Evidence map›Paper›PMID 33799813›Full record

ArticleGenes2021

Screening for Plasminogen Mutations in Hereditary Angioedema Patients.

Henriette Farkas, Anna Dóczy, Edina Szabó, Lilian Varga, Dorottya Csuka

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

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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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

5 authors at 1 institution in 1 country.

Henriette FarkasHungarian Angioedema Center of Reference and Excellence, Department of Internal Medicine and Haematology, Semmelweis University, H-1088 Budapest, Hungary.
Anna DóczyHeart and Vascular Center, Semmelweis University, H-1122 Budapest, Hungary.
Edina SzabóMTA-SE Research Group of Immunology and Haematology, Research Laboratory, Department of Internal Medicine and Haematology, Hungarian Academy of Sciences and Semmelweis University, H-1088 Budapest, Hungary.
Lilian VargaHungarian Angioedema Center of Reference and Excellence, Department of Internal Medicine and Haematology, Semmelweis University, H-1088 Budapest, Hungary.
Dorottya CsukaHungarian Angioedema Center of Reference and Excellence, Department of Internal Medicine and Haematology, Semmelweis University, H-1088 Budapest, Hungary.ORCID 0000-0003-3610-9852
Semmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary angioedema (HAE) is a rare disease belonging to the group of bradykinin-mediated angioedemas, characterized by recurring edematous episodes involving the subcutaneous and/or submucosal tissues. Most cases of HAE are caused by mutations in the

Indexed as

MutationAngioedemas, HereditaryAngiopoietin-1Complement C1 Inhibitor ProteinFactor XIIFemaleHumansKininogensMalePlasminogenSulfotransferasesAngiopoietin-1ANGPT1 protein, humanComplement C1 Inhibitor ProteinFactor XIIKininogensKNG1 protein, humanPlasminogenSERPING1 protein, humanSulfotransferasesbiorepositoryfamily screeninghereditary angioedemamutationplasminogen

Identifiers

PMID33799813
PMCPMC7998782
OpenAlexW3134333522

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.