Evidence map›Paper›PMID 29134474›Full record

ArticleStem cell reviews and reports2018

Familial Limbal Stem Cell Deficiency: Clinical, Cytological and Genetic Characterization.

Lubica Dudakova, Sek-Shir Cheong, Stanislava Reinstein Merjava, Pavlina Skalicka, Marcela Michalickova, Michalis Palos, Gabriela Mahelkova, Deli Krizova, Martin Hlozanek, Marie Trkova and 10 more

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Stem cell reviews and reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

20 authors.

Lubica DudakovaResearch Unit for Rare Diseases; Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 2, Praha 2, 128 08, Prague, Czech Republic.
Sek-Shir CheongUCL Institute of Ophthalmology, London, UK.
Stanislava Reinstein MerjavaResearch Unit for Rare Diseases; Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 2, Praha 2, 128 08, Prague, Czech Republic.
Pavlina SkalickaResearch Unit for Rare Diseases; Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 2, Praha 2, 128 08, Prague, Czech Republic.
Marcela MichalickovaDepartment of Ophthalmology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Michalis PalosDepartment of Ophthalmology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Gabriela MahelkovaDepartment of Ophthalmology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Deli KrizovaOphthalmology Department, Third Faculty of Medicine, Charles University and Teaching Hospital Kralovske Vinohrady, Prague, Czech Republic.
Martin HlozanekDepartment of Ophthalmology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Marie TrkovaGENNET, Prague, Czech Republic.
Jena L ChojnowskiDepartment of Cellular Biology, University of Georgia, Athens, GA, 30602, USA.
Enkela HrdlickovaDepartment of Ophthalmology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Nikolas PontikosUCL Genetics Institute, London, UK.
Vincent PlagnolUCL Genetics Institute, London, UK.
Viera VeseláResearch Unit for Rare Diseases; Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 2, Praha 2, 128 08, Prague, Czech Republic.
Katerina JirsovaResearch Unit for Rare Diseases; Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 2, Praha 2, 128 08, Prague, Czech Republic.
Alison J HardcastleUCL Institute of Ophthalmology, London, UK.
Martin FilipecEuropean Eye Clinic Lexum, Prague, Czech Republic.
James D LauderdaleDepartment of Cellular Biology, University of Georgia, Athens, GA, 30602, USA.
Petra LiskovaResearch Unit for Rare Diseases; Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 2, Praha 2, 128 08, Prague, Czech Republic. petra.liskova@lf1.cuni.cz.ORCID 0000-0001-7834-8486

Funding

Grantová Agentura, Univerzita Karlova 227015/2017Univerzita Karlova v Praze PROGRES-Q26/LF1Univerzita Karlova v Praze SVV 260367/2017Univerzita Karlova v Praze UNCE 204011
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Corneal DiseasesEpithelium, CornealFemaleHumansLimbus CorneaeMaleStem Cells

Identifiers

PMID29134474

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.