Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.

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Gilbert syndrome combined with prolonged jaundice caused by contrast agent: Case report.

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Q52597719-CEF09E05-CA75-40F6-A058-AF75516EEA54

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Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.

Item

http://www.wikidata.org/entity/Q42290117

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Gilbert Syndrome with Concomit ...... conjugated Hyperbilirubinemia.

@en

Gilbert Syndrome with Concomit ...... conjugated Hyperbilirubinemia.

@nl

type

Item

label

Gilbert Syndrome with Concomit ...... conjugated Hyperbilirubinemia.

@en

Gilbert Syndrome with Concomit ...... conjugated Hyperbilirubinemia.

@nl

prefLabel

Gilbert Syndrome with Concomit ...... conjugated Hyperbilirubinemia.

@en

Gilbert Syndrome with Concomit ...... conjugated Hyperbilirubinemia.

@nl

P1476

Gilbert Syndrome with Concomit ...... conjugated Hyperbilirubinemia.

@en

P2093

Atsushi Tanaka

http://www.w3.org/2001/XMLSchema#string

Hajime Takikawa

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Kotaro Miura

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Minami Yagi

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Mitsuhiko Aiso

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Ryo Miura

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Sayuri Nakahara

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Toshihiko Arizumi

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Yoriyuki Takamori

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Yoshihiro Maruo

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P2860

Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II

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

The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.

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

Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes.

Risks and benefits of splenectomy versus no splenectomy for hereditary spherocytosis--a personal view.

Hereditary spherocytosis coexisting with Gilbert's syndrome: a diagnostic dilemma.

[Study on the mechanisms of diarrhea induced by a new anticancer camptothecin derivative, irinotecan hydrochloride (CPT-11), in rats].

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661-664

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P31

scholarly article

case report

P356

10.2169/INTERNALMEDICINE.56.7362

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2017-03-17T00:00:00Z

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P698

28321066

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P921

bilirubin metabolic disorder

P932

5410476

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Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.

about

P2860

P2860

Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.

description

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932