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Department of Pediatrics, Hokkaido University School of Medicine | 論文
- Prognostic Factors in Childhood Acute Lymphoblastic Leukemia in Japan
- 3A3 IMPROVEMENT OF HEURISTIC METHOD FOR PRODUCTION PLANNING PROBLEM IN AUTO PARTS SUPPLIER(Technical session 3A : Sophisticated scheduling 1)
- A Japanese Patient of Congenital Hypothyroidism with Cerebellar Atrophy
- Total knee arthroplasty for rheumatoid knee with bilateral, severe flexion contracture : report of three cases
- Gender difference of slow wave sleep in middle aged and elderly subjects
- Evaluation of semantic processing in patients with temporal lobe epilepsy using event-related potential
- Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
- Elevated serum levels of soluble interleukin-2 receptor in juvenile dermatomyositis
- Impairment of myocardial flow reserve and endothelial function even in apparently normal coronary regions after Kawasaki disease using 15O-water PET
- Two Children with Xanthogranuloma of the Sellar Region
- Two Novel Mutations in the Thyroid Peroxidase Gene with Goitrous Hypothyroidism
- A Novel Heterozygous Mutation of Steroidogenic Factor-1 (SF-1/Ad4BP) Gene (NR5A1) in a 46, XY Disorders of Sex Development (DSD) Patient without Adrenal Failure
- Non-chromosome 15 marker chromosome in a Prader-Willi syndrome patient with uniparental disomy
- Inactivation of HDAC5 by SIK1 in AICAR-treated C2C12 Myoblasts
- Functional changes of the brainstem triggering vertex sharp wave with spindle
- A Forest Recreation Planning System Based on the Diversity of Recreation Experiences : The Meaning of the Recreation Opportunity Spectrum
- Support of Decision Making by Data Mining Using Neural System
- Development of Central Precocious Puberty After Surgical Resection in a Boy with Craniopharyngioma : Case Report
- Prolonged Bone Marrow Failure With Monosomy 7 After Engraftment Failure Following Bone Marrow Transplantation
- Gene Amplification as a Common Cause of lnherted Thyroxine-Binding Globulin Excess: Analysis of One Familial and Two Sporadic Cases