Search Results1-20 of  67

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  • Okamoto Nobuhiko ID: 9000242145715

    Articles in CiNii:1

    • Novel FIG4 mutations in Yunis-Varon syndrome (2013)
  • Okamoto Nobuhiko ID: 9000271154432

    Articles in CiNii:1

    • KIF1A mutation in a patient with progressive neurodegeneration (2014)
  • Okamoto Nobuhiko ID: 9000314400488

    Articles in CiNii:1

    • Gastric tube cancer after radical esophagectomy : comparison of two periods in a single center (2016)
  • Okamoto Nobuhiko ID: 9000322731238

    Articles in CiNii:1

    • SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements (2016)
  • Okamoto Nobuhiko ID: 9000324662902

    Articles in CiNii:1

    • De novo KCNH1 mutations in four patients with syndromic developmental delay, hypotonia and seizures (2016)
  • Okamoto Nobuhiko ID: 9000324663234

    Articles in CiNii:1

    • De novo missense mutations in NALCN cause developmental and intellectual impairment with hypotonia (2016)
  • Okamoto Nobuhiko ID: 9000333078491

    Articles in CiNii:1

    • De novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux (2016)
  • OKAMOTO NOBUHIKO ID: 9000001683900

    Osaka Medical Center and Research Institute for Maternal and Child Health, Planning and Research (2005 from CiNii)

    Articles in CiNii:1

    • Malignant retroperitoneal tumor arising in a multicystic dysplastic kidney of a girl with Schinzel-Giedion syndrome (2005)
  • OKAMOTO Nobuhiko ID: 9000000437449

    Department of planning and Research,Osaka Medical Center and Research Instiute for Maternal and Child Health (1997 from CiNii)

    Articles in CiNii:1

    • L1CAM mutation in a Japanese family with x-linked hydrocephalus: a study for genetic counseling (1997)
  • OKAMOTO Nobuhiko ID: 9000001076660

    Department of Molecular Cytogenetics, Medical Research Institute and School of Biomedical Science, Tokyo Medical and Dental University (2012 from CiNii)

    Articles in CiNii:14

    • A clinical and molecular study of a patient with Simpson-Golabi-Behmel syndrome (1999)
    • A 1-Mb critical region in six patients with 9q34.3 terminal deletion syndrome (2004)
    • Chromosome 1q deletion and congenital glaucoma (2005)
  • OKAMOTO Nobuhiko ID: 9000001260301

    Department of Planning and Research, Osaka Medical Center and Research Institute for Maternal and Child Health (2004 from CiNii)

    Articles in CiNii:1

    • Hydrocephalus and Hirschsprung's disease with a mutation of L1CAM (2004)
  • OKAMOTO Nobuhiko ID: 9000001361783

    Department of Planning and Research, Osaka Medical Center and Research Institute for Maternal and Child Health (1995 from CiNii)

    Articles in CiNii:1

    • A PATIENT WITH SCHINZEL-GIEDION SYNDROME AND A REVIEW OF 20 PATIENTS (1995)
  • OKAMOTO Nobuhiko ID: 9000001362456

    Department of Planning and Research, Osaka Medical Center and Research Institute for Maternal and Child Health (1996 from CiNii)

    Articles in CiNii:1

    • A NOVEL MUTATION IN L1CAM GENE IN A JAPANESE PATIENT WITH X-LINKED HYDROCEPHALUS (1996)
  • OKAMOTO Nobuhiko ID: 9000001362820

    Department of Planning and Research, Osaka Medical Center and Research Institute for Maternal and Child Health (1997 from CiNii)

    Articles in CiNii:1

    • MEVALONIC ACIDEMIA : FIRST CASE OF JAPAN (1997)
  • OKAMOTO Nobuhiko ID: 9000002889350

    Department of Surgery, School of Medicine, Keiko University (2004 from CiNii)

    Articles in CiNii:22

    • 食道癌根治術における術前ステロイド投与の周術期病態に及ぼす影響 : 二重盲検法による比較 (2001)
    • OP-3-025 頭頚部癌患者の上部消化管内視鏡スクリーニング検査による食道癌の検出と治療法の検討 (2002)
    • PP-1-398 食道癌のセンチネルリンパ節を指標とした転移診断の有用性と問題点 (2002)
  • OKAMOTO Nobuhiko ID: 9000002948625

    さいたま市立病院外科 (2014 from CiNii)

    Articles in CiNii:27

    • A CASE CECUM CARCINOMA WITH INTERNAL COLONIC FISTULA PRESENTED WITH A PELVIC TUMOR (2006)
    • A CASE OF SIGMOIDCUTANEOUS FISTULA DUE TO DIVERTICULITIS (2007)
    • A CASE OF ADENOSQUAMOUS CARCINOMA OF THE PANCREAS FOUND WITH ELEVATED SERUM CEA VALUE (2008)
  • OKAMOTO Nobuhiko ID: 9000004392753

    Department of Pediatrics, Shiga University of Medical Science (2005 from CiNii)

    Articles in CiNii:4

    • Morphological differences in cardiovascular anomalies induced by bis-diamine between Sprague-Dawley and Wistar rats (2005)
    • Teratogenic effect of bis-diamine on embryonic rat heart (2000)
    • Diaphragmatic Hernia Induced in Rat Fetuses by Administration of Bisdiamine (1992)
  • OKAMOTO Nobuhiko ID: 9000018778762

    Developmental Pediatrics, Osaka Medical Center and Research Institute for Maternal and Child Health (2010 from CiNii)

    Articles in CiNii:1

    • Brachmann-de Lange syndrome with congenital diaphragmatic hernia and NIPBL gene mutation (2010)
  • OKAMOTO Nobuhiko ID: 9000019147083

    Osaka Medical Center and Research Institute for Maternal and Child health, Medicat Genetics (2011 from CiNii)

    Articles in CiNii:1

    • Commentary on 'Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome' (2011)
  • OKAMOTO Nobuhiko ID: 9000019187493

    Department of Planning and Research, Osaka Medical Center and Research Institute for Maternal and Child Health (2009 from CiNii)

    Articles in CiNii:1

    • Mucolipidosis II and III alpha/beta : mutation analysis of 40 Japanese patients showed genotype-phenotype correlation (2009)
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