Evidence map›Paper›PMID 31942421›Full record

ArticleBalkan journal of medical genetics : BJMG2019

Infantile Alexander Disease with Late Onset Infantile Spasms and Hypsarrhythmia.

J Paprocka, B Rzepka-Migut, N Rzepka, A Jezela-Stanek, E Morava

Open access · goldAbstract read
In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. 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

5 authors at 2 institutions in 2 countries.

J PaprockaDepartment of Paediatric Neurology, School of Medicine, Medical University of Silesia, Katowice, Poland.
B Rzepka-MigutDepartment of Paediatric Neurology, St. Queen Jadwiga's Regional Clinical Hospital, No. 2, Rzeszów, Poland.
N RzepkaDepartment of Paediatric Neurology, St. Queen Jadwiga's Regional Clinical Hospital, No. 2, Rzeszów, Poland.
A Jezela-StanekDepartment of Genetics and Clinical Immunology, National Institute of Tuberculosis and Lung Diseases, Warsaw, Poland.
E MoravaHayward Genetics Center, Tulane University School of Medicine, New Orleans, LA, USA.
Medical University of Silesia · PLTulane University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alexander disease (AxD) is a rare autosomal dominant leukodystrophy with three clinical subtypes: infantile, juvenile and adult. Forms differ by age of symptoms occurrence and the clinical presentation. Although recent data suggest considering only two subtypes: type I (infantile onset with lesions extending to the cerebral hemispheres); type II (adult onset with primary involvement of subtentorial structures). Dominant mutations in the glial fibrillary acidic protein (

Indexed as

Alexander disease (AxD)ChildrenMacrocephaly

Identifiers

PMID31942421
PMCPMC6956636
OpenAlexW2997205411

What OpenQuestion 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 OpenQuestion graph.