (2013)
  • OZONO Keiichi ID: 9000257801522

    Department of Developmental Medicine, Pediatrics, Osaka University Graduate School of Medicine (2006 from CiNii)

    Articles in CiNii:1

    • Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome (2006)
  • OZONO Keiichi ID: 9000257802997

    Department of Pediatrics, Osaka University Graduate School of Medicine (2008 from CiNii)

    Articles in CiNii:1

    • Causes and Differential Diagnosis of Hypocalcemia -Recommendation Proposed by Expert Panel Supported by Ministry of Health, Labour and Welfare, Japan- (2008)
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