Evidence map›Paper›PMID 36830958›Full record

ArticleBiomedicines2023

A Century of Progress on Wilson Disease and the Enduring Challenges of Genetics, Diagnosis, and Treatment.

Louis C Penning, Marina Berenguer, Anna Czlonkowska, Kay L Double, Petr Dusek, Carmen Espinós, Svetlana Lutsenko, Valentina Medici, Wiebke Papenthin, Wolfgang Stremmel and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

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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

12 authors at 9 institutions in 7 countries.

Louis C PenningDepartment of Clinical Sciences of Companion Animals, Faculty of Veterinary Medicine, Utrecht University, 3584 CM Utrecht, The Netherlands.ORCID 0000-0002-0880-9475
Marina BerenguerDigestive Medicine Department, Ciberehd & IISLaFe, Hospital U. i P. La Fe, University of Valencia, 46010 Valenci, Spain.ORCID 0000-0001-9246-4264
Anna CzlonkowskaSecond Department of Neurology, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland.ORCID 0000-0002-1956-1866
Kay L DoubleBrain and Mind Centre and School of Medical Sciences (Neuroscience), The University of Sydney, Sydney, NSW 2006, Australia.
Petr DusekDepartment of Radiology, Charles University and General University Hospital, 128 08 Prague, Czech Republic.ORCID 0000-0003-4877-9642
Carmen EspinósRare Neurodegenerative Diseases Lab, Centro de Investigacion Principe Felipe, 46012 Valencia, Spain.ORCID 0000-0003-4435-1809
Svetlana LutsenkoDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 1800, USA.
Valentina MediciDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, University of California Davis, Sacramento, CA 59817, USA.ORCID 0000-0001-5438-284X
Wiebke PapenthinGerman Society for Wilson disease Patients (Morbus Wilson e.V.), Zehlendorfer Damm 119, D-14532 Kleinnachnow, Germany.
Wolfgang StremmelPrivate Practice for Internal Medicine, Beethovenstraße 2, D-76530 Baden-Baden, Germany.
Jose WillemseDutch Society for Liver Disease Patients (Nederlandse Leverpatienten Vereniging), 3828 NS Hoogland, The Netherlands.
Ralf WeiskirchenInstitute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry (IFMPEGKC), RWTH Aachen University Hospital Aachen, D-52074 Aachen, Germany.ORCID 0000-0003-3888-0931
Centro de Investigacion Principe Felipe · ESCharles University · CZInstitute of Psychiatry and Neurology · PLJohns Hopkins University · USThe University of Sydney · AUUniversitat de València · ESUniversitätsklinikum Aachen · DEUniversity of California, Davis · USUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wilson disease (WD) is a rare, inherited metabolic disorder manifested with varying clinical presentations including hepatic, neurological, psychiatric, and ophthalmological features, often in combination. Causative mutations in the

Indexed as

copper accumulationhepatic disfunctionneurological disfunctionpatients’ involvementpsychiatric disordersWilson disease

Identifiers

PMID36830958
PMCPMC9953205
OpenAlexW4318777149

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.