Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The natural history of autosomal dominant polycystic kidney disease. A strategy for grouping families and mutations.

Nefrologia - 1 Jan 2000

Espinosa Cabello Mario, Ansio Vázquez Inmaculada, Espejo Portero Isabel, Rodriguez Fuentes David, Rabasco Ruiz Cristina, Espinosa Hernández Mario

Abstract excerpt

Autosomal dominant polycystic kidney disease (ADPKD) is a main cause of end-stage renal disease. Today, knowledge of its genetic basis has made it possible to develop strategies that prevent the transmission of the disease. OBJECTIVES: The objective of the study was to analyze the natural history of ADPKD in the province of Córdoba and to design a database that allows grouping families with different mutations....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic and Kidney Cyst Diseases
Share to Kidney

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Polycystic Kidney, Autosomal Dominant

Share to Renal and related cancers

Share to Renal Diseases and Glomerulopathies

Share to TRPP Cation Channels

Source

Identifiers

PMID: 37268502
DOI: 10.1016/j.nefroe.2023.03.010

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The natural history of autosomal dominant polycystic kidney disease. A strategy for grouping families and mutations.PMID 37268502Read ↗

Autosomal dominant polycystic kidney disease (ADPKD) in Tunisia: From molecular genetics to the development of prognostic tools.Semantic proximity Read ↗

Mutational Screening of PKD1 and PKD2 Genes in Iranian Population Diagnosed with Autosomal Dominant Polycystic Kidney Disease.Semantic proximity Read ↗

Clinical and Genetic Characteristics of Autosomal Recessive Polycystic Kidney Disease in OmanSemantic proximity Read ↗

New mutation associated with autosomal dominant polycystic kidney disease with founder effect located in the alpujarra region of granada.Semantic proximity Read ↗

Co-Inheritance of Pathogenic Variants in PKD1 and PKD2 Genes Determined by Parental Segregation and De Novo Origin: A Case Report.Semantic proximity Read ↗

Mutational analysis in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD): Identification of five mutations in the PKD1 gene.Semantic proximity Read ↗

Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in OmanSemantic proximity Read ↗

Identification of Pathogenic PKHD1 Variants in Infants with Autosomal Recessive Polycystic Kidney Disease from the Dhofar Region, OmanSemantic proximity Read ↗

Identification of Pathogenic PKHD1 Variants in Infants with Autosomal Recessive Polycystic Kidney Disease from the Dhofar Region, OmanSemantic proximity Read ↗

Genetic Characteristics of Korean Patients with Autosomal Dominant Polycystic Kidney Disease by Targeted Exome Sequencing.Semantic proximity Read ↗

Molecular genetics of autosomal dominant polycystic kidney disease.Semantic proximity Read ↗

Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD).Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.