Evidence map›Paper›PMID 37265023›Full record

ArticleBrain pathology (Zurich, Switzerland)2024

Distribution of ferritin complex in the adult brain and altered composition in neuroferritinopathy due to a novel variant in the ferritin heavy chain gene FTH1 (c.409_410del; p.H137Lfs*4).

Vincent Umathum, Axel Weber, Daniel Amsel, Ioannis Alexopoulos, Christina Becker, Angela Roth, Andreas Günther, Carmen Selignow, Nadja Ritschel, Anna Nishimura and 5 more

Abstract readLetter
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Introducing a novel variant in the FTH1 gene; A closer look at FTH1-related neuroferritinopathy as a neurodegeneration with brain iron accumulation (NBIA) disorder.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  2. Article
  3. Autosomal DominantNeurology. Genetics · 2026
    Article
  4. Review
  5. 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

15 authors.

Vincent UmathumInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.ORCID 0000-0002-6235-7908
Axel WeberInstitute of Human Genetics, Justus-Liebig-University Giessen, Giessen, Germany.
Daniel AmselInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.
Ioannis AlexopoulosInstitute for Lung Health, Justus-Liebig-University Giessen, Giessen, Germany.
Christina BeckerInstitute of Pathology, Cytology and Molecular Pathology, Wetzlar, Germany.
Angela RothInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.
Andreas GüntherDepartment of Pulmonology, Agaplesion Evangelisches Krankenhaus Giessen, Giessen, Germany.
Carmen SelignowInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.
Nadja RitschelInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.
Anna NishimuraInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.
Alexander SchaiterInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.
Attila NémethInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.
Peter F M van der VenInstitute for Cell Biology, University of Bonn, Bonn, Germany.ORCID 0000-0002-9750-8913
Till AckerInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.
Anne SchänzerInstitute of Neuropathology, Justus-Liebig-University Giessen, Giessen, Germany.ORCID 0000-0002-2014-2028

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ApoferritinsIron Metabolism DisordersAdultBrainFerritinsHumansNeuroaxonal DystrophiesOxidoreductasesApoferritinsFerritinsFTH1 protein, humanOxidoreductases

Identifiers

PMID37265023
PMCPMC10711253

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.