Evidence map›Paper›PMID 33659201›Full record

ArticleJournal of epilepsy research2020

Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment.

Piero Pavone, Xena Giada Pappalardo, Ugochi Ngaobiri Nelly Ohazuruike, Pasquale Striano, Pasquale Parisi, Giovanni Corsello, Simona Domenica Marino, Martino Ruggieri, Enrico Parano, Raffaele Falsaperla

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PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of epilepsy research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

10 authors at 6 institutions in 1 country.

Piero PavoneUnit of Pediatrics and Pediatric Emergency, University Hospital "Policlinico-Vittorio Emanuele", Catania, Italy.
Xena Giada PappalardoUnit of Catania, Institute for Biomedical Research and Innovation (IRIB), National Council of Research, Catania, Italy.
Ugochi Ngaobiri Nelly OhazuruikeDepartment of General Surgery and Medical-Surgical Specialties, University of Catania, Catania, Italy.
Pasquale StrianoPediatric Neurology and Muscular Diseases Unit, IRCCS 'G. Gaslini' Institute, Genoa, Italy.
Pasquale ParisiChild Neurology, NESMOS Department, Faculty of Medicine & Psychology, "Sapienza" University, c/o Sant'Andrea Hospital, Rome, Italy.
Giovanni CorselloDepartment of Sciences for Health Promotion and Mother and Child Care "G. D'Alessandro", University of Palermo, Palermo, Italy.
Simona Domenica MarinoUnit of Neonatology University Hospital "Policlinico-Vittorio Emanuele", Catania, Italy.
Martino RuggieriUnit of Pediatrics and Pediatric Emergency, University Hospital "Policlinico-Vittorio Emanuele", Catania, Italy.
Enrico ParanoUnit of Catania, Institute for Biomedical Research and Innovation (IRIB), National Council of Research, Catania, Italy.
Raffaele FalsaperlaUnit of Neonatology University Hospital "Policlinico-Vittorio Emanuele", Catania, Italy.
Azienda Ospedaliero-Universitaria Policlinico - Vittorio Emanuele · ITUniversity of Catania · ITAzienda Ospedaliera Sant'Andrea · ITInstitute for Biomedical Research and Innovation · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 15q13.3 microdeletion (microdel15q13.3) syndrome (OMIM 612001) has been reported in healthy subjects as well as in individuals with a wide spectrum of clinical manifestations ranging from mild to severe neurological disorders, including developmental delay/intellectual disability, autism spectrum disorder, schizophrenia, epilepsy, behavioral problems and speech dysfunction. This study explored the link between this genomic rearrangement and nocturnal frontal lobe epilepsy (NFLE), which could improve the clinical interpretation. A clinical and genomic investigation was carried out on an 8-year-girl with a

Indexed as

Chromosome breakpointsFrontal lobe epilepsyHypertrichosisLanguage disordersMigraine disorders

Identifiers

PMID33659201
PMCPMC7903043
OpenAlexW3127479353

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.