Showing 21 - 40 results of 65 for search 'Han Wook Yoo', query time: 0.14s Refine Results
  1. 21
    A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by an unpublished mutation of
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  2. 22
    Two cases of Fabry disease identified in brothers
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  3. 23
    Long-term clinical course of a patient with mucopolysaccharidosis type IIIB
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  4. 24
    Case report of unexpected gastrointestinal involvement in type 1 Gaucher disease: comparison of eliglustat tartrate treatment and enzyme replacement therapy
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  5. 25
    Etiologic distribution and clinical characteristics of pediatric diabetes in 276 children and adolescents with diabetes at a single academic center
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  6. 26
    Long-term follow-up on Cushing disease patient after transsphenoidal surgery
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  7. 27
    Two cases of chronic pancreatitis associated with anomalous pancreaticobiliary ductal union and mutation
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  8. 28
    Diabetes mellitus caused by secondary hemochromatosis after multiple blood transfusions in 2 patients with severe aplastic anemia
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  9. 29
    Long-term clinical outcome and the identification of homozygous gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1A
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  10. 30
    Mutation Spectrum of STAR and the Founder Effect of p.Q258* in Korean Patients with Congenital Lipoid Adrenal Hyperplasia
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  11. 31
    Predominance of the c.648G > T G6PC gene mutation and late complications in Korean patients with glycogen storage disease type Ia
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  12. 32
    Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial
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  13. 33
    A novel mutation within gene in a young girl with hypophosphatemic rickets and review of literature
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  14. 34
    The natural history and prognostic factors of Graves' disease in Korean children and adolescents
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  15. 35
    Endocrine dysfunction after bone marrow transplantation during childhood and adolescence
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  16. 36
    Chronic intermittent form of isovaleric aciduria in a 2-year-old boy
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  17. 37
    Two cases of familial cerebral cavernous malformation caused by mutations in the gene
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  18. 38
    A case of an infant suspected as IMAGE syndrome who were finally diagnosed with MIRAGE syndrome by targeted Mendelian exome sequencing
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  19. 39
    Long-term efficacy of recombinant human growth hormone therapy in short-statured patients with Noonan syndrome
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  20. 40
    Magnetic resonance imaging and spectroscopic analysis in 5 cases of Pelizaeus-Merzbacher disease: metabolic abnormalities as diagnostic tools
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