Extrarenal manifestations of ADPKD. (Q41501269)

1 October 2017

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title

Extrarenal manifestations of ADPKD. (English)

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1 October 2017

Perrone RD

1

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PubMed ID

9186898

1 October 2017

language of work or name

English

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publication date

1 June 1997

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1 October 2017

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1 October 2017

51

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1 October 2017

6

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1 October 2017

2022-2036

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https://scigraph.springernature.com/pub.10.1038/ki.1997.276

1 October 2017

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cites work

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A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

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Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

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Evidence for a third genetic locus for autosomal dominant polycystic kidney disease

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Polycystic kidney disease: The complete structure of the PKD1 gene and its protein

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The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains

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Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat. The American PKD1 Consortium (APKD1 Consortium)

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PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

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Frequency of hepatic cysts in adult polycystic kidney disease

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Risk factors for the development of hepatic cysts in autosomal dominant polycystic kidney disease

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Hepatic cysts in autosomal dominant polycystic kidney disease

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Liver cysts in patients with autosomal dominant polycystic kidney disease

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Is gender a determinant for evolution of renal failure? A study in autosomal dominant polycystic kidney disease

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Hepatic cyst infection in autosomal dominant polycystic kidney disease

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Polycystic liver disease: quantitation of parenchymal and cyst volumes from computed tomography images and clinical correlates of hepatic cysts

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Liver resection and cyst fenestration in the treatment of severe polycystic liver disease

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Hepatic cysts in autosomal dominant polycystic kidney disease

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Treatment of highly symptomatic polycystic liver disease. Preliminary experience with a combined hepatic resection-fenestration procedure

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Liver transplantation for polycystic liver disease

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Surgical management of nonparasitic cystic liver disease

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Highly symptomatic adult polycystic disease of the liver. A report of fifteen cases

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Polycystic liver disease with obstructive jaundice: treatment with ultrasound-guided cyst aspiration

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Hepatic venous outflow obstruction in patients with polycystic liver disease: pathogenesis and treatment

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Regression of large hepatic cysts by minocycline hydrochloride in polycystic kidney disease

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Budd-Chiari syndrome following pretransplantation nephrectomy in an ADPKD patient with liver cysts

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Budd-Chiari syndrome in autosomal dominant polycystic kidney disease: a complication of nephrectomy in patients with liver cysts

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Surgery for adult polycystic liver disease

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Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease

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Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2

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Occult intracranial aneurysms in polycystic kidney disease. When is cerebral arteriography indicated?

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Intracranial aneurysm in adult polycystic kidney disease: is screening with MR angiography indicated?

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Screening for unruptured intracranial aneurysms in autosomal dominant polycystic kidney disease

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Recurrent rupture of intracranial aneurysms in autosomal dominant polycystic kidney disease

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Intracranial aneurysms in autosomal dominant polycystic kidney disease

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Vessel malformation in a patient with ADPKD: megadolichobasilar artery, abdominal aortic and iliac aneurysms

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Coronary artery aneurysms in association with adult polycystic kidney disease

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Spontaneous vertebral artery dissection as a complication of autosomal dominant polycystic kidney disease

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Cardiovascular Abnormalities Associated with Adult Polycystic Kidney Disease

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Autosomal dominant polycystic kidney disease with liver and pancreatic involvement in early childhood

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Adult polycystic renal disease presenting in infancy: a report emphasizing the bilateral involvement

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Renal replacement therapy in autosomal dominant polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Clinical aspects of polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD 1 locus

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

A second genetic locus for autosomal dominant polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Association of congenital hepatic fibrosis with autosomal dominant polycystic kidney disease. Report of a family with review of literature

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Intracranial cysts in autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Left ventricular mass in normotensive subjects with autosomal dominant polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Renal, cardiovascular and hormonal characteristics of young adults with autosomal dominant polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

The cystic fibrosis transmembrane conductance regulator mediates transepithelial fluid secretion by human autosomal dominant polycystic kidney disease epithelium in vitro

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndrome

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Apoptosis and loss of renal tissue in polycystic kidney diseases

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Attitudes of at-risk and affected individuals regarding presymptomatic testing for autosomal dominant polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Matrix metalloproteinase activity in human intrahepatic biliary epithelial cell lines from patients with autosomal dominant polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

What, if any, is the appropriate neurological work-up for a child with autosomal dominant polycystic kidney disease and a family history of intra-cranial aneurysm?

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Polycystin, the polycystic kidney disease 1 protein, is expressed by epithelial cells in fetal, adult, and polycystic kidney

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Hepatobiliary complications of oral contraceptives

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1.

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Gastrointestinal complications after renal transplantation

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Colon perforation in renal transplant patients

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Colon Perforation After Kidney Transplantation

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Long-term outcome of renal transplantation in autosomal dominant polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Long-term cardiovascular morbidity and mortality in autosomal dominant polycystic kidney disease patients after renal transplantation

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Stroke in renal transplant recipients.

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https://api.crossref.org/works/10.1038%2FKI.1997.276

7 January 2021

Identifiers

DOI

10.1038/KI.1997.276

1 reference

1 October 2017

1 reference

PubMed ID

9186898