Evidence map›Paper›PMID 30805006›Full record

ArticleCase reports in medicine2019

Dravet Syndrome in Lebanon: First Report on Cases with

Saada Alame, Eliane El-Houwayek, Caroline Nava, Sandra Sabbagh, Ali Fawaz, Anne-Celine Gillart, Dana Hasbini, Christel Depienne, André Mégarbané

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

Article in Case reports in medicine, 2019. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Dravet Syndrome: A Rare Form of Epilepsy.Case reports in medicine · 2024
    Article
  3. Cohort of Phenotype, Genotype, and Outcome ofJournal of pediatric genetics · 2023
    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

9 authors.

Saada Alame *Neuropediatrics Department, Lebanese University, Beirut, Lebanon.
Eliane El-Houwayek *Pediatrics, Lebanese University, Beirut, Lebanon.
Caroline NavaInserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière (ICM), F-75013 Paris, France.
Sandra SabbaghService de Pediatrie, Hotel-Dieu de France, Beirut, Lebanon.
Ali FawazNeuropediatrics Department, Lebanese University, Beirut, Lebanon.
Anne-Celine GillartInstitut Jérôme Lejeune, Paris, France.
Dana HasbiniNeuropediatrics Department, Rafic Hariri University Hospital, Beirut, Lebanon.
Christel DepienneInserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière (ICM), F-75013 Paris, France.
André MégarbanéInstitut Jérôme Lejeune, Paris, France.ORCID 0000-0003-0714-2469

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dravet syndrome, also known as severe myoclonic epilepsy in infancy, is a rare disease characterized by the appearance of different types of seizures in a healthy baby, triggered by various factors and stressful events. We report 8 Lebanese cases referred for molecular analysis of the

Identifiers

PMID30805006
PMCPMC6360541

What OpenQuestion holds

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Registered trials

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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.