Evidence map›Paper›PMID 41631259›Full record

ArticleJIMD reports2026

Metabolic Stroke: Atypical Presentation of Succinic Semialdehyde Dehydrogenase Deficiency.

Sharmila Kiss, Richard J Leventer, Cormac Duff, Emma Macdonald-Laurs, Olivia-Paris Quinn, Fahaz Nazer, Michelle Cao, Abisha Srikumar, Jenzen Dalina, Mary Eggington and 1 more

Abstract read
In one paragraph

Article in JIMD reports, 2026. 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
–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

1 citing paper in PubMed.

  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

11 authors.

Sharmila KissDepartment of Metabolic Medicine The Royal Children's Hospital Parkville Victoria Australia.ORCID https://orcid.org/0000-0002-4664-0690
Richard J LeventerDepartment of Neurology The Royal Children's Hospital Parkville Victoria Australia.
Cormac DuffDepartment of Metabolic Medicine The Royal Children's Hospital Parkville Victoria Australia.ORCID https://orcid.org/0000-0003-1269-0558
Emma Macdonald-LaursDepartment of Neurology The Royal Children's Hospital Parkville Victoria Australia.ORCID https://orcid.org/0000-0002-9894-4610
Olivia-Paris QuinnDepartment of Neurology The Royal Children's Hospital Parkville Victoria Australia.
Fahaz NazerVictorian Clinical Genetics Services, Murdoch Children's Research Institute Parkville Victoria Australia.ORCID https://orcid.org/0000-0002-4134-3531
Michelle CaoVictorian Clinical Genetics Services, Murdoch Children's Research Institute Parkville Victoria Australia.ORCID https://orcid.org/0000-0001-8984-4880
Abisha SrikumarVictorian Clinical Genetics Services, Murdoch Children's Research Institute Parkville Victoria Australia.
Jenzen DalinaVictorian Clinical Genetics Services, Murdoch Children's Research Institute Parkville Victoria Australia.
Mary EggingtonVictorian Clinical Genetics Services, Murdoch Children's Research Institute Parkville Victoria Australia.
Joy Yaplito- LeeVictorian Clinical Genetics Services, Murdoch Children's Research Institute Parkville Victoria Australia.ORCID https://orcid.org/0000-0002-6158-6215

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Succinic semialdehyde dehydrogenase (SSADH) deficiency is a rare autosomal recessive neurometabolic disorder caused by biallelic pathogenic variants in

Identifiers

PMID41631259
PMCPMC12861592

What OpenQuestion holds

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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.