Evidence map›Paper›PMID 42741518›Full record

ArticleJIMD reports2026

Asparagine Synthetase Deficiency: Neuropathological Evidence of Disrupted Cortical Development.

Mihaela Bobić, Goran Sedmak, Ema Bokulić, Tila Medenica, Tamara Žigman, Bernarda Medlobi Vinković, Viktorija Antolović, Nenad Kešin, Ivan Lehman, Ana Škaričić and 6 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. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Mihaela BobićCroatian Institute for Brain Research University of Zagreb, School of Medicine Zagreb Croatia.ORCID https://orcid.org/0000-0002-1588-7658
Goran SedmakCroatian Institute for Brain Research University of Zagreb, School of Medicine Zagreb Croatia.
Ema BokulićCroatian Institute for Brain Research University of Zagreb, School of Medicine Zagreb Croatia.ORCID https://orcid.org/0000-0002-5732-7560
Tila MedenicaCroatian Institute for Brain Research University of Zagreb, School of Medicine Zagreb Croatia.ORCID https://orcid.org/0000-0002-4529-6728
Tamara ŽigmanDepartment of Pediatrics University Hospital Centre Zagreb Zagreb Croatia.ORCID https://orcid.org/0000-0003-1184-8798
Bernarda Medlobi VinkovićNeonatology Unit County Hospital Čakovec Čakovec Croatia.
Viktorija AntolovićSpecial Hospital for Chronic Diseases in Children Gornja Bistra Croatia.
Nenad KešinSpecial Hospital for Chronic Diseases in Children Gornja Bistra Croatia.
Ivan LehmanDepartment of Pediatrics University Hospital Centre Zagreb Zagreb Croatia.ORCID https://orcid.org/0009-0003-5088-0659
Ana ŠkaričićDepartment of Laboratory Diagnostics University Hospital Centre Zagreb Zagreb Croatia.
Mirjana NovoselecDepartment of Diagnostic and Interventional Neuroradiology University Hospital Centre Zagreb Zagreb Croatia.
Josipa MateševacDepartment for Functional Genomics, Centre for Translational and Clinical Research University Hospital Centre Zagreb Zagreb Croatia.
Monica Kirigin KalamarClinical Department of Pathology and Cytology "Ljudevit Jurak" University Hospital Center "Sestre Milosrdnice" Zagreb Croatia.
Sanda Huljev FrkovićDepartment of Pediatrics University Hospital Centre Zagreb Zagreb Croatia.ORCID https://orcid.org/0000-0003-1513-2965
Ivo BarićDepartment of Pediatrics University Hospital Centre Zagreb Zagreb Croatia.ORCID https://orcid.org/0000-0002-5119-9174
Danijela Petković RamadžaDepartment of Pediatrics University Hospital Centre Zagreb Zagreb Croatia.ORCID https://orcid.org/0000-0002-8562-153X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Asparagine synthetase deficiency (ASNSD) is a rare metabolic disease causing congenital microcephaly, severe developmental delay, and spastic quadriplegia. Although the central nervous system is severely affected, other organ systems appear unaffected by asparagine deficiency. We present an infant homozygous for the mutation c.904-1G>A in the

Indexed as

ASNS geneasparagineepilepsymicrocephalyneuronal migration

Identifiers

PMID42741518
PMCPMC13572816

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.