(Q33852423)

29 July 2017

title

Comparison of phenotypes of polycystic kidney disease types 1 and 2. European PKD1-PKD2 Study Group (English)

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polycystic kidney disease

29 July 2017

main subject

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N Hateboer

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29 July 2017

M A v Dijk

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29 July 2017

N Bogdanova

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29 July 2017

E Coto

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29 July 2017

A K Saggar-Malik

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29 July 2017

J L San Millan

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29 July 2017

R Torra

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29 July 2017

M Breuning

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29 July 2017

D Ravine

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29 July 2017

language of work or name

English

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publication date

1 January 1999

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29 July 2017

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29 July 2017

volume

353

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29 July 2017

issue

9147

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29 July 2017

page(s)

103-107

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Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney disease

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903495-3

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Autosomal dominant polycystic kidney disease

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The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16. The European Polycystic Kidney Disease Consortium

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https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903495-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903495-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903495-3

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PKD1 interacts with PKD2 through a probable coiled-coil domain

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https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903495-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903495-3

7 January 2021

Genetic Heterogeneity of Polycystic Kidney Disease in Europe1

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The diagnosis and prognosis of autosomal dominant polycystic kidney disease

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7 January 2021

Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease

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https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903495-3

7 January 2021

DNA microsatellite analysis of families with autosomal dominant polycystic kidney disease types 1 and 2: evaluation of clinical heterogeneity between both forms of the disease

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Counselling under genetic heterogeneity: a practical approach.

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

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7 January 2021

Components of blood pressure and risk of atherothrombotic brain infarction: the Framingham study

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Progression of renal insufficiency: role of blood pressure

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7 January 2021

Influence of hypertension on early renal insufficiency in autosomal dominant polycystic kidney disease

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7 January 2021

Clinical profiles of gross hematuria in autosomal dominant polycystic kidney disease

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7 January 2021

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

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7 January 2021

End-stage renal failure appears earlier in men than in women with polycystic kidney disease

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7 January 2021

Autosomal dominant polycystic kidney disease: new information for genetic counselling

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7 January 2021

Effects of sex hormones on fluid and solute transport in Madin-Darby canine kidney cells

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7 January 2021

Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory

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Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie

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A century of mortality in five large families with polycystic kidney disease

1 reference

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7 January 2021

10.1016/S0140-6736(98)03495-3

Identifiers

DOI

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29 July 2017

1 reference