Evidence map›Paper›PMID 37662840›Full record

ArticleFrontiers in genetics2023

Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors.

Viola Bianca Serio, Maria Palmieri, Simona Innamorato, Lorenzo Loberti, Chiara Fallerini, Francesca Ariani, Enrica Antolini, Jasmine Covarelli, Massimo Vaghi, Elisa Frullanti and 2 more

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

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. KRIT1 in vascular biology and beyond.Bioscience reports · 2024
    Review
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

12 authors at 3 institutions in 1 country.

Viola Bianca SerioMedical Genetics, University of Siena, Siena, Italy.
Maria PalmieriDepartment of Medical Biotechnologies, Med Biotech Hub and Competence Centre, University of Siena, Siena, Italy.
Simona InnamoratoMedical Genetics, University of Siena, Siena, Italy.
Lorenzo LobertiMedical Genetics, University of Siena, Siena, Italy.
Chiara FalleriniMedical Genetics, University of Siena, Siena, Italy.
Francesca ArianiMedical Genetics, University of Siena, Siena, Italy.
Enrica AntoliniMedical Genetics, University of Siena, Siena, Italy.
Jasmine CovarelliMedical Genetics, University of Siena, Siena, Italy.
Massimo VaghiRadiologia Interventistica, Ospedale Maggiore di Crema, Crema, Italy.
Elisa FrullantiDepartment of Medical Biotechnologies, Med Biotech Hub and Competence Centre, University of Siena, Siena, Italy.
Alessandra RenieriMedical Genetics, University of Siena, Siena, Italy.
Anna Maria PintoGenetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
University of Siena · ITAzienda Ospedaliera Universitaria Senese · ITAzienda Ospedaliera Ospedale Maggiore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a case of Klippel Trenaunay Syndrome that was monitored both clinically and molecularly over a period of 9 years. A somatic mosaic mutation of

Indexed as

case reportKlippel-Trenaunay SyndromeNGS-liquid biopsysquamous cell carcinoma adenocarcinomatailored therapy

Identifiers

PMID37662840
PMCPMC10469863
OpenAlexW4385984340

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.