ReviewPediatric nephrology (Berlin, Germany)2005
Familial hematurias: what we know and what we don't.
Review in Pediatric nephrology (Berlin, Germany), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 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
12 citing papers in PubMed, 42 citations in OpenAlex.
- Hidden genetics behind glomerular scars: an opportunity to understand the heterogeneity of focal segmental glomerulosclerosis?Pediatric nephrology (Berlin, Germany) · 2024Review
- COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?BMC nephrology · 2018Article
- Article
- Article
- The role of molecular genetics in diagnosing familial hematuria(s).Pediatric nephrology (Berlin, Germany) · 2012Review
- Evidence that NPHS2-R229Q predisposes to proteinuria and renal failure in familial hematuria.Pediatric nephrology (Berlin, Germany) · 2012Article
- Deletion of von Hippel-Lindau in glomerular podocytes results in glomerular basement membrane thickening, ectopic subepithelial deposition of collagen {alpha}1{alpha}2{alpha}1(IV), expression of neuroglobin, and proteinuria.The American journal of pathology · 2010Article
- Familial hematuria.Pediatric nephrology (Berlin, Germany) · 2009Review
- Thin basement membrane nephropathy: is there genetic predisposition to more severe disease?Pediatric nephrology (Berlin, Germany) · 2009Article
- Development of kidney glomerular endothelial cells and their role in basement membrane assembly.Organogenesis · 2009Article
- Persistent haematuria and proteinuria due to glomerular disease in related Abyssinian cats.Journal of feline medicine and surgery · 2008Article
- "Treasure your exceptions": recent advances in molecular genetics of glomerular disease.Journal of applied genetics · 2008Review
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
Over the past 30 years we have learned a great deal about the molecular genetics and natural history of familial forms of hematuria. Our enhanced understanding of these conditions has yet to generate effective therapies for Alport syndrome, the form of familial hematuria associated with end-stage renal disease. This review briefly presents the current state of knowledge about familial hematuria and argues for the organization of clinical therapeutic trials in Alport syndrome.
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.