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

Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.

Kidney international - 1 Jan 2000

Norden A G, Scheinman S J, Deschodt-Lanckman M M, Lapsley M, Nortier J L, Thakker R V, Unwin R J, Wrong O

Abstract excerpt

UNLABELLED: Tubular proteinuria defined by a study of Dent's ( CLCN5 mutation) and other tubular diseases. BACKGROUND: The term "tubular proteinuria" is often used interchangeably with "low molecular weight proteinuria" (LMWP), although the former implies a definite etiology. A specific quantitat...

Read the complete abstract on PubMed

Topics

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

Share to Chloride Channels
Share to Drugs, Chinese Herbal
Share to Glomerulonephritis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hematuria

Share to Kidney Diseases

Share to Kidney Tubules

Share to Molecular Weight

Share to Proteinuria

Source

Identifiers

PMID: 10620205
DOI: 10.1046/j.1523-1755.2000.00847.x

Genes

CLCN5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-10620205-2026-09-02.2. 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

Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.PMID 10620205Read ↗

Proteinuria in Dent disease: a review of the literature.Semantic proximity Read ↗

Japanese Dent disease has a wider clinical spectrum than Dent disease in Europe/USA: genetic and clinical studies of 86 unrelated patients with low-molecular-weight proteinuria.Semantic proximity Read ↗

A Focus on the Proximal Tubule Dysfunction in Dent Disease Type 1.Semantic proximity Read ↗

Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.Semantic proximity Read ↗

Predicting the protein composition of human urine in normal and pathological states: Quantitative description based on Dent1 disease (CLCN5 mutation).Semantic proximity Read ↗

From protein uptake to Dent disease: An overview of the CLCN5 gene.Semantic proximity Read ↗

[Dent disease (idiopathic tubular proteinuria): Pathogenesis, pathophysiology, and therapy].Semantic proximity Read ↗

Expanding the phenotype of proteinuria in Dent disease. A case series.Semantic proximity Read ↗

Clinical and genetic characteristics of Dent's disease type 1 in Europe.Semantic proximity Read ↗

Dent's disease: clinical features and molecular basis.Semantic proximity Read ↗

A Focus on the Metabolic Dysfunction of Proximal Tubule Cells in Dent Disease Type 1Semantic proximity Read ↗

Genetic and clinical phenotype of Dent disease in Chinese children and the etiological analysis of early - onset chronic kidney disease.Semantic proximity Read ↗

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