(Q38725128)

5 September 2017

1 reference

title

Polycystic kidney diseases in childhood (English)

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5 September 2017

1 reference

Kaplan BS

1

1 reference

5 September 2017

Kaplan P

2

1 reference

5 September 2017

Rosenberg HK

3

1 reference

5 September 2017

Lamothe E

4

1 reference

5 September 2017

Rosenblatt DS

5

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5 September 2017

language of work or name

English

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publication date

1 December 1989

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The Journal of Pediatrics

5 September 2017

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5 September 2017

115

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5 September 2017

867-880

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5 September 2017

6

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Pathogenesis of human cystic renal disease

5 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Autosomal recessive polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Variable expression of autosomal recessive polycystic kidney disease and congenital hepatic fibrosis within a family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Polycystic kidney disease in the first year of life

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Polycystic disease and hepatic fibrosis in children. Renal function studies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Hypertension in infantile polycystic renal disease. The importance of early recognition and treatment of severe hypertension in polycystic renal disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Congenital hepatic fibrosis in children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Cystic diseases of the kidney--radiological and pathological considerations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Congenital hepatic fibrosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

The sonographic distinction between neonatal multicystic kidney and hydronephrosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

The diagnosis of congenital renal anomalies with ultrasound. II. Infantile polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Autosomal recessive polycystic kidney disease. Problems of prenatal diagnosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Infantile polycystic kidney disease: observations from attempts at prenatal diagnosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Prenatal detection of the autosomal recessive type of polycystic kidney disease by trehalase assay in amniotic fluid

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Cystic disease of the kidneys. Autopsy report and family study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

The renal lesion of congenital hepatic fibrosis: pathologic and morphometric analysis, with comparison to the renal lesion of infantile polycystic disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Infantile polycystic disease of the kidneys and liver: clinical, pathological and radiological correlations and comparison with congenital hepatic fibrosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Cystic disease of the kidney in the newborn infant

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

The spectrum of polycystic disease in children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Prenatal diagnosis of an early manifestation of autosomal dominant adult-type polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Infantile presentation of adult-type polycystic kidney disease in a large kindred

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Autosomal dominant polycystic renal disease in children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Autosomal dominant polycystic kidney disease in childhood: a longitudinal study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Polycystic kidney disease: prospective analysis of nonazotemic patients and family members

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Ultrasound for genetic counselling in polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Prenatal diagnosis of adult polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Unilateral abdominal mass: an unusual presentation of autosomal dominant polycystic kidney disease in children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Ultrasonography and nephrotomography in the presymptomatic diagnosis of dominantly inherited (adult-onset) polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Renal cysts in polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Cyst formation and growth in autosomal dominant polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Adult dominant polycystic kidney disease--clinical problems

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

A study of genetic linkage heterogeneity in adult polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

A second genetic locus for autosomal dominant polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Regional localization of the autosomal dominant polycystic kidney disease locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Renal infections in autosomal dominant polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Prenatal diagnosis of autosomal dominant polycystic kidney disease with a DNA probe

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Attitudes to early diagnosis of polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Age at clinical onset and at ultrasonographic detection of adult polycystic kidney disease: data for genetic counselling

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Prognosis of adult onset polycystic kidney disease re-evaluated

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Chemical modification of cell proliferation and fluid secretion in renal cysts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Screening for polycystic kidney disease: importance of clinical presentation in the newborn

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Bleeding esophageal varices with polycystic liver; report of three cases.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Polycystic kidney disease of perinatal type

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly"

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Familial juvenile nephronophthisis, Jeune's syndrome, and associated disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Renal-hepatic-pancreatic dysplasia: a syndrome reconsidered

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Cortical microcystic disease of the kidney with dominant inheritance: a previously undescribed syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Familial adult glomerulocystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Ultrasonographic features of glomerulocystic disease in infancy: similarity to infantile polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Possible new autosomal recessive syndrome with unusual renal histopathological changes

7 January 2021

2 references

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

inferred from DOI database lookup

7 January 2021

based on heuristic

Congenital hypernephronic nephromegaly with tubular dysgenesis: a distinctive inherited renal anomaly

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Isolated congenital renal tubular immaturity in siblings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Renal tubular dysgenesis: delayed onset of oligohydramnios

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

Polycystic disease of kidney and liver presenting in childhood

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

inferred from DOI database lookup

7 January 2021

based on heuristic

Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980735-8

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(89)80735-8

1 reference

5 September 2017

1 reference