Search Results1-9 of  9

  • FUKUZAWA Ryuji ID: 9000000412074

    Department of Pathology, Keio University School of Medicine (2000 from CiNii)

    Articles in CiNii:1

    • A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilm's Tumors^1 (2000)
  • FUKUZAWA Ryuji ID: 9000001051558

    慶應義塾大学医学部小児科 (1996 from CiNii)

    Articles in CiNii:2

    • A Case of Post-Traumatic Liver Abscess (1995)
    • Experience of Long-term and Small Dose of Erythromycin to Pediatric Patients with Tracheotomy (1996)
  • FUKUZAWA Ryuji ID: 9000003507955

    東京都立小児総合医療センター検査科 (2012 from CiNii)

    Articles in CiNii:9

    • Report on 5 cases of pediatric adrenocortical carcinoma (2010)
    • 7. CA 19-9 の上昇を認めた脾腫瘍の 1 例(第 12 回日本小児脾臓研究会) (2000)
    • PS-058 気管支閉鎖症44例の臨床病理学的検討(頚・胸部疾患治療の最前線,ポスターシンポジウム,病気の子供達に笑顔 小児外科に夢そして革新を,第47回 日本小児外科学会学術集会) (2010)
  • FUKUZAWA Ryuji ID: 9000265563069

    Department of Pathology and Laboratory Medicine, Tokyo Metropolitan Children's Medical Center (2013 from CiNii)

    Articles in CiNii:1

    • A Case of Cardiac Fibroma Diagnosed after Cardiopulmonary Arrest (2013)
  • Fukuzawa Ryuji ID: 9000253180392

    Department of Pathology, Keio University School of Medicine (2000 from CiNii)

    Articles in CiNii:1

    • A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors. (2000)
  • Fukuzawa Ryuji ID: 9000265536903

    Department of Pathology, Tokyo Metropolitan Children's Medical Center (2014 from CiNii)

    Articles in CiNii:1

    • Pathological Analysis of Pulmonary Cystic Lesions in Bronchial Atresia: Congenital Cystic Adenomatoid Malformation is a Developmental Abnormality Associated With Fetal Airway Obstruction (2014)
  • Fukuzawa Ryuji ID: 9000345378537

    Department of Pathology and Laboratory Medicine, Tokyo Metropolitan Children’s Medical Center, Tokyo, 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)
  • Fukuzawa Ryuji ID: 9000345429607

    Department of Pathology and Laboratory Medicine, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan (2016 from CiNii)

    Articles in CiNii:1

    • A case of transient neonatal diabetes due to a novel mutation in <i>ABCC8</i> (2016)
  • Fukuzawa Ryuji ID: 9000391772502

    東京都立小児総合医療センター 検査科 (2011 from CiNii)

    Articles in CiNii:1

    • Ewing肉腫ファミリー腫瘍(ESFT)におけるHLA class I発現とCD8+Tリンパ球浸潤の検討 (2011)
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