Evidence map›Paper›PMID 37201161›Full record

ArticleCase reports in nephrology and dialysis

Unusual Cause of Thrombocytopenia and Renal Failure in a 14-Year-Old Boy (MYH9-Associated Disorders).

Karol Granak, Miroslava Brndiarova, Matej Vnucak, Ivana Plamenova, Regina Behulova Lohajova, Romana Valencikova, Milos Jesenak, Ivana Dedinska

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports in nephrology and dialysis. 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
0.6field-weighted citation impact, top 29% of its field
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, 2 citations in OpenAlex.

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 at 3 institutions in 1 country.

Karol GranakTransplant Center, University Hospital, Martin, Slovakia.
Miroslava BrndiarovaClinic of Children and Adolescents, Jessenius Faculty of Medicine and University Hospital, Comenius University in Bratislava, Martin, Slovakia.
Matej VnucakTransplant Center, University Hospital, Martin, Slovakia.
Ivana PlamenovaDepartment of Hematology and transfusiology, Jessenius Faculty of Medicine and University Hospital, Comenius University in Bratislava, Martin, Slovakia.
Regina Behulova LohajovaDepartment of Clinical Genetics, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
Romana ValencikovaDepartment of Clinical Genetics, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
Milos JesenakClinic of Children and Adolescents, Jessenius Faculty of Medicine and University Hospital, Comenius University in Bratislava, Martin, Slovakia.
Ivana DedinskaTransplant Center, University Hospital, Martin, Slovakia.
Martin University Hospital · SKComenius University Bratislava · SKVysoká Škola Zdravotníctva a Sociálnej Práce sv. Alžbety · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MYH9-associated disorders represent rare group of autosomal dominant diseases and are caused by pathogenic mutations in the

Indexed as

Macro-platelet-thrombocytopeniaMYH9-associated disordersNephropathy

Identifiers

PMID37201161
PMCPMC10186230
OpenAlexW4377093044

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.