Evidence map›Paper›PMID 39906419›Full record

ArticleCureus2025

ERCC6L2-Associated Inherited Bone Marrow Failure Syndrome: A Croatian Experience.

Izabela Kranjcec, Nusa Matijasic Stjepovic, Katarina Vulin, Maja Pavlovic, Toni Matic, Roberta Sarkanji-Golub, Gordana Jakovljevic, Jelena Roganovic

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PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 2025. 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

8 authors.

Izabela KranjcecDepartment of Oncology and Hematology, Children's Hospital Zagreb, Zagreb, HRV.
Nusa Matijasic StjepovicDepartment of Oncology and Hematology, Children's Hospital Zagreb, Zagreb, HRV.
Katarina VulinDepartment of Medical Genetics and Reproductive Health, Children's Hospital Zagreb, Zagreb, HRV.
Maja PavlovicDepartment of Oncology and Hematology, Children's Hospital Zagreb, Zagreb, HRV.
Toni MaticDepartment of Pediatrics, University Hospital Centre Zagreb, Zagreb, HRV.
Roberta Sarkanji-GolubDepartment of Medical and Laboratory Genetics, Endocrinology and Diabetology, Cytology Unit, Children's Hospital Zagreb, Zagreb, HRV.
Gordana JakovljevicDepartment of Oncology and Hematology, Children's Hospital Zagreb, Zagreb, HRV.
Jelena RoganovicDepartment of Oncology and Hematology, Children's Hospital Zagreb, Zagreb, HRV.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited bone marrow failure syndromes (IBMFS) are often misdiagnosed or lately diagnosed despite thorough medical assessment. Genomic investigations have largely facilitated correct diagnosis and enabled effective management in children with IBMFS. We present two unrelated adolescent females with unexplained prolonged bicytopenia, unremarkable medical history and normal physical findings who were diagnosed with a rare non-classical

Indexed as

bone marrow failure syndromegenetic testinghematopoetic myelodysplasialeukopeniathrombocytopenia

Identifiers

PMID39906419
PMCPMC11793847

What OpenQuestion holds

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Registered trials

None linked

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.