Evidence map›Paper›PMID 32549268›Full record

ArticleBrain sciences2020

Familial Hemiplegic Migraine with an ATP1A4 Mutation: Clinical Spectrum and Carbamazepine Efficacy.

Giangennaro Coppola, Grazia Maria Giovanna Pastorino, Luigi Vetri, Floriana D'Onofrio, Francesca Felicia Operto

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Brain sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Genetics of migraine: where are we now?The journal of headache and pain · 2023
    Review
  3. Article
  4. Review
  5. Article
  6. The childhood migraine syndrome.Nature reviews. Neurology · 2021
    Review
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

5 authors at 2 institutions in 1 country.

Giangennaro CoppolaClinic of Child and Adolescent Neuropsychiatry, Department of Medicine, Surgery and Dentistry, Medical School University of Salerno, 84100 Salerno, Italy.ORCID 0000-0002-9574-0081
Grazia Maria Giovanna PastorinoClinic of Child and Adolescent Neuropsychiatry, Department of Medicine, Surgery and Dentistry, Medical School University of Salerno, 84100 Salerno, Italy.ORCID 0000-0003-0404-5495
Luigi VetriDepartment of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties (PROMISE), University of Palermo, 90133 Palermo, Italy.ORCID 0000-0002-0121-3396
Floriana D'OnofrioClinic of Child and Adolescent Neuropsychiatry, Department of Medicine, Surgery and Dentistry, Medical School University of Salerno, 84100 Salerno, Italy.ORCID 0000-0001-7498-0046
Francesca Felicia OpertoClinic of Child and Adolescent Neuropsychiatry, Department of Medicine, Surgery and Dentistry, Medical School University of Salerno, 84100 Salerno, Italy.ORCID 0000-0002-2444-8761
University of Salerno · ITUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An Italian family with familial hemiplegic migraine (FHM) with the absence of mutations in the known genes associated with this disorder, namely

Indexed as

ATP1A4 genecarbamazepineclinical symptomsfamilial hemiplegic migraine

Identifiers

PMID32549268
PMCPMC7349335
OpenAlexW3034651270

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.