Polycystic disease of kidney and liver presenting in childhood
about
Evidence for a "Pathogenic Triumvirate" in Congenital Hepatic Fibrosis in Autosomal Recessive Polycystic Kidney DiseaseDifferential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesionChlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagellaAutosomal recessive polycystic kidney disease: antenatal diagnosis and histopathological correlation.Comments upon the classification of infantile polycystic diseases of the liver and kidney, based upon three-dimensional reconstruction of the liver.Monogenic disorders.Polycystic kidney disease in children: a genetic and epidemiological study of 82 Finnish patients.Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease.Surgical management of polycystic liver diseaseThe severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counseling.Oval cell proliferation associated with the murine insertional mutation TgN737Rpw.Three cases of congenital hepatic fibrosis with Caroli's disease in three siblings.A complex case of congenital cystic renal diseaseExperimental infantile polycystic kidney in rats. The influence of age and sex.Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease.Congenital hepatic fibrosis and adult-type autosomal dominant polycystic kidney disease in a childJuvenile hepatic fibropolycystic disease and other abnormalities.Developments in the management of autosomal dominant polycystic kidney disease.New approaches to the autosomal recessive polycystic kidney disease patient with dual kidney-liver complications.Cortical microcystic disease of the kidney with dominant inheritance: a previously undescribed syndrome.Pathophysiology, epidemiology, classification and treatment options for polycystic liver diseasesCongenital hepatic fibrosis.Juvenile nephronophthisis associated with skeletal abnormalities and hepatic fibrosis.Congenital hepatic fibrosis leading to cirrhosis and hepatocellular carcinoma: a case report.Screening for polycystic kidney disease: importance of clinical presentation in the newborn.
P2860
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P2860
Polycystic disease of kidney and liver presenting in childhood
description
1971 nî lūn-bûn
@nan
1971 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1971 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1971年の論文
@ja
1971年学术文章
@wuu
1971年学术文章
@zh-cn
1971年学术文章
@zh-hans
1971年学术文章
@zh-my
1971年学术文章
@zh-sg
1971年學術文章
@yue
name
Polycystic disease of kidney and liver presenting in childhood
@ast
Polycystic disease of kidney and liver presenting in childhood
@en
Polycystic disease of kidney and liver presenting in childhood
@nl
type
label
Polycystic disease of kidney and liver presenting in childhood
@ast
Polycystic disease of kidney and liver presenting in childhood
@en
Polycystic disease of kidney and liver presenting in childhood
@nl
prefLabel
Polycystic disease of kidney and liver presenting in childhood
@ast
Polycystic disease of kidney and liver presenting in childhood
@en
Polycystic disease of kidney and liver presenting in childhood
@nl
P2860
P1476
Polycystic disease of kidney and liver presenting in childhood
@en
P2093
P2860
P304
P407
P577
1971-09-01T00:00:00Z