Kidney and liver transplantation in patients with autosomal recessive polycystic kidney disease: a multicentric study. (Q43803985)

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16 January 2020

title

Kidney and liver transplantation in patients with autosomal recessive polycystic kidney disease: a multicentric study (English)

1 reference

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autosomal recessive polycystic kidney

16 January 2020

main subject

0 references

liver transplantation

1 reference

6

1 reference

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16 January 2020

author name string

Marion Chapal

1

1 reference

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16 January 2020

Agnès Debout

2

1 reference

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16 January 2020

Alexandre Dufay

3

1 reference

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16 January 2020

Rémi Salomon

4

1 reference

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16 January 2020

Gwenaelle Roussey

5

1 reference

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16 January 2020

Emma Allain Launay

7

1 reference

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16 January 2020

Cécile Vigneau

8

1 reference

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16 January 2020

Gilles Blancho

9

1 reference

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16 January 2020

Chantal Loirat

10

1 reference

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16 January 2020

Maryvonne Hourmant

11

1 reference

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16 January 2020

Fadi Fakhouri

12

1 reference

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16 January 2020

language of work or name

English

0 references

publication date

9 November 2011

1 reference

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Nephrology Dialysis Transplantation

16 January 2020

published in

1 reference

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16 January 2020

volume

27

1 reference

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16 January 2020

issue

5

1 reference

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16 January 2020

page(s)

2083-2088

1 reference

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Polycystic kidney disease

16 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

Abnormalities in focal adhesion complex formation, regulation, and function in human autosomal recessive polycystic kidney disease epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

Long-term renal function in children after liver transplantation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

Autosomal recessive polycystic kidney disease in adulthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

Polycystic disease of the liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

Congenital diseases of intrahepatic bile ducts: variations on the theme "ductal plate malformation"

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

Congenital dilatation of the intrahepatic bile ducts associated with the development of amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588

Caroli's disease and outcomes after liver transplantation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFR588