Search Results1-20 of  84

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  • Miyake Noriko ID: 9000402821619

    Department of Human Genetics, Yokohama City University Graduate School of Medicine, Japan (2019 from CiNii)

    Articles in CiNii:1

    • Novel <i>VRK1</i> Mutations in a Patient with Childhood-onset Motor Neuron Disease (2019)
  • Miyake Noriko ID: 9000404155747

    Articles in CiNii:1

    • Measurement of Serum Tenascin-X in Joint Hypermobility Syndrome Patients (2019)
  • Miyake Noriko ID: 9000324662905

    Articles in CiNii:1

    • De novo KCNH1 mutations in four patients with syndromic developmental delay, hypotonia and seizures (2016)
  • Miyake Noriko ID: 9000324663246

    Articles in CiNii:1

    • De novo missense mutations in NALCN cause developmental and intellectual impairment with hypotonia (2016)
  • Miyake Noriko ID: 9000326637979

    Articles in CiNii:1

    • Milder progressive cerebellar atrophy caused by biallelic SEPSECS mutations (2016)
  • Miyake Noriko ID: 9000326638156

    Articles in CiNii:1

    • Human genetic variation database, a reference database of genetic variations in the Japanese population (2016)
  • Miyake Noriko ID: 9000329423401

    Articles in CiNii:1

    • WDR45 mutations in three male patients with West syndrome (2016)
  • Miyake Noriko ID: 9000333078495

    Articles in CiNii:1

    • De novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux (2016)
  • Miyake Noriko ID: 9000333078508

    Articles in CiNii:1

    • Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinism (2016)
  • Miyake Noriko ID: 9000345445654

    Articles in CiNii:1

    • Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia (2017)
  • Miyake Noriko ID: 9000345445700

    Articles in CiNii:1

    • Novel and recurrent XYLT1 mutations in two Turkish families with Desbuquois dysplasia, type 2 (2017)
  • Miyake Noriko ID: 9000356596923

    Articles in CiNii:1

    • Axial spondylometaphyseal dysplasia is also caused by NEK1 mutations (2017)
  • Miyake Noriko ID: 9000356876351

    Articles in CiNii:1

    • PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder (2017)
  • Miyake Noriko ID: 9000356876573

    Articles in CiNii:1

    • Novel KCNB1 mutation associated with non-syndromic intellectual disability (2017)
  • AE Mieko ENDO Toshio MIYAKE Noriko ID: 9000006926888

    Articles in CiNii:2

    • Title: Research reviews about social identity in sports (1985-2008 English limited) (2009)
    • Report on Psychological Supports for a Japan National Female Team (2012)
  • MIYAKE NORIKO ID: 9000019064121

    Department of Clinical Immunology and Rheumatology/Infectious Diseases, Kyushu University Hospital (2011 from CiNii)

    Articles in CiNii:1

    • Successful combination therapy with vancomycin and arbekacin against infective endocarditis caused by MRSA (2011)
  • MIYAKE NORIKO ID: 9000020730152

    Articles in CiNii:1

    • A STUDY OF PHYSIQUE AND PHYSICAL FITNESS OF FIELD HOCKEY PLAYERS (II):—A CASE OF JAPANESE NATIONAL WOMEN'S FIELD HOCKEY PLAYERS— (1988)
  • MIYAKE NORIKO ID: 9000020735290

    Articles in CiNii:1

    • A STUDY OF PHYSIQUE AND PHYSICAL FITNESS OF FIELD HOCKEY PLAYERS (I):—A CASE OF JAPANESE NATIONAL MEN'S FIELD HOCKEY PLAYERS— (1986)
  • MIYAKE NORIKO ID: 9000256789293

    Department of Clinical and Research Laboratory, JR Tokyo General Hospital (1990 from CiNii)

    Articles in CiNii:1

    • ANTIBACTERIAL ACTIVITY OF IMIPENEM IN COMBINATION WITH AMPICILLIN AGAINST METHICILLIN-RESISTANT STRAINS OF <I>STAPHYLOCOCCUS AUREUS</I> (1990)
  • MIYAKE NORIKO ID: 9000256802139

    Departments of Clinical Pathology (2007 from CiNii)

    Articles in CiNii:1

    • IN VITRO ACTIVITY OF CEFOTIAM AGAINST OXACILLINRESISTANT <I>Staphylococcus epidermidis</I> STRAINS:REEVALUATION OF BETA-LACTAM EFFICIENCY ON MRSE (2007)
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