Evidence map›Paper›PMID 33499149›Full record

ArticleInternational journal of molecular sciences2021

Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel

Maja Potrč, Marija Volk, Matteo de Rosa, Jože Pižem, Nataša Teran, Helena Jaklič, Aleš Maver, Brigita Drnovšek-Olup, Michela Bollati, Katarina Vogelnik and 6 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. A molecular perspective of gelsolin amyloidosis: An old foe with new faces.Cellular and molecular life sciences : CMLS · 2026
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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

16 authors at 3 institutions in 2 countries.

Maja PotrčEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Marija VolkClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0003-2807-6114
Matteo de RosaInstitute of Biophysics, National Research Council, 20133 Milano, Italy.ORCID 0000-0002-8634-5426
Jože PižemInstitute of Pathology, Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.
Nataša TeranClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Helena JakličClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Aleš MaverClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Brigita Drnovšek-OlupEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Michela BollatiInstitute of Biophysics, National Research Council, 20133 Milano, Italy.
Katarina VogelnikDepartment of Neurology, University of Ljubljana, 1000 Ljubljana, Slovenia.
Alojzija HočevarDepartment of Rheumatology, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0002-7361-6549
Ana GornikEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Vladimir PfeiferEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Borut PeterlinClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Marko HawlinaEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Ana FakinEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0001-6132-4808
Ljubljana University Medical Centre · SIUniversity of Ljubljana · SIUniversity of Milan · IT

Funding

Javna Agencija za Raziskovalno Dejavnost RS J3-1750
6 · The paper itself

Abstract

Gelsolin amyloidosis typically presents with corneal lattice dystrophy and is most frequently associated with pathogenic

Indexed as

MutationAdultAgedAmyloid Neuropathies, FamilialAmyloidosisAmyloidosis, FamilialCorneal DiseasesCorneal Dystrophies, HereditaryExomeFamily HealthFemaleFundus OculiGelsolinGenetic Association StudiesGlutamic AcidHumansGelsolinGlutamic AcidLysinecutis laxagelsolin amyloidosisGSNheart arrhythmialattice corneal dystrophyMeretoja syndromeoptical coherence tomographyoptic neuropathy

Identifiers

PMID33499149
PMCPMC7865823
OpenAlexW3123766461

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.