Evidence map›Paper›PMID 35300531›Full record

ArticleStroke2022

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Family Members With a Pathogenic

Remco J Hack, Gido Gravesteijn, Minne N Cerfontaine, Ingrid M Hegeman, Aat A Mulder, Saskia A J Lesnik Oberstein, Julie W Rutten

Open access · hybridAbstract read
In one paragraph

Article in Stroke, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL.Annals of clinical and translational neurology · 2026
    Article
  2. Article
  3. Review
  4. Observational
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Association ofNeurology · 2024
    Article
  11. Article
  12. Advances in Management of the Stroke Etiology One-Percenters.Current neurology and neuroscience reports · 2023
    Review
  13. Phenotypic variability in 446 CADASIL patients: Impact of NOTCH3 gene mutation location in addition to the effects of age, sex and vascular risk factors.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Article
  14. Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Remco J HackDepartment of Clinical Genetics (R.J.H., G.G., M.N.C., S.A.J.L.O., J.W.R.), Leiden University Medical Center, the Netherlands.ORCID 0000-0001-9302-5802
Gido GravesteijnDepartment of Clinical Genetics (R.J.H., G.G., M.N.C., S.A.J.L.O., J.W.R.), Leiden University Medical Center, the Netherlands.ORCID 0000-0002-2610-8728
Minne N CerfontaineDepartment of Clinical Genetics (R.J.H., G.G., M.N.C., S.A.J.L.O., J.W.R.), Leiden University Medical Center, the Netherlands.ORCID 0000-0001-9357-270X
Ingrid M HegemanDepartment of Pathology (I.M.H.), Leiden University Medical Center, the Netherlands.
Aat A MulderDepartment of Cell and Chemical Biology (A.A.M.), Leiden University Medical Center, the Netherlands.ORCID 0000-0002-4779-099X
Saskia A J Lesnik Oberstein *Department of Clinical Genetics (R.J.H., G.G., M.N.C., S.A.J.L.O., J.W.R.), Leiden University Medical Center, the Netherlands.ORCID 0000-0002-1268-8995
Julie W Rutten *Department of Clinical Genetics (R.J.H., G.G., M.N.C., S.A.J.L.O., J.W.R.), Leiden University Medical Center, the Netherlands.ORCID 0000-0003-3250-7263
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo determine whether extremely mild small vessel disease (SVD) phenotypes can occur in

methodsIndividuals from CADASIL pedigrees fulfilling criteria for extremely mild

resultsSeven cases were identified that fulfilled the mSVD

conclusionsOur findings demonstrate that extremely mild SVD phenotypes can occur in individuals from CADASIL pedigrees harboring

Indexed as

CADASILLeukoencephalopathiesBiopsyBrainCross-Sectional StudiesErbB ReceptorsHumansMagnetic Resonance ImagingMutationReceptor, Notch3Receptors, NotchErbB ReceptorsNOTCH3 protein, humanReceptor, Notch3Receptors, Notchbiopsybraincapillariesvascular dementiawhite matter

Identifiers

PMID35300531
PMCPMC9126263
OpenAlexW4220733094

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.