Evidence map›Paper›PMID 41551069›Full record

ArticleClinical parkinsonism & related disorders2026

Confirmation of biallelic

Arnaud Storck, Marie Thérèse Abiwarde, Gaelle Hardy, Anne-Sophie Lebre, Sophie Scheidecker, Maria Cristina Antal, Mathieu Anheim, Thomas Wirth

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical parkinsonism & related disorders, 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

8 authors.

Arnaud StorckService de Neurologie, Département de Neurologie, Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, 1, Avenue Molière, Strasbourg, Cedex, France.
Marie Thérèse AbiwardeService de Neurologie Pédiatrique, Hôpital Universitaire de Strasbourg, Strasbourg, France.
Gaelle HardyUM de Génétique Moléculaire : Maladies Héréditaires et Oncologie, Institut de Biologie et de Pathologie, CHU Grenoble Alpes, Grenoble, France.
Anne-Sophie LebreUniversité Paris Cité, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, [Krebs team], 75014 Paris, France.
Sophie ScheideckerLaboratories of Genetic Diagnosis, Institut de Génétique Médicale d'Alsace (IGMA), Strasbourg University Hospitals Strasbourg France, Strasbourg, France.
Maria Cristina AntalUniversité de Strasbourg - Faculté de Médecine, Maïeutique et Sciences pour la Santé Institut d'Histologie - Service Central de Microscopie Électronique, ICube UMR7357 - équipe IMIS Hôpitaux Universitaires - Service de Pathologie - UF6349 Foetopathologie, France.
Mathieu AnheimService de Neurologie, Département de Neurologie, Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, 1, Avenue Molière, Strasbourg, Cedex, France.
Thomas WirthService de Neurologie, Département de Neurologie, Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, 1, Avenue Molière, Strasbourg, Cedex, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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Indexed as

DystoniaEndolysosomial pathwayNeurogeneticSpastic paraplegia

Identifiers

PMID41551069
PMCPMC12808586

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.