Search Results41-60 of  60

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  • Nishimura Gen ID: 9000003932421

    Dept. of Radiology, National Cardiovascular Center (1983 from CiNii)

    Articles in CiNii:1

    • DIAGNOSTIC ACCURACY OF INTRAVENOUS DIGITAL SUBTRACTION ANGIOGRAPHY (IVDSA) IN THE EVALUATION OF PATENCY OF AC-BYPASS : PROCEEDINGS OF THE 47th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY : Ischemic Heart Disease (II) (1983)
  • Nishimura Gen ID: 9000238888405

    Articles in CiNii:3

    • Intra-arterial Digital Subtraction Angiography (IA-DSA) with Cardon Dioxide (1988)
    • Left Ventricular Volmetry in Long-axial and Conventional Projection (1982)
    • Intra-Arterial Digital Subtraction Angiography with Carbon Dioxide (1987)
  • Nishimura Gen ID: 9000239585634

    Articles in CiNii:1

    • Prenatal diagnosis of short-rib polydactyly syndrome type 3 (Verma-Naumoff type) by three-dimensional helical computed tomography (2011)
  • Nishimura Gen ID: 9000256286633

    Departments of Pediatrics and Diagnostic Radiology, Keio University School of Medicine (1993 from CiNii)

    Articles in CiNii:1

    • A New Overgrowth Syndrome with Megaepiphysis and Hypertrophy of the Mitral Valve (1993)
  • Nishimura Gen ID: 9000256286759

    Department of Radiology, Shimizu City Hospital (1994 from CiNii)

    Articles in CiNii:1

    • New Congenital Malformation Syndrome with Severe Short Stature, Craniosynostosis, and Generalized Osseous Dysplasia in Two Siblings; New Osseous Dysplasia in Two Siblings (1994)
  • Nishimura Gen ID: 9000256287810

    Department of Radiology, Dokkyo University School of Medicine (1997 from CiNii)

    Articles in CiNii:1

    • Practical Approach to Radiologic Diagnosis of Bone Dysplasias: Bone Dysplasia Family (1997)
  • Nishimura Gen ID: 9000257753548

    Department of Radiology, Nasu Central Hospital (2001 from CiNii)

    Articles in CiNii:1

    • Auxological and Radiological Manifestations of Patients with Hypochondroplasia Negative for N540K Mutation in Fibroblast Growth Factor Receptor 3 Gene. (2001)
  • Nishimura Gen ID: 9000298897525

    Department of Radiology, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan (2015 from CiNii)

    Articles in CiNii:1

    • A case of spondyloepiphyseal dysplasia tarda caused by a novel intragenic deletion of <i>TRAPPC2</i> (2015)
  • Nishimura Gen ID: 9000329014114

    Department of Radiology, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan (2016 from CiNii)

    Articles in CiNii:1

    • A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in <i>COL10A1</i> (2016)
  • Nishimura Gen ID: 9000329014144

    Department of Radiology, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan (2016 from CiNii)

    Articles in CiNii:1

    • A Japanese familial case of hypochondroplasia with a novel mutation in <i>FGFR3</i> (2016)
  • Nishimura Gen ID: 9000362203196

    Articles in CiNii:1

    • A Case with Spondyloenchondrodysplasia Treated with Growth Hormone (2017)
  • Nishimura Gen ID: 9000387904301

    Intractable Disease Center, Saitama Medical University Hospital (2017 from CiNii)

    Articles in CiNii:1

    • Bone dysplasia families (2017)
  • Nishimura Gen ID: 9000397684659

    Center for Intractable Diseases, Saitama Medical University Hospital, Saitama, Japan (2018 from CiNii)

    Articles in CiNii:1

    • A familial case of spondyloepiphyseal dysplasia tarda caused by a novel splice site mutation in <i>TRAPPC2</i> (2018)
  • Nishimura Gen ID: 9000398156008

    Articles in CiNii:1

    • Platyspondylic lethal dysplasia torrance type with a heterozygous mutation in the triple helical domain of COL2A1 in two sibs from phenotypically normal parents. (2012)
  • Nishimura Gen ID: 9000401559150

    Department of Pediatric Imaging; Tokyo Metropolitan Children's Medical Center; Fuchu-shi Tokyo Japan (2013 from CiNii)

    Articles in CiNii:1

    • Prenatal diagnosis of cervical spinal cord compression in chondrodysplasia punctata brachytelephalangic type: A case report and literature review:Prenatal cervical compression in CDP-B (2013)
  • Nishimura Gen ID: 9000401560224

    Department of Pediatric Imaging; Tokyo Metropolitan Children's Medical Center; Tokyo Japan (2017 from CiNii)

    Articles in CiNii:1

    • Progressive subglottic stenosis in a child with Pallister-Killian syndrome:Subglottic stenosis in PKS (2017)
  • Nishimura Gen ID: 9000401560408

    Intractable Disease Center; Saitama Medical University Hospital; Saitama Japan (2018 from CiNii)

    Articles in CiNii:1

    • Familial campomelic dysplasia due to maternal germinal mosaicism:Familial campomelic dysplasia (2018)
  • Nishimura Gen ID: 9000401563582

    Articles in CiNii:1

    • Prenatal diagnosis of osteogenesis imperfecta type II by three-dimensional computed tomography: The current state of fetal computed tomography:Prenatal diagnosis of OI type II (2012)
  • Nishimura Gen ID: 9000402093763

    Articles in CiNii:1

    • Identification of a homozygous frameshift variant in RFLNA in a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome (2019)
  • Nishimura Gen ID: 9000404481295

    Articles in CiNii:1

    • National survey of prevalence and prognosis of thanatophoric dysplasia in Japan (2019)
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