Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Olga, Liapi"'
Publikováno v:
Case Reports in Pediatrics, Vol 2011 (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 with other systemic diseases. We, herein, report a phenotypically healthy, ten-year-old boy w
Externí odkaz:
https://doaj.org/article/25f61ffc98134395ad9143ba00084eb6
Autor:
Andrew Fretzayas, Olga Liapi, Anna Papadopoulou, Polyxeni Nicolaidou, Alexandra Stamoulakatou
Publikováno v:
Case Reports in Medicine, Vol 2011 (2011)
Ceftriaxone (cfx), a third-generation cephalosporin antibiotic, leads to transient cholelithiasis in some children, also known as pseudolithiasis. However, the underlying pathogenetic mechanism of this adverse effect has not yet been elucidated. We d
Externí odkaz:
https://doaj.org/article/ccf70ab0ad974a9083b33b5d22eaf67a
Publikováno v:
European Journal of Pediatrics. 171:11-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::637dfc2c844dd9391a58b9b1954c8bb5
https://doi.org/10.1007/s00431-011-1641-0
https://doi.org/10.1007/s00431-011-1641-0
Autor:
Anna Papadopoulou, Polyxeni Nicolaidou, Olga Liapi, Alexandra Stamoulakatou, Andrew Fretzayas
Publikováno v:
Case Reports in Medicine, Vol 2011 (2011)
Case Reports in Medicine
Case Reports in Medicine
Ceftriaxone (cfx), a third-generation cephalosporin antibiotic, leads to transient cholelithiasis in some children, also known as pseudolithiasis. However, the underlying pathogenetic mechanism of this adverse effect has not yet been elucidated. We d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc46ee98029e76241a365e26c08afb46
https://doi.org/10.1155/2011/730250
https://doi.org/10.1155/2011/730250
Autor:
Olga Liapi, Maria Moustaki, Konstantinos N. Priftis, Polyxeni Nicolaidou, Efthimia Alexopoulou, Andrew Fretzayas
Publikováno v:
Pediatrics International. 52:444-446
Background: Community-acquired pneumonia in children is rarely depicted as round opacity. The aim of the present study was therefore to describe the clinical and laboratory characteristics of round pneumonia in children. Methods: The clinical series
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3eb310fa2ccfe7c3164713b3042fb472
https://doi.org/10.1111/j.1442-200x.2009.03004.x
https://doi.org/10.1111/j.1442-200x.2009.03004.x
Publikováno v:
European journal of pediatrics. 171(1)
Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unconjugated hyperbilirubinemia in the absence of hepatocellular disease or hemolysis. In patients with Gilbert syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::97f5666fe998476084cb48d13f8eb421
https://pubmed.ncbi.nlm.nih.gov/22160004
https://pubmed.ncbi.nlm.nih.gov/22160004
Autor:
Andrew, Fretzayas, Maria, Moustaki, Efthimia, Alexopoulou, Olga, Liapi, Polyxeni, Nicolaidou, Konstantinos N, Priftis
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 52(3)
Community-acquired pneumonia in children is rarely depicted as round opacity. The aim of the present study was therefore to describe the clinical and laboratory characteristics of round pneumonia in children.The clinical series consisted of 30 childr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8274080f46c6c74265b0c529ce457f19
https://pubmed.ncbi.nlm.nih.gov/19912554
https://pubmed.ncbi.nlm.nih.gov/19912554