Literature DB >> 14631626

Simultaneous presence of Gilbert syndrome and hereditary spherocytosis: interaction in the pathogenesis of hyperbilirubinemia and gallstone formation.

Marina Economou, Ioanna Tsatra, Miranda Athanassiou-Metaxa.   

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Year:  2003        PMID： 14631626

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN： 0888-0018            Impact factor:   1.969


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  1 in total

1.  Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.

Authors:  Shigeo Iijima; Takehiko Ohzeki; Yoshihiro Maruo
Journal:  Yonsei Med J       Date:  2011-03       Impact factor: 2.759
  1 in total

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