Coexistence of gilbert syndrome and hereditary spherocytosis in a child presenting with extreme jaundice.

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New insights on hereditary erythrocyte membrane defects How to apply clinical cases and medical literature in the framework of a modified "failure mode and effects analysis" as a clinical reasoning tool--an illustration using the human biliary system.

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Coexistence of gilbert syndrome and hereditary spherocytosis in a child presenting with extreme jaundice.

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2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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2014年论文

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2014年论文

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name

Coexistence of gilbert syndrom ...... senting with extreme jaundice.

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Coexistence of gilbert syndrom ...... senting with extreme jaundice.

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Coexistence of gilbert syndrom ...... senting with extreme jaundice.

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P1476

Coexistence of gilbert syndrom ...... senting with extreme jaundice.

@en

P2093

Jae Hee Lee

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Kyung Rye Moon

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P2860

Population studies on Gilbert's syndrome

Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis.

High incidence of early cholelithiasis detected by ultrasonography in children and young adults with hereditary spherocytosis.

Hereditary spherocytosis.

Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome.

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

A case of concomitant Gilbert's syndrome and hereditary spherocytosis.

Gilbert syndrome.

A Case of hereditary spherocytosis coexisting with Gilbert's syndrome.

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266-269

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scholarly article

case report

P356

10.5223/PGHN.2014.17.4.266

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2014-12-31T00:00:00Z

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270909223

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25587528

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4291453

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Coexistence of gilbert syndrome and hereditary spherocytosis in a child presenting with extreme jaundice.

about

P2860

P2860

Coexistence of gilbert syndrome and hereditary spherocytosis in a child presenting with extreme jaundice.

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