Search Results1-20 of  65

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  • FUKUSHIMA Yoshimitsu ID: 9000402493310

    Articles in CiNii:1

    • Visualization of the spatial positioning of the SNRPN, UBE3A, and GABRB3 genes in the normal human nucleus by three-color 3D fluorescence in situ hybridization (2012)
  • FUKUSHIMA YOSHIMITSU ID: 9000017693713

    Department of Medical Genetics, Shinshu University School of Medicine (2009 from CiNii)

    Articles in CiNii:1

    • Unusual Clinical and Pathological Presentation of a Neuroendocrine Tumor in a Patient with Multiple Endocrine Neoplasia Type 1 (2009)
  • FUKUSHIMA Yoshimitsu ID: 9000000093610

    Izumi Research Institute, Shimizu Corporation (1997 from CiNii)

    Articles in CiNii:1

    • Attenuation Characteristics of Peak Ground Motions in the 1995 Hyogo-ken Nanbu Earthquake (1997)
  • FUKUSHIMA Yoshimitsu ID: 9000000754376

    Articles in CiNii:14

    • Examination Concerning Dissociation of Left Ventricular Bolume Calculation Value Vased on Difference of Analytical Algorithm and Perfusion Tracer in Gated Myocardial SPECT (2001)
    • Assessment of Biventricular Function Using Gated Blood Pool SPECT with QBS Software : Comparison with Planar Radionuclide Ventriculography (2002)
    • 心筋SPECTと心臓CTを用いた Fusion 画像の臨床応用 (2008)
  • FUKUSHIMA Yoshimitsu ID: 9000001012967

    信州大学医学部附属病院遺伝子診療部 (2002 from CiNii)

    Articles in CiNii:2

    • Genetic testing and bioethics (2001)
    • 司会の言葉 (2002)
  • FUKUSHIMA Yoshimitsu ID: 9000001321384

    Division of Clinical and Molecular Genetics, Shinshu University Hospital (2004 from CiNii)

    Articles in CiNii:1

    • Comprehensive genetics clinic for familial tumors : proposal for a suitable system in Japan (2004)
  • FUKUSHIMA Yoshimitsu ID: 9000001331063

    Department of Hygiene, Shinshu University School of Medicine (1999 from CiNii)

    Articles in CiNii:1

    • Sequelae of Sarin Toxicity at One and Three Years After Exposure in Matsumoto, Japan (1999)
  • FUKUSHIMA Yoshimitsu ID: 9000001511453

    Department of Hygiene and Medical Genetics, Shinshu University School of Medicine (2001 from CiNii)

    Articles in CiNii:1

    • Progressive Scoliosis in Cri-Du-Chat Syndrome Over a 20-Year Follow-Up Period : A Case Report (2001)
  • FUKUSHIMA Yoshimitsu ID: 9000001758586

    Department of Medical Genetics, Shinshu University School of Medicine (2006 from CiNii)

    Articles in CiNii:1

    • Molecular characterization of a novel translocation t(5 ; 14)(q21 ; q32) in a patient with congenital abnormalities (2006)
  • FUKUSHIMA Yoshimitsu ID: 9000001858976

    Department of Preventive Medicine, Shinshu University School of Medicine (2007 from CiNii)

    Articles in CiNii:1

    • A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12 (2007)
  • FUKUSHIMA Yoshimitsu ID: 9000002060665

    Department of Medical Genetics, Shinshu University School of Medicine (2006 from CiNii)

    Articles in CiNii:1

    • A novel splicing mutation of the ATRX gene in ATR-X syndrome (2006)
  • FUKUSHIMA Yoshimitsu ID: 9000003849838

    DAIKIN Industries, Ltd. (2003 from CiNii)

    Articles in CiNii:1

    • Comfort Level Evaluation of the Air Purifier with Relaxation Effect using the Artificial Supersonic Wave(60th Anniversary Memorial Hall in Musashino Women's University) : (2003)
  • FUKUSHIMA Yoshimitsu ID: 9000003881343

    Department of Radiology, Graduate School of Radiology, Nippon Medical School (2011 from CiNii)

    Articles in CiNii:10

    • Assessment of left ventricular function using solid-state gamma camera equipped with a highly-sensitive collimator (2003)
    • Assessment of contractile response to dobutamine stress by means of ECG-gated myocardial SPECT : Comparison with myocardial perfusion and fatty acid metabolism (2005)
    • Serial assessment of left ventricular performance at rest and during bicycle exercise by ECG-gated myocardial perfusion SPECT (2002)
  • FUKUSHIMA Yoshimitsu ID: 9000003987398

    埼玉県立小児医療センター遺伝科 (1995 from CiNii)

    Articles in CiNii:3

    • Genetic Linkage Analyses of Romano-Ward Syndrome(RWS) in 13 Japanese Families (1995)
    • 我が国における家族性QT延長症候群の連鎖解析 : 第58回日本循環器学会学術集会 (1994)
    • 我が国におけるRomano-Ward症候群の遺伝解析 : 口述発表 : 第57回日本循環器学会学術集会 (1993)
  • FUKUSHIMA Yoshimitsu ID: 9000004074098

    The Investigation and Research Group for Idiopathic Cardiomyopathy,The ministry of Health and Welfare (1993 from CiNii)

    Articles in CiNii:1

    • GENETIC ANALYSIS OF ROMANOWARD SYNDROME IN JAPAN (1993)
  • FUKUSHIMA Yoshimitsu ID: 9000004945284

    Articles in CiNii:3

    • The effect of Sound field containing the supersonic wave on the Psychophysiological condition (2003)
    • Development of the Air purifier with relaxation effect using the artificial supersonic wave (2002)
    • The effect of Sound field containing the supersonic wave on the Psychophysiological condition (2003)
  • FUKUSHIMA Yoshimitsu ID: 9000005922628

    Articles in CiNii:28

    • Study on attenuation characteristics of peak ground acceleration of the 1995 Hyogo-ken Nanbu earthquake using the Digital National Land Information (1998)
    • Survey of Recent Studies on Attenuation Relation of Strong Ground Motion (Empirical Prediction Relation) (1993)
    • The Shape and Seismic Characteristics of the Philippine Sea Plate around the Iyo-nada, Schikoku, Japan, Judging from the Hypocenter Distribution (2003)
  • FUKUSHIMA Yoshimitsu ID: 9000006303534

    Division of Clinical and Molecular Genetics, Shinsyu University Hospital (2007 from CiNii)

    Articles in CiNii:1

    • Genetic Aspects of the Vascular Type of Ehlers-Danlos Syndrome (vEDS, EDSIV) in Japan (2007)
  • FUKUSHIMA Yoshimitsu ID: 9000006338094

    Department of Medical Genetics, Shinshu University School of Medicine (2011 from CiNii)

    Articles in CiNii:17

    • Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis : Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies (1999)
    • Guidelines for genetic testing (2001)
    • A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet (2002)
  • FUKUSHIMA Yoshimitsu ID: 9000016146366

    Division of Medical Genetics, Saitama Children's Medical Center (1995 from CiNii)

    Articles in CiNii:2

    • A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation (1995)
    • A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation (1995)
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