Evidence map›Paper›PMID 41230709›Full record

ArticleMovement disorders clinical practice2026

Huntington's Disease-like Syndrome as a Rare Presentation of CACNA1A-Related Disorder.

Petros Boumis, Constantin Potagas, Christos Koros, Vasilios Constantinides, Nikolaos Ragazos, Chrysoula Koniari, Stavroula Aristeidou, Chrisoula Kartanou, Emmanouela Linardaki, Nektarios Tavernarakis and 5 more

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

Article in Movement disorders clinical practice, 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

15 authors.

Petros Boumis1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Constantin Potagas1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Christos Koros1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.ORCID https://orcid.org/0000-0001-5806-0717
Vasilios Constantinides1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.ORCID https://orcid.org/0000-0001-7432-5009
Nikolaos RagazosNeurogenetics Unit, 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian Universtiy of Athens, Athens, Greece.
Chrysoula KoniariNeurogenetics Unit, 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian Universtiy of Athens, Athens, Greece.
Stavroula AristeidouNeurogenetics Unit, 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian Universtiy of Athens, Athens, Greece.
Chrisoula KartanouNeurogenetics Unit, 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian Universtiy of Athens, Athens, Greece.
Emmanouela LinardakiInstitute of Molecular Biology and Biotechnology (IMBB), Foundation for Research and Technology-Hellas (FORTH), Heraklion, Greece.
Nektarios TavernarakisInstitute of Molecular Biology and Biotechnology (IMBB), Foundation for Research and Technology-Hellas (FORTH), Heraklion, Greece.ORCID https://orcid.org/0000-0002-5253-1466
Evangelos Anagnostou1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Leonidas Stefanis1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.ORCID https://orcid.org/0000-0003-3569-8990
Socratis Papageorgiou1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Georgia KaradimaNeurogenetics Unit, 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian Universtiy of Athens, Athens, Greece.
Georgios KoutsisNeurogenetics Unit, 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian Universtiy of Athens, Athens, Greece.ORCID https://orcid.org/0000-0002-8980-8377

Funding

General Secretariat of Research and Innovation E01300001
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ataxiaCACNA1Achoreadystoniaepisodic ataxia type 2HD‐like syndromeHD phenocopyHuntington's disease

Identifiers

PMID41230709
PMCPMC13274665

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.