Search Results1-20 of  28

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  • Ihara Kenji ID: 9000324663241

    Articles in CiNii:1

    • De novo missense mutations in NALCN cause developmental and intellectual impairment with hypotonia (2016)
  • IHARA KENJI ID: 9000018772275

    Department of Applied Chemistry, Faculty of Engineering, Kansai University (1995 from CiNii)

    Articles in CiNii:1

    • PREPARATION OF CHITOSAN AND MANNAN DERIVATIVES HAVING CARBOXYLIC ACID GROUPS BY PERIODATE OXIDATION AND THEIR FUNCTION (1995)
  • IHARA KENJI ID: 9000107354781

    Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2004 from CiNii)

    Articles in CiNii:1

    • Association Study of Human MTH1 Gene Polymorphisms with Type 1 Diabetes Mellitus (2004)
  • IHARA Kenji ID: 9000000191301

    九大・医・小児 (1998 from CiNii)

    Articles in CiNii:1

    • Cloning of gene encoding human methylcrotonyl CoA carboxylase(MCC) (1998)
  • IHARA Kenji ID: 9000001269399

    Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2009 from CiNii)

    Articles in CiNii:5

    • Acid maltase 遺伝子新規ナンセンス変異とアミノグリコシド系抗生物質の読み飛ばし効果の検討 (2001)
    • TPO受容体 (c-mpl) 異常と先天性無巨核球性血小板減少症 (2005)
    • Genetic background of congenital thrombocytopenia (2008)
  • IHARA Kenji ID: 9000001380231

    Graduate School of Science, Himeji Institute of Technology (2003 from CiNii)

    Articles in CiNii:1

    • Generation of Cycloheptyne during the Solvolysis of Cyclohexylidenemethyliodonium Salt in the Presence of Base (2003)
  • IHARA Kenji ID: 9000002036190

    Department of Pediatrics, Graduate School of Medicine, Kyushu University (2010 from CiNii)

    Articles in CiNii:2

    • Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency (2007)
    • Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations (2010)
  • IHARA Kenji ID: 9000003459489

    Division of Neonatology, Comprehensive Maternity and Perinatal Care Center, Kyushu University (2011 from CiNii)

    Articles in CiNii:16

    • Identification of mutations in thrombopoietin receptor gene(c-mpl)in congential amegakaryocytic thrombocytopenia (1998)
    • 先天性補体欠損症: その臨床的特微と遺伝子異常 (1999)
    • Thrombocytopenia and c-mpl Gene Mutation (2002)
  • IHARA Kenji ID: 9000005066496

    大阪大学大学院 工学研究科:(現)川崎製鉄 (1999 from CiNii)

    Articles in CiNii:6

    • Microstructures and Mechanical Properties of Laser Welds of High Strength Steel Sheet (1997)
    • Quantitative formulation of hardness for heat affected zones in laser welds (1998)
    • Effects of shielding Gas on Mechanical Properties of laser welds of Ti Contents steels (1998)
  • IHARA Kenji ID: 9000011255660

    Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2003 from CiNii)

    Articles in CiNii:4

    • A Case of Growth Hormone and Gonadotropin Deficiency Associated with Unilateral Anophthalmia, Microphallus, Cryptorchidism, and Mental Retardation (2002)
    • Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in Japan (1999)
    • Novel polymorphism in the 5'-untranslated region of the interleukin-4 gene (1999)
  • IHARA Kenji ID: 9000019147880

    Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2011 from CiNii)

    Articles in CiNii:1

    • HRAS mutants identified in Costello syndrome patients can induce cellular senescence : possible implications for the pathogenesis of Costello syndrome (2011)
  • IHARA Kenji ID: 9000256642484

    Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2000 from CiNii)

    Articles in CiNii:1

    • An Infant with Hurler Syndrome. Successful Engraftment after Unrelated Cord Blood Transplantation. (2000)
  • IHARA Kenji ID: 9000256643080

    Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2002 from CiNii)

    Articles in CiNii:1

    • Thrombocytopenia and c-mpl Gene Mutation. (2002)
  • IHARA Kenji ID: 9000257800878

    Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2004 from CiNii)

    Articles in CiNii:1

    • Association Study of Human MTH1 Gene Polymorphisms with Type 1 Diabetes Mellitus (2004)
  • IHARA Kenji ID: 9000263059959

    Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2013 from CiNii)

    Articles in CiNii:1

    • Newborn screening for Fabry disease in Japan : prevalence and genotypes of Fabry disease in a pilot study (2013)
  • IHARA Kenji ID: 9000265572484

    Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2008 from CiNii)

    Articles in CiNii:1

    • Case Report : Adjuvant Therapy with a High Dose of Mitotane for Adrenocortical Carcinoma in a 4-year-old Boy (2008)
  • Ihara Kenji ID: 9000256023055

    Graduate School of Science, Himeji Institute of Technology (2003 from CiNii)

    Articles in CiNii:1

    • Generation of Cycloheptyne during the Solvolysis of Cyclohexylidenemethyliodonium Salt in the Presence of Base (2003)
  • Ihara Kenji ID: 9000283362908

    Department of Pediatrics, Graduate School of Medical Science, Kyushu University, Fukuoka, Japan (2014 from CiNii)

    Articles in CiNii:1

    • Thyroid Follicular Carcinoma in a Fourteen-year-old Girl with Graves' Disease (2014)
  • Ihara Kenji ID: 9000283741636

    Himeji Inst. of Tech. (2003 from CiNii)

    Articles in CiNii:1

    • Cycloheptyne Formation from Cyclohexylidenemethyliodonium Salt in Fluoro Alcohols (2003)
  • Ihara Kenji ID: 9000345301095

    Departments of Pediatrics, Graduate School of Medical Sciences, Kyushu University (2016 from CiNii)

    Articles in CiNii:1

    • Analysis of Death Due to Infectious Diseases in Patients Hospitalized in the Pediatric Ward of a Single Japanese Tertiary Medical Facility (2016)
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