Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes (Q38151554)

29 August 2017

title

Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes (English)

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autosomal recessive polycystic kidney

29 August 2017

main subject

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author name string

Rainer Büscher

1

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29 August 2017

Anja K Büscher

2

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29 August 2017

Stefanie Weber

3

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29 August 2017

Julia Mohr

4

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29 August 2017

Bianca Hegen

5

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29 August 2017

Udo Vester

6

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29 August 2017

Peter F Hoyer

7

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29 August 2017

publication date

10 October 2013

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29 August 2017

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29 August 2017

volume

29

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29 August 2017

issue

10

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29 August 2017

page(s)

1915-1925

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Genetics and pathogenesis of polycystic kidney disease.

29 August 2017

cites work

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

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

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New approaches to the autosomal recessive polycystic kidney disease patient with dual kidney-liver complications

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Hepatorenal findings in obligate heterozygotes for autosomal recessive polycystic kidney disease

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Abnormal lung development precedes oligohydramnios in a transgenic murine model of renal dysgenesis.

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The mTOR pathway is regulated by polycystin-1, and its inhibition reverses renal cystogenesis in polycystic kidney disease

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Pasireotide is more effective than octreotide in reducing hepatorenal cystogenesis in rodents with polycystic kidney and liver diseases.

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Inhibition of mTOR with sirolimus does not attenuate progression of liver and kidney disease in PCK rats

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Autosomal recessive polycystic kidney disease in adulthood

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Intracranial aneurysms in a child with autosomal recessive polycystic kidney disease

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Intracranial aneurysm and recessive polycystic kidney disease: the third reported case.

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Milder Presentation of Recessive Polycystic Kidney Disease Requires Presence of Amino Acid Substitution Mutations

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12 December 2020

Intrahepatic biliary cystic lesions

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12 December 2020

Nephrectomy in an autosomal recessive polycystic kidney disease (ARPKD) patient with rapid kidney enlargement and increased expression of EGFR

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12 December 2020

Cystic renal diseases in children

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12 December 2020

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12 December 2020

Autosomal dominant polycystic kidney disease

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12 December 2020

Multiple intracranial aneurysms in a patient with autosomal recessive polycystic kidney disease

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12 December 2020

Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology

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12 December 2020

Combined liver and kidney transplantation in children

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12 December 2020

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12 December 2020

Autosomal recessive polycystic kidney disease

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12 December 2020

Chronic renal failure and portal hypertension--is portosystemic shunt indicated?

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12 December 2020

Inhibition of renal cystic disease development and progression by a vasopressin V2 receptor antagonist

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12 December 2020

Therapies to slow polycystic kidney disease

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12 December 2020

Clinical aspects of autosomal recessive polycystic kidney disease

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12 December 2020

Structure and function of the pancreas in the polycystic kidney rat

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12 December 2020

Ultrasonographic study of pancreatic cysts in autosomal dominant polycystic kidney disease.

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12 December 2020

10.1007/S00467-013-2634-1

Identifiers

DOI

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Dimensions Publication ID

29 August 2017

1047159321

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