Evidence map›Paper›PMID 42877346›Full record

ArticleBalkan journal of medical genetics : BJMG2026

Long-Term Kidney and Patient Survival after Deceased Donor Transplantation in Two Brothers with Alport Syndrome from the Same Donor.

G Severova, I Hamamdzieva, P Dzekova-Vidimliski, L Trajceska, I Rambabova-Bushljetik, N Gjorgjievski, A Trifunovski, O Ivanovski, V Tasic

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In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

G SeverovaUniversity Clinic of Nephrology, Skopje, Republic of North Macedonia.
I HamamdzievaUniversity Clinic of Nephrology, Skopje, Republic of North Macedonia.
P Dzekova-VidimliskiUniversity Clinic of Nephrology, Skopje, Republic of North Macedonia.
L TrajceskaUniversity Clinic of Nephrology, Skopje, Republic of North Macedonia.
I Rambabova-BushljetikUniversity Clinic of Nephrology, Skopje, Republic of North Macedonia.
N GjorgjievskiUniversity Clinic of Nephrology, Skopje, Republic of North Macedonia.
A TrifunovskiUniversity Clinic of Urology, Skopje, Republic of North Macedonia.
O IvanovskiUniversity Clinic of Urology, Skopje, Republic of North Macedonia.
V TasicUniversity Pediatric Clinic, Skopje, Republic of North Macedonia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alport syndrome is a hereditary disorder caused by a mutation in type IV collagen, leading to progressive kidney disease and eventual end- stage renal failure. Kidney transplantation represents the optimal therapeutic option, typically associated with excellent graft survival. We report a long-term outcome in two brothers with genetically confirmed Alport syndrome (

Indexed as

Alport syndromeend–stage kidney diseasekidney transplantation

Identifiers

PMID42877346
PMCPMC13667935

What OpenQuestion holds

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Registered trials

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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.