Search Results1-20 of  46

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  • SEKIJIMA Yoshiki ID: 9000000562596

    the Department of Neurology, the Department of Medicine (Neurology), Shinshu University School of Medicine (2001 from CiNii)

    Articles in CiNii:1

    • Three Patients with Isolated Adrenocorticotropin Deficiency Presenting with Neuroleptic Malignant Syndrome-like Symptoms (2001)
  • SEKIJIMA Yoshiki ID: 9000000743078

    Third Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine (2011 from CiNii)

    Articles in CiNii:16

    • Cytoplasmic Body Myopathy with Hypertrophic Cardiomyopathy (1995)
    • Malignant Lymphoma Associated with Rheumatoid Arthritis, Developing Shortly after Initiation of Oral Methotrexate (2004)
    • A Novel RNA Splice Site Mutation in the C1 Inhibitor Gene of a Patient with Type I Hereditary Angioedema (2004)
  • SEKIJIMA Yoshiki ID: 9000001182528

    Third Department of Medicine, Shinshu University School of Medicine (2003 from CiNii)

    Articles in CiNii:1

    • Hepatocellular Carcinoma in a Case of Adult-onset Type II Citrullinemia (2003)
  • SEKIJIMA Yoshiki ID: 9000006577355

    Articles in CiNii:20

    • A case of severe sarin poisoning in the Sarin Attack in Matsumoto : One-year follow-up of clinical findings, and laboratory data (1995)
    • A case of chronic inflammatory demyelinating polyradiculoneuropathy complicated by phrenic nerve palsy (1998)
    • A case of severe status epilepticus of frontal lobe origin successfully treated with corticosteroids (1998)
  • SEKIJIMA Yoshiki ID: 9000019188289

    Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine (2010 from CiNii)

    Articles in CiNii:1

    • Cerebral hemorrhage in Fabry's disease (2010)
  • SEKIJIMA Yoshiki ID: 9000258246483

    Division of Clinical and Molecular Genetics, Department of Neurology and Rheumatology, Shinshu University Hospital (2008 from CiNii)

    Articles in CiNii:1

    • Pathogenesis and Therapeutic Strategy for Protein Misfolding Disease (2008)
  • SEKIJIMA Yoshiki ID: 9000258246980

    信州大学医学部内科学第三講座 (2014 from CiNii)

    Articles in CiNii:1

    • 家族性アミロイドポリニューロパチーに対する新規治療―神経変性疾患治療の新たな時代の幕開け― (2014)
  • SEKIJIMA Yoshiki ID: 9000263059945

    Division of Clinical and Molecular Genetics, Shinshu University School of Medicine (2013 from CiNii)

    Articles in CiNii:1

    • Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan (2013)
  • SEKIJIMA Yoshiki ID: 9000319550694

    Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine|Department of Biological Sciences for Intractable Neurological Disorders, Institute for Biomedical Sciences, Shinshu University (2016 from CiNii)

    Articles in CiNii:1

    • Recurrence of Waldenström macroglobulinemia accompanied by factor X deficiency (2016)
  • SEKIJIMA Yoshiki ID: 9000402071887

    Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine (2019 from CiNii)

    Articles in CiNii:1

    • Quantitative Analysis of Endocardial and Epicardial Left Ventricular Myocardial Deformation in Patients with Cardiac Amyloidosis (2019)
  • SEKIJIMA Yoshiki ID: 9000402771825

    信州大学医学部内科学第三教室 (2019 from CiNii)

    Articles in CiNii:1

    • Aging and Amyloidosis (2019)
  • Sekijima Yoshiki ID: 9000022068699

    Division of Clinical and Molecular Genetics, Shinshu University Hospital, Japan (2012 from CiNii)

    Articles in CiNii:1

    • Two Siblings Diagnosed to Have Transthyretin-related Familial Amyloid Cardiomyopathy Around the Same Time at Different Hospitals (2012)
  • Sekijima Yoshiki ID: 9000237886642

    Articles in CiNii:1

    • Successful Pregnancy and Lactation Outcome in a Patient With Gaucher Disease Receiving Enzyme Replacement Therapy, and the Subsequent Distribution and Excretion of Imiglucerase in Human Breast Milk (2010)
  • Sekijima Yoshiki ID: 9000237886785

    Articles in CiNii:1

    • High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly (2011)
  • Sekijima Yoshiki ID: 9000237886821

    Articles in CiNii:1

    • CPPD crystal deposition disease of the cervical spine: A common cause of acute neck pain encountered in the neurology department (2010)
  • Sekijima Yoshiki ID: 9000237886863

    Articles in CiNii:1

    • A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea (2012)
  • Sekijima Yoshiki ID: 9000240055630

    Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Japan|Division of Clinical and Molecular Genetics, Shinshu University Hospital, Japan (2013 from CiNii)

    Articles in CiNii:1

    • Clinical and Serial MRI Findings of a Sialidosis Type I Patient with a Novel Missense Mutation in the <i>NEU1</i> Gene (2013)
  • Sekijima Yoshiki ID: 9000242352414

    Articles in CiNii:1

    • Marked intrafamilial phenotypic variation in a family with SOD1 C111Y mutation (2012)
  • Sekijima Yoshiki ID: 9000250186409

    Articles in CiNii:1

    • Clinical and Serial MRI Findings of a Sialidosis Type I Patient with a Novel Missense Mutation in the NEU1 Gene (2013)
  • Sekijima Yoshiki ID: 9000258058675

    Division of Clinical and Molecular Genetics, Shinshu University Hospital (2010 from CiNii)

    Articles in CiNii:1

    • Familial Amyloid Polyneuropathy: Diflunisal (2010)
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