Evidence map›Paper›PMID 36578597›Full record

ArticleProceedings (Baylor University. Medical Center)2023

A family case series of inherited thrombocytopenia.

Artur Borkowski, Jakub Gawryś, Gracjan Iwanek, Jarosław Dybko

Abstract readCase Reports
In one paragraph

Article in Proceedings (Baylor University. Medical Center), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. The Differential Diagnosis of Thromobocytopenia.Deutsches Arzteblatt international · 2025
    Review
  2. Article
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

4 authors.

Artur BorkowskiUniversity Clinical Hospital, Wroclaw, Poland.ORCID https://orcid.org/0000-0002-1019-8976
Jakub GawryśDepartment of Internal Medicine, Hypertension and Clinical Oncology, Faculty of Medicine, Wroclaw Medical University, Wroclaw, Poland.ORCID https://orcid.org/0000-0003-4520-3496
Gracjan IwanekUniversity Clinical Hospital, Wroclaw, Poland.
Jarosław DybkoDepartment of Hematology and Cellular Transplantation, Lower Silesian Center of Oncology, Wrocław, Poland.ORCID https://orcid.org/0000-0003-3555-2887

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited thrombocytopenia (IT) is a heterogeneous group of diseases with a genetic origin. The primary symptom presented by patients is a reduced platelet count in the peripheral blood. Nevertheless, certain forms of IT are characterized by the occurrence of other congenital malformations or predisposition to acquire additional diseases. Five related subjects with lifelong thrombocytopenia were admitted to our clinic. A total of 16 cases of persistent thrombocytopenia were investigated in the family history. Molecular and cytogenetic analysis covered

Indexed as

Gene mutationsinherited thrombocytopeniaplatelet countplatelets

Identifiers

PMID36578597
PMCPMC9762738

What OpenQuestion holds

Textmetadata
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.