Search Results1-20 of  23

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  • Asakura Yumi ID: 9000329423177

    Articles in CiNii:1

    • Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri–Weill dyschondrosteosis (2016)
  • ASAKURA YUMI ID: 9000020660864

    Department of Pediatrics, Nippon Medical School First Hospital (1991 from CiNii)

    Articles in CiNii:1

    • Application of Improved Coupling Assay Method for Peroxidase of Diseased Thyroids: Report of Three Cases. (1991)
  • ASAKURA YUMI ID: 9000252824884

    Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center (1999 from CiNii)

    Articles in CiNii:1

    • A Male Patient Presenting with Major Clinical Symptoms of Glucocorticoid Deficiency and Skeletal Dysplasia, showing a Steroid Pattern Compatible with 17.ALPHA.-Hydroxylase/ 17, 20-Lyase Deficiency, but without Obvious CYP 17 Gene Mutations. (1999)
  • ASAKURA YUMI ID: 9000348582306

    Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center (2010 from CiNii)

    Articles in CiNii:3

    • Novel SLC12A1 (NKCC2) Mutations in Two Families with Bartter Syndrome Type 1 (2007)
    • Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism (2010)
    • Prevalence of Obesity, Hyperlipemia and Insulin Resistance in Children with Suprasellar Brain Tumors (2007)
  • ASAKURA Yumi ID: 9000000384531

    Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center (2004 from CiNii)

    Articles in CiNii:3

    • A Male Patient Presenting with Major Clinical Symptoms of Glucocorticoid Deficiency and Skeletal Dysplasia, showing a Steroid Pattern Compatible with 17α-Hydroxylase/17m,20-Lyase Deficiency, but without Obvious CYP17 Gene Mutations (1999)
    • Abnormal steroidogenesis in three patients with Antley-Bixler syndrome : Apparent decreased activity of 17α-hydroxylase, 17,20-lyase and 21-hydroxylase (2004)
    • Bone Mineral Density and Bone Metabolic Markers in Children with Hyperthyroidism Before and During Treatment (2000)
  • ASAKURA Yumi ID: 9000000395830

    The Department of Pediatrics, Nippon Mediacl School (1998 from CiNii)

    Articles in CiNii:1

    • Study of Body Fat Ratio, Subcutaneous Fat Thickness and Metabolic parameters in Obese Children (1998)
  • ASAKURA Yumi ID: 9000000485522

    Articles in CiNii:30

    • Eight Cases of Central Hypothyroidism Detected by Mass-screening for Congenital Hypothyroidism Using Simultaneous Measurement of TSH and T4 or ft4 (2000)
    • Long-Term Prognosis of Central Precocious Puberty. (1998)
    • ターナー症候群 [del(X) (p 11.4)] の母娘例 (2000)
  • ASAKURA Yumi ID: 9000257802302

    Department of Endocrinology & Metabolism, Clinical Research Institute, Kanagawa Children's Medical Center (2007 from CiNii)

    Articles in CiNii:1

    • Novel SLC12A1 (NKCC2) Mutations in Two Families with Bartter Syndrome Type 1 (2007)
  • ASAKURA Yumi ID: 9000265572011

    Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center (2013 from CiNii)

    Articles in CiNii:1

    • Association Between Graves' Disease and Renal Coloboma Syndrome : A Case Report (2013)
  • Asakura Yumi ID: 9000256286582

    Department of Endocrinology and Metabolism Kanagawa Children's Medical Center (1993 from CiNii)

    Articles in CiNii:1

    • Incomplete Growth Hormone Secretion with Pituitary Stalk Transection and Syringomyelia (1993)
  • Asakura Yumi ID: 9000256286729

    Department of pediatrics, Kanagawa Children's Medical Center (1994 from CiNii)

    Articles in CiNii:1

    • Resumption of Puberty in Girls and Boys with Central Precocious Puberty After Withdrawal of Long-Term Therapy with LHRH-Analogue D-Ser-6-LHRH (1994)
  • Asakura Yumi ID: 9000256286761

    Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center (1994 from CiNii)

    Articles in CiNii:1

    • New Congenital Malformation Syndrome with Severe Short Stature, Craniosynostosis, and Generalized Osseous Dysplasia in Two Siblings; New Osseous Dysplasia in Two Siblings (1994)
  • Asakura Yumi ID: 9000257754064

    Department of Endocrinology and Metabolism, Clinical Research Institute, Kanagawa Children's Medical Center (2007 from CiNii)

    Articles in CiNii:1

    • Prevalence of Obesity, Hyperlipemia and Insulin Resistance in Children with Suprasellar Brain Tumors (2007)
  • Asakura Yumi ID: 9000257754441

    Department of Endocrinology and Metabolism, Kanagawa Children’s Medical Center, Kanagawa, Japan (2014 from CiNii)

    Articles in CiNii:1

    • Therapeutic Use of Oral Sodium Phosphate (Phosribbon<sup>®</sup> Combination Granules) in Hereditary Hypophosphatemic Rickets (2014)
  • Asakura Yumi ID: 9000257754550

    Department of Pediatrics, Kanagawa Children’s Medical Center, Yokohama, Japan (1999 from CiNii)

    Articles in CiNii:1

    • Consecutive Urinary Gonadotropin and Ovarian Hormone Excretory Patterns during LH-RH Analog Treatment in Female Patients with Central Precocious Puberty (1999)
  • Asakura Yumi ID: 9000257754576

    Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center (2000 from CiNii)

    Articles in CiNii:1

    • Bone Mineral Density and Bone Metabolic Markers in Children with Hyperthyroidism Before and During Treatment (2000)
  • Asakura Yumi ID: 9000259833325

    Department of Endocrinology and Metabolism, Kanagawa Children’s Medical Center, Yokohama 232-8555, Japan (2014 from CiNii)

    Articles in CiNii:1

    • Overall usefulness of newborn screening for congenital hypothyroidism by using free thyroxine measurement (2014)
  • Asakura Yumi ID: 9000283362865

    Department of Endocrinology and Metabolism, Kanagawa Children’s Medical Center, Yokohama, Japan (2013 from CiNii)

    Articles in CiNii:1

    • Abnormal Adipose Tissue Distribution with Unfavorable Metabolic Profile in Five Children Following Hematopoietic Stem Cell Transplantation: A New Etiology for Acquired Partial Lipodystrophy (2013)
  • Asakura Yumi ID: 9000283362942

    Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan (2015 from CiNii)

    Articles in CiNii:1

    • Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous <i>PROKR2</i> mutation (2015)
  • Asakura Yumi ID: 9000329014161

    Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan (2016 from CiNii)

    Articles in CiNii:1

    • Potential utility of cinacalcet as a treatment for <i>CDC73</i>-related primary hyperparathyroidism: a case report (2016)
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