ReviewPediatric nephrology (Berlin, Germany)2013
How benign is hematuria? Using genetics to predict prognosis.
Review in Pediatric nephrology (Berlin, Germany), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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
13 citing papers in PubMed, 38 citations in OpenAlex.
- NovelWorld journal of clinical cases · 2023Article
- Identification ofFrontiers in genetics · 2022Article
- Tale of two nephropathies; co-occurring Alport syndrome and IgA nephropathy, a case report.BMC nephrology · 2021Article
- Co-existence of Alport syndrome and C3 glomerulonephritis in a proband with family history.European journal of medical research · 2021Article
- Raising the Volume on Alport Syndrome: A Patient Perspective.Kidney360 · 2020Article
- Genetic mutational testing of Chinese children with familial hematuria with biopsy‑proven FSGS.Molecular medicine reports · 2018Article
- A novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagen.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2016Article
- Prevalence of hypertension, obesity, hematuria and proteinuria amongst healthy adolescents living in Western Saudi Arabia.Saudi medical journal · 2016Article
- Isolated microscopic haematuria of glomerular origin: clinical significance and diagnosis in the 21st century.Clinical medicine (London, England) · 2015Article
- Pathogenesis of glomerular haematuria.World journal of nephrology · 2015Review
- Observational
- Genetic testing can resolve diagnostic confusion in Alport syndrome.Clinical kidney journal · 2014Article
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author at 1 institution in 1 country.
Funding
Abstract
Hematuria is a common presenting feature of glomerular disease and is sometimes associated with kidney failure later in life. Where isolated microscopic hematuria occurs in children and young adults, an underlying monogenic disorder, such as Alport syndrome or thin basement membrane nephropathy, is frequently responsible. In this review, these and other diseases, which often present with isolated microscopic hematuria, including hereditary angiopathy, nephropathy, aneurysms, and muscle cramps (HANAC) syndrome, IgA nephropathy, and CFHR5 nephropathy, are discussed together with the associated molecular pathology, clinical features, and prognosis. Genetic testing for these conditions used in clinical practice can provide important diagnostic and prognostic information that is relevant to the patient and their family, particularly when kidney transplantation is considered.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.