Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney? - Wikidata - wikimedia - TriplyDB

Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?

Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?

http://www.wikidata.org/entity/Q38239257

about

Proposal for an algorithm for liver transplantation in Caroli's disease and syndrome: putting an uncommon effort into a common task.Combined liver and kidney transplantation and kidney after liver transplantation in children: Indication, postoperative outcome, and long-term results.

P2860

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P2860

Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?

http://www.wikidata.org/entity/Q38239257

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

@zh-cn

name

Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?

@en

type

label

Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?

@en

prefLabel

Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?

@en

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S00467-014-2887-3

P1433

Pediatric Nephrology

P1476

Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?

@en

P2093

Akin Tekin

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

Jayanthi Chandar

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

Jennifer Garcia

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

Lydia Jorge

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

P2860

Fibrocystin/polyductin modulates renal tubular formation by regulating polycystin-2 expression and function

Combined liver-kidney transplantation for primary hyperoxaluria type 1 in young children.

Cell salvage as part of a blood conservation strategy in anaesthesia.

A single-institution review of portosystemic shunts in children: an ongoing discussion.

Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease.

Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference

Characteristics of congenital hepatic fibrosis in a large cohort of patients with autosomal recessive polycystic kidney disease.

Liver transplantation in patients with previous portasystemic shunt.

Caroli's disease: identification and treatment strategy.

Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease.

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s00467-014-2887-3

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1233-1242

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scholarly article

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10.1007/S00467-014-2887-3

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8

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30

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264797328

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1022416315

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25115876

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P921

Autosomal recessive polycystic kidney