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

Earlier diagnosis of autosomal dominant polycystic kidney disease: importance of family history and implications for cardiovascular and renal complications.

American journal of kidney diseases : the official journal of the National Kidney Foundation - 1 Sept 2005

Taylor Matthew, Johnson Ann M, Tison Maryellyn, Fain Pamela, Schrier Robert W

Abstract excerpt

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is a common and serious cause of hereditary renal disease. The emerging possibilities to intervene early in the disease course elevate the importance of both accurate and early diagnosis of ADPKD. Family history analysis is a simple...

Read the complete abstract on PubMed

Topics

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

Share to Cardiovascular Diseases
Share to Databases, Factual

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Early Diagnosis

Share to Family Health

Share to Health Surveys

Share to Kidney Failure, Chronic

Share to Polycystic Kidney, Autosomal Dominant

Share to Surveys and Questionnaires

Source

Identifiers

PMID: 16129202
DOI: 10.1053/j.ajkd.2005.05.029

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16129202-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Earlier diagnosis of autosomal dominant polycystic kidney disease: importance of family history and implications for cardiovascular and renal complications.PMID 16129202Read ↗

The PROPKD Score: A New Algorithm to Predict Renal Survival in Autosomal Dominant Polycystic Kidney Disease.Semantic proximity Read ↗

Incident renal events and risk factors in autosomal dominant polycystic kidney disease: a population and family-based cohort followed for 22 years.Semantic proximity Read ↗

Autosomal dominant polycystic kidney disease: new information for genetic counselling.Semantic proximity Read ↗

Variation in age at ESRD in autosomal dominant polycystic kidney disease.Semantic proximity Read ↗

Clinical utility of PKD2 mutation testing in a polycystic kidney disease cohort attending a specialist nephrology out-patient clinic.Semantic proximity Read ↗

Assessing the Risk of Progression to Kidney Failure in Patients With Autosomal Dominant Polycystic Kidney Disease.Semantic proximity Read ↗

Affected parent sex and severity of autosomal dominant polycystic kidney disease: a retrospective cohort study .Semantic proximity Read ↗

Presence of de novo mutations in autosomal dominant polycystic kidney disease patients without family history.Semantic proximity Read ↗

Autosomal dominant polycystic kidney disease types 1 and 2: assessment of US sensitivity for diagnosis.Semantic proximity Read ↗

Prenatal diagnosis of autosomal dominant polycystic kidney disease (PKD1) presenting in utero and prognosis for very early onset disease.Semantic proximity Read ↗

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

Clinicians’ attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney diseaseSemantic proximity Read ↗

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