Evidence map›Paper›PMID 41870659›Full record

ArticleJournal of neurology2026

Clinical and genetic diagnostic challenges in presumed hereditary ataxia.

Helene Faust, Patricia Duffek, Stephan Drukewitz, Janina Gburek-Augustat, Petra Baum, Christa-Caroline Bergner, Steffen Syrbe, Julian Schröter, Rami Abou Jamra, Denny Popp

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Helene FaustInstitute of Human Genetics, University Hospital Schleswig-Holstein, Arnold-Heller-Str. 3, 24105, Kiel, Germany. helene.faust@uksh.de.ORCID http://orcid.org/0009-0005-2853-341X
Patricia DuffekInstitute of Human Genetics, University Medical Center Leipzig, Philipp-Rosenthal-Str. 55, 04103, Leipzig, Germany.
Stephan DrukewitzInstitute of Human Genetics, University Medical Center Leipzig, Philipp-Rosenthal-Str. 55, 04103, Leipzig, Germany.
Janina Gburek-AugustatDivision of Neuropediatrics, Hospital for Children and Adolescents, University Hospital Leipzig, Leipzig, Germany.
Petra BaumDepartment of Neurology, University Hospital Leipzig, Leipzig, Germany.
Christa-Caroline BergnerDepartment of Neurology, University Hospital Leipzig, Leipzig, Germany.
Steffen SyrbeDivision of Pediatric Epileptology, Clinic 1, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Heidelberg University, Heidelberg, Germany.
Julian SchröterDivision of Pediatric Epileptology, Clinic 1, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Heidelberg University, Heidelberg, Germany.
Rami Abou JamraInstitute of Human Genetics, University Medical Center Leipzig, Philipp-Rosenthal-Str. 55, 04103, Leipzig, Germany.
Denny PoppInstitute of Human Genetics, University Medical Center Leipzig, Philipp-Rosenthal-Str. 55, 04103, Leipzig, Germany. denny.popp@medizin.uni-leipzig.de.ORCID http://orcid.org/0000-0001-5656-2027

Funding

Medizinische Fakultät, Universität Leipzig 965000-029
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID41870659
PMCPMC13009057

What OpenQuestion holds

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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.