Search Results1-20 of  22

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  • Ogawa Eishin ID: 9000394960692

    Articles in CiNii:1

    • A 2016 survey on adult height after growth hormone treatment in patients with idiopathic growth hormone deficiency : Combination treatment with anabolic steroid hormone improves adult height in boys (2018)
  • OGAWA EISHIN ID: 9000001617322

    Department of Pediatrics, School of Medicine (2004 from CiNii)

    Articles in CiNii:2

    • Refractory autoimmune hemolytic anemia in a patient with chromosome 22q11.2 deletion syndrome (2004)
    • Peripheral Blood Stem Cell Transplantation for Hepatoblastoma with Microscopical Residue : A Therapeutic Approach for Incompletely Resected Tumor (1998)
  • OGAWA EISHIN ID: 9000002099772

    Department of Pediatrics, Tohoku University School of Medicine (2006 from CiNii)

    Articles in CiNii:1

    • Kallmann Syndrome Phenotype in a Female Patient with CHARGE Syndrome and CHD7 Mutation (2006)
  • OGAWA EISHIN ID: 9000014156898

    Department of Pediatrics, Tohoku University Hospital (2008 from CiNii)

    Articles in CiNii:1

    • Hypospadias in a Male Patient with 21-hydroxylase Deficiency (2008)
  • OGAWA EISHIN ID: 9000253235107

    Department of Pediatrics, Tohoku University School of Medicine (1999 from CiNii)

    Articles in CiNii:1

    • Growth of Two Children after Six Months Interruption of GH Therapy (1999)
  • OGAWA Eishin ID: 9000000395205

    Articles in CiNii:26

    • A Case of Simple Virilizing Type of Steroid 21-Hydroxylase Deficiency Accompanied with Elevation of Deoxycorticosterone-Diagnosis by Gene Analysis Using Polymerase Chain Reaction- (1995)
    • An Infant of Oral-Facial-Digital Syndrome Associated with Precocious Puberty due to Hypothalamic Hamartoma. (1996)
    • Questionnairing about phenotypic difference of external genitalia in female sibrings with 21 hydroxylase deficiency in Japan. The Meeting of Active Pediatric Endocrinologists. (1997)
  • OGAWA Eishin ID: 9000257801786

    Department of Pediatrics, Tohoku University School of Medicine (2006 from CiNii)

    Articles in CiNii:1

    • Kallmann Syndrome Phenotype in a Female Patient with CHARGE Syndrome and CHD7 Mutation (2006)
  • OGAWA Eishin ID: 9000257803107

    Department of Pediatrics, Tohoku University Hospital (2008 from CiNii)

    Articles in CiNii:1

    • Hypospadias in a Male Patient with 21-hydroxylase Deficiency (2008)
  • OGAWA Eishin ID: 9000261667906

    Department of Pediatrics, Tohoku University Graduate School of Medicine, Tohoku University Graduate School of Pharmaceutical Sciences (2013 from CiNii)

    Articles in CiNii:1

    • Interaction of PICK1 with C-Terminus of Growth Hormone-Releasing Hormone Receptor (GHRHR) Modulates Trafficking and Signal Transduction of Human GHRHR (2013)
  • OGAWA Eishin ID: 9000261672910

    Department of Pediatrics, School of Medicine, Teikyo University (2013 from CiNii)

    Articles in CiNii:1

    • Combined linkage analysis and exome sequencing identifies novel genes for familial goiter (2013)
  • OGAWA Eishin ID: 9000283341050

    Department of Pediatrics, Teikyo University (2012 from CiNii)

    Articles in CiNii:1

    • Dietary education for children and lifestyle-related diseases in children (2012)
  • OGAWA Eishin ID: 9000348571424

    Department of Pediatrics, Tohoku University School of Medicine (2003 from CiNii)

    Articles in CiNii:7

    • Growth of Two Children after after Six Months Interruption of GH Therapy (1999)
    • Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiency (1999)
    • Novel mutation of L718X in the ATP7A gene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese population (2000)
  • OGAWA Eishin ID: 9000348576186

    Articles in CiNii:1

    • Mortality in patients with Congenital 21-Hydroxylase Deficiency Diagnosed after the Introduction of a Newborn Screening Program in Japan (2003)
  • Ogawa Eishin ID: 9000253167854

    Department of Pediatrics, School of Medicine (1991 from CiNii)

    Articles in CiNii:1

    • Effects of individual mutations in the P-450(C21) pseudogene on the P-450(C21) activity and their distribution in the patient genomes of congenital steroid 21-hydroxylase deficiency. (1991)
  • Ogawa Eishin ID: 9000255783993

    Department of Pediatircs Tohoku University School of Medicine (1993 from CiNii)

    Articles in CiNii:1

    • Genetic Analysis of Classical 21-Hydroxylase Deficiency Using Polymerase Chain Reaction and Allele-Specific Oligonucleotide Hybridization (1993)
  • Ogawa Eishin ID: 9000256286514

    Department of Pediatrics, Touhoku University School of Medicine (1992 from CiNii)

    Articles in CiNii:1

    • Phenotypic Variation in Patients with Partial Androgen Insensitivity Syndrome (1992)
  • Ogawa Eishin ID: 9000256287128

    Research Centre for Developmental Medicine and Biology, University of Auckland (1994 from CiNii)

    Articles in CiNii:1

    • Ovine Placental Lactogen (oPL) Lacks Anabolic Action in the Postnatal Lamb (1994)
  • Ogawa Eishin ID: 9000256287475

    Department of Pediatrics, Tohoku University School of Medicine (1996 from CiNii)

    Articles in CiNii:1

    • Effects of Pulsatile Gonadotropin Releasing Hormone and Human Chorionic Gonadotropin+Follice Stimulating Hormone Treatment on Pubertal Development in Two Cases with Panhypopituitarism (1996)
  • Ogawa Eishin ID: 9000257753664

    The Committee for the Newborn Screening of The Japanese Society for Pediatric Endocrinology (2003 from CiNii)

    Articles in CiNii:1

    • Mortality in Patients with Congenital 21-Hydroxylase Deficiency Diagnosed after the Introduction of a Newborn Screening Program in Japan (2003)
  • Ogawa Eishin ID: 9000257868106

    Department of Pediatrics, Tohoku University School of Medicine (1998 from CiNii)

    Articles in CiNii:1

    • Peripheral Blood Stem Cell Transplantation for Hepatoblastoma with Microscopical Residue: A Therapeutic Approach for Incompletely Resected Tumor. (1998)
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