Evidence map›Paper›PMID 34295499›Full record

ArticleClinical case reports2021

An unusual presentation of Huntington's disease.

Martin Schulze Westhoff, Alma Osmanovic, Catharina Meissner, Johannes Heck, Nima Mahmoudi, Corinna Hendrich, Georg Berding, Johanna Seifert, Stefan Bleich, Helge Frieling and 2 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

12 authors at 1 institution in 1 country.

Martin Schulze WesthoffDepartment of Psychiatry Social Psychiatry and Psychotherapy Hannover Medical School Hannover Germany.ORCID https://orcid.org/0000-0003-3262-8137
Alma OsmanovicDepartment of Neurology Hannover Medical School Hannover Germany.ORCID https://orcid.org/0000-0002-6012-8423
Catharina MeissnerDepartment of Psychiatry Social Psychiatry and Psychotherapy Hannover Medical School Hannover Germany.ORCID https://orcid.org/0000-0002-8678-7419
Johannes HeckInstitute for Clinical Pharmacology Hannover Medical School Hannover Germany.ORCID https://orcid.org/0000-0002-5382-3014
Nima MahmoudiDepartment of Diagnostic and Interventional Neuroradiology Hannover Medical School Hannover Germany.
Corinna HendrichInstitute for Human Genetics Hannover Medical School Hannover Germany.
Georg BerdingDepartment of Nuclear Medicine Hannover Medical School Hannover Germany.ORCID https://orcid.org/0000-0001-5592-8373
Johanna SeifertDepartment of Psychiatry Social Psychiatry and Psychotherapy Hannover Medical School Hannover Germany.
Stefan BleichDepartment of Psychiatry Social Psychiatry and Psychotherapy Hannover Medical School Hannover Germany.ORCID https://orcid.org/0000-0001-5146-9720
Helge FrielingDepartment of Psychiatry Social Psychiatry and Psychotherapy Hannover Medical School Hannover Germany.ORCID https://orcid.org/0000-0002-6583-1433
Tillmann KrügerDepartment of Psychiatry Social Psychiatry and Psychotherapy Hannover Medical School Hannover Germany.
Adrian GrohDepartment of Psychiatry Social Psychiatry and Psychotherapy Hannover Medical School Hannover Germany.ORCID https://orcid.org/0000-0002-4407-3557
Medizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe the case of a 59-year-old woman who exhibited psychotic symptoms, cognitive dysfunction, and restlessness. While the clinical picture and 18F-FDG PET/CT suggested the presence of a tauopathy, especially frontotemporal dementia or progressive supranuclear palsy, genetic testing eventually revealed Huntington's disease.

Indexed as

18F‐FDG PET/CTfrontotemporal dementiaHuntington's diseasepsychosistauopathies

Identifiers

PMID34295499
PMCPMC8283861
OpenAlexW3186264795

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.