Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes. - Wikidata - awgldk - TriplyDB

Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes.

Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes.

http://www.wikidata.org/entity/Q38151554

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Inhibition of MiR-199a-5p reduced cell proliferation in autosomal dominant polycystic kidney disease through targeting CDKN1C.Rationale, design and objectives of ARegPKD, a European ARPKD registry study Liver involvement in kidney disease and vice versa.Long-term pulmonary function in children with recessive polycystic kidney disease.Rare diseases, rare presentations: recognizing atypical inherited kidney disease phenotypes in the age of genomics Network for Early Onset Cystic Kidney Diseases-A Comprehensive Multidisciplinary Approach to Hereditary Cystic Kidney Diseases in Childhood.Aberrant transcriptional regulation could explain phenotypic variability in autosomal recessive polycystic kidney disease.Compound heterozygous PKHD1 variants cause a wide spectrum of ductal plate malformations.Autosomal Recessive Polycystic Kidney Disease.

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P2860

Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes.

http://www.wikidata.org/entity/Q38151554

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Clinical manifestations of aut ...... non-kidney-related phenotypes.

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Clinical manifestations of aut ...... non-kidney-related phenotypes.

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Pediatric Nephrology

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Clinical manifestations of aut ...... non-kidney-related phenotypes.

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Anja K Büscher

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Bianca Hegen

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Julia Mohr

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Peter F Hoyer

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Rainer Büscher

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Stefanie Weber

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Udo Vester

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P2860

Autosomal dominant polycystic kidney disease: the last 3 years

Potential pharmacological interventions in polycystic kidney disease

Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF).

Genetics and pathogenesis of polycystic kidney disease.

Characteristics of congenital hepatic fibrosis in a large cohort of patients with autosomal recessive polycystic kidney disease.

The mTOR pathway is regulated by polycystin-1, and its inhibition reverses renal cystogenesis in polycystic kidney disease

The spectrum of polycystic kidney disease in children.

Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease.

Hepatorenal findings in obligate heterozygotes for autosomal recessive polycystic kidney disease.

Liver disease in autosomal recessive polycystic kidney disease.

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s00467-013-2634-1

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1915-1925

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10.1007/S00467-013-2634-1

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2013-10-10T00:00:00Z

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P921

Autosomal recessive polycystic kidney