Search Results - "Liapi, Olga"

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  1. 1

    Observations in febrile children with round air space opacities by Fretzayas, Andrew, Moustaki, Maria, Alexopoulou, Efthimia, Liapi, Olga, Nicolaidou, Polyxeni, Priftis, Konstantinos N.

    Published in Pediatrics international (01-06-2010)
    “…Background:  Community‐acquired pneumonia in children is rarely depicted as round opacity. The aim of the present study was therefore to describe the clinical…”
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    Journal Article
  2. 2

    Is Ceftriaxone-Induced Biliary Pseudolithiasis Influenced by UDP-Glucuronosyltransferase 1A1 Gene Polymorphisms? by Fretzayas, Andrew, Liapi, Olga, Papadopoulou, Anna, Nicolaidou, Polyxeni, Stamoulakatou, Alexandra

    Published in Case Reports in Medicine (01-01-2011)
    “…Ceftriaxone (cfx), a third-generation cephalosporin antibiotic, leads to transient cholelithiasis in some children, also known as pseudolithiasis. However, the…”
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    Journal Article
  3. 3

    Erythema Nodosum in a Child with Celiac Disease by Fretzayas, Andrew, Moustaki, Maria, Liapi, Olga, Nicolaidou, Polyxeni

    Published in Case reports in pediatrics (01-01-2011)
    “…Erythema nodosum is an acute, nodular, erythematous eruption usually limited to the extensor aspects of the lower legs. It could be idiopathic or associated…”
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    Journal Article
  4. 4

    Eponym: Gilbert syndrome by Fretzayas, Andrew, Moustaki, Maria, Liapi, Olga, Karpathios, Themistocles

    Published in European journal of pediatrics (2012)
    “…Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unconjugated…”
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    Journal Article
  5. 5

    Eponym by Fretzayas, Andrew, Moustaki, Maria, Liapi, Olga, Karpathios, Themistocles

    Published in European journal of pediatrics (01-01-2012)
    “…Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unconjugated…”
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    Journal Article
  6. 6

    Gilbert syndrome by Fretzayas, Andrew, Moustaki, Maria, Liapi, Olga, Karpathios, Themistocles

    Published in European journal of pediatrics (01-01-2012)
    “…Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unconjugated…”
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    Journal Article
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