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

Disappearance of tophi in familial juvenile hyperuricemic nephropathy after kidney transplantation.

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons - 1 Nov 2007

Merieau E, Al Najjar A, Halimi J-M, Sacquépée M, Nivet H, Lebranchu Y, Büchler M

Abstract excerpt

A 40-year-old man who had been on hemodialysis for 25 months due to familial juvenile hyperuricemic nephropathy (FJHN) received a kidney transplant. Biopsy of his native kidney had shown tubulo-interstitial nephropathy. Genetic analysis confirmed abnormal uromodulin expression due to a mutation i...

Read the complete abstract on PubMed

Topics

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

Share to Exons
Share to Gene Expression
Share to Hyperuricemia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Kidney Failure, Chronic

Share to Kidney Transplantation

Share to Mucoproteins

Share to Renal Dialysis

Share to Uromodulin

Source

Identifiers

PMID: 17868056
DOI: 10.1111/j.1600-6143.2007.01977.x

Genes

UMOD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17868056-2026-09-02.2. 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

Disappearance of tophi in familial juvenile hyperuricemic nephropathy after kidney transplantation.PMID 17868056Read ↗

Familial juvenile hyperuricemia in early childhood in a boy with a novel gene mutation.Semantic proximity Read ↗

Rare case of nephrocalcinosis in the distal tubules caused by hereditary renal hypouricaemia 3 months after kidney transplantation.Semantic proximity Read ↗

Chronic kidney disease in an adolescent with hyperuricemia: familial juvenile hyperuricemic nephropathy.Semantic proximity Read ↗

Novel UMOD mutations in familial juvenile hyperuricemic nephropathy lead to abnormal uromodulin intracellular trafficking.Semantic proximity Read ↗

Familial juvenile hyperuricemic nephropathy: detection of mutations in the uromodulin gene in five Japanese families.Semantic proximity Read ↗

Progressive accumulation of intrinsic mouse uromodulin in the kidneys of transgenic mice harboring the mutant human uromodulin gene.Semantic proximity Read ↗

A novel UMOD mutation (c.187T>C) in a Korean family with juvenile hyperuricemic nephropathy.Semantic proximity Read ↗

[Familial juvenile hyperuricemic nephropathy (FJHN)].Semantic proximity Read ↗

Apoptosis induced by an uromodulin mutant C112Y and its suppression by topiroxostat.Semantic proximity Read ↗

[Familial juvenile hyperuricemic nephropathy].Semantic proximity Read ↗

Outcome of kidney transplantation in familial juvenile hyperuricaemic nephropathy.Semantic proximity Read ↗

Production and characterization of transgenic mice harboring mutant human UMOD gene.Semantic proximity Read ↗

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