Search Results1-14 of  14

  • FURUTANI Yoshiyuki ID: 9000003876274

    The Heart Institute of Japan, Tokyo Women's Medical University (2002 from CiNii)

    Articles in CiNii:6

    • Genetic analysis of familial long QT syndrome:Missense mutation in HERG in LQT2 family (1996)
    • Ductus Arteriosus and Oxygen:The Effect of Oxygen on the Expression of Smooth Muscle Myosin Heavy Chain mRNA Types (1995)
    • IS052 A mitochondrial DNA is responsible for the pathogenesis of congenital long QT syndrome (1999)
  • FURUTANI Yoshiyuki ID: 9000016186148

    Articles in CiNii:13

    • 平成17-19年度研究課題報告18および13トリソミーの心表現型・遺伝子型と予後 (2009)
    • 平成17-19年度研究課題報告無脾症, 多脾症における重症感染症の疫学 (2009)
    • 平成17-19年度研究課題報告 Williams 症候群の表現型-心疾患およびその他年齢別に注意すべき症状の頻度 (2009)
  • FURUTANI Yoshiyuki ID: 9000019067525

    Department of Pediatric Cardiology, Tokyo Women's Medical University (2012 from CiNii)

    Articles in CiNii:1

    • Missense Mutations of the BMPR1B (ALK6) Gene in Childhood Idiopathic Pulmonary Arterial Hypertension (2012)
  • FURUTANI Yoshiyuki ID: 9000021188557

    東京女子医科大学循環器小児科 (1999 from CiNii)

    Articles in CiNii:1

    • How to use DNA Information. (1999)
  • FURUTANI Yoshiyuki ID: 9000297500514

    Articles in CiNii:1

    • Therapeutic efficacy of valproic acid in a combined monocrotaline and chronic hypoxia rat model of severe pulmonary hypertension (2015)
  • FURUTANI Yoshiyuki ID: 9000403296017

    Articles in CiNii:1

    • Silibinin efficacy in a rat model of pulmonary arterial hypertension using monocrotaline and chronic hypoxia (2019)
  • Furutani Yoshiyuki ID: 9000021114568

    International Research and Educational Institute for Integrated Medical Science (IREIIMS), Tokyo Women's Medical University (2007 from CiNii)

    Articles in CiNii:1

    • Possibility of Integrated Data Mining of Clinical Data (2007)
  • Furutani Yoshiyuki ID: 9000021668376

    The Department of Pediatric Cardiology, Tokyo Women’s Medical University (2011 from CiNii)

    Articles in CiNii:1

    • Progression of Juvenile Atrial Standstill in a Boy with SCN5A Mutation (2011)
  • Furutani Yoshiyuki ID: 9000242071974

    Department of Pediatric Cardiology, Tokyo Women’s Medical University (2014 from CiNii)

    Articles in CiNii:1

    • Soluble ST2 and N-terminal pro-Brain Natriuretic Peptide Combination:– Useful Biomarker for Predicting Outcome of Childhood Pulmonary Arterial Hypertension – (2014)
  • Furutani Yoshiyuki ID: 9000283421265

    Committee for Genetics and Epidemiology of Cardiovascular Diseases, Japanese Society of Pediatric Cardiology and Cardiac Surgery (2013 from CiNii)

    Articles in CiNii:1

    • Clinical Characteristics of Brain Abscess in Cyanotic Congenital Heart Disease in Japan (2013)
  • Furutani Yoshiyuki ID: 9000312725119

    Department of Pediatric Cardiology, Tokyo Women's Medical University (2015 from CiNii)

    Articles in CiNii:1

    • Establishment and Characterization of Induced Pluripotent (iPS) Stem Cells Derived from Immortalized B Cells of Cardiac Channelopathy Patients (2015)
  • Furutani Yoshiyuki ID: 9000321638347

    Articles in CiNii:1

    • High prevalence of cardiovascular risk factors in children and adolescents with Williams-Beuren syndrome (2015)
  • Furutani Yoshiyuki ID: 9000323840987

    Tokyo Women's Medical University Hospital, Department of Pediatric Cardiology (2016 from CiNii)

    Articles in CiNii:1

    • A Pediatric Case of Arrhythmogenic Right Ventricular Cardiomyopathy (2016)
  • Yoshiyuki Furutani ID: 9000383207397

    Articles in CiNii:1

    • Analysis of Genetic Mutations Related to TGF-β/BMP Signaling in Children and Adults with Pulmonary Arterial Hypertension (2015)
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