Evidence map›Paper›PMID 34450229›Full record

ArticleNeuroscience letters2021

The GM2 gangliosidoses: Unlocking the mysteries of pathogenesis and treatment.

Camilo Toro, Mosufa Zainab, Cynthia J Tifft

Abstract read
In one paragraph

Article in Neuroscience letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

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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

3 authors.

Camilo ToroNIH Undiagnosed Diseases Program, NIH Common Fund, National Institutes of Health, Bethesda MD, United States.
Mosufa ZainabGlycosphingolipid Disorders Unit, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD, United States.
Cynthia J TifftNIH Undiagnosed Diseases Program, NIH Common Fund, National Institutes of Health, Bethesda MD, United States; Glycosphingolipid Disorders Unit, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD, United States.

Funding

Intramural NIH HHS Z99 HG999999
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Age of OnsetAnimalsbeta-Hexosaminidase alpha Chainbeta-Hexosaminidase beta ChainCerebellumDisease Models, AnimalEnzyme Replacement TherapyGangliosidoses, GM2Genetic TherapyGlucosyltransferasesGlycoside Hydrolase InhibitorsG(M2) GangliosideGray MatterHumansMutationRetinabeta-Hexosaminidase alpha Chainbeta-Hexosaminidase beta Chainceramide glucosyltransferaseGlucosyltransferasesGlycoside Hydrolase InhibitorsG(M2) GangliosideHEXA protein, humanHEXB protein, humanGangliosidosesGene therapyGM2HEXAHEXBHexosaminidase ALysosomal storage diseasesSandhoff diseaseTay-Sachs disease

Identifiers

PMID34450229
PMCPMC8572160

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.