ArticleKidney international reports2026
Clinical and Genetic Insights Into Isolated Proteinuria With
Article in Kidney international reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- High prevalence of genetic variants in asymptomatic proteinuria detected via urine screening in 3-year-old children in Japan.Pediatric nephrology (Berlin, Germany) · 2026Article
- The Long and the Short of it: How Cubilin Isoforms are Affected by Genetic Variants.Kidney international reports · 2026Article
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Authors and funding
18 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Cubilin is a multiligand receptor essential for vitamin B12 uptake in the small intestine and for low-molecular-weight protein reabsorption in the proximal tubule. Biallelic Methods: We evaluated patients with proteinuria carrying biallelic Results: Fifty-two patients from 42 families were analyzed, and 40 Conclusion: Patients with biallelic
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Registered trials
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