(Q34198423)

31 July 2017

title

Von Hippel-Lindau disease masquerading as autosomal dominant polycystic kidney disease (English)

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autosomal dominant polycystic kidney disease

31 July 2017

main subject

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von Hippel-Lindau disease

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autosomal dominant polycystic kidney

inferred from title

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Chatha RK

1

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31 July 2017

Johnson AM

2

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31 July 2017

Rothberg PG

3

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31 July 2017

Townsend RR

4

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31 July 2017

Neumann HP

5

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31 July 2017

Gabow PA

6

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31 July 2017

publication date

1 April 2001

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American Journal of Kidney Diseases

31 July 2017

published in

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31 July 2017

volume

37

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31 July 2017

issue

4

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31 July 2017

page(s)

852-858

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Autosomal dominant polycystic kidney disease

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

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

1 reference

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7 January 2021

A deletion polymorphism due to Alu-Alu recombination in intron 2 of the retinoblastoma gene: association with human gliomas

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Processed pseudogene from the von Hippel-Lindau disease gene is located on human chromosome 1

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

A genetic register for von Hippel-Lindau disease

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Renal cysts, renal cancer and von Hippel-Lindau disease

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Islet cell tumors in von Hippel-Lindau disease: increased prevalence and relationship to the multiple endocrine neoplasias

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

von Hippel-Lindau disease: radiologic screening for visceral manifestations

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

von Hippel-Lindau disease: genetic, clinical, and imaging features

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Von Hippel-Lindau disease: new strategies in early detection and treatment

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Renal involvement in von Hippel-Lindau disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

The prevalence and characterization of simple hepatic cysts by ultrasound examination

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Endolymphatic sac tumors. A source of morbid hearing loss in von Hippel-Lindau disease

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

von Hippel-Lindau disease affecting 43 members of a single kindred

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Treatment of renal cell carcinoma in von Hippel-Lindau disease: a multicenter study

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

The natural history of renal lesions in von Hippel-Lindau disease: a serial CT study in 28 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Intracranial aneurysms in patients with autosomal dominant polycystic kidney disease: how to diagnose and who to screen

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Autosomal dominant polycystic kidney disease: presentation, complications, and prognosis

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Pancreatic lesions in von Hippel-Lindau disease: prevalence, clinical significance, and CT findings

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Chronic obstructive pancreatitis due to a pancreatic cyst in a patient with autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Association between pancreatic cystadenocarcinoma, malignant liver cysts, and polycystic disease of the kidney

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

Von Hippel-Lindau disease: an important differential diagnosis of polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980136-0

7 January 2021

10.1016/S0272-6386(01)80136-0

Identifiers

DOI

1 reference

31 July 2017

1 reference