European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants.
- DOI
- 10.1186/s13023-019-1186-2
- Published
- 2019 Nov 21
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- cautionDOI registered: No matching Crossref record was present in this response.
- cautionDOI resolves: No matching Crossref record was present in this response.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- supportingOpen access status: Normalized open-access status: open.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty.
Cite this work
BibTeX
@article{allodium:10.1186/s13023-019-1186-2,
title = {European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants.},
author = {van de Laar IMBH and Arbustini E and Loeys B and Björck E and Murphy L and Groenink M and Kempers M and Timmermans J and Roos-Hesselink J and Benke K and Pepe G and Mulder B and Szabolcs Z and Teixidó-Turà G and Robert L and Emmanuel Y and Evangelista A and Pini A and von Kodolitsch Y and Jondeau G and De Backer J},
year = {2019},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-019-1186-2},
url = {https://doi.org/10.1186/s13023-019-1186-2}
}RIS
TY - JOUR TI - European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants. AU - van de Laar IMBH AU - Arbustini E AU - Loeys B AU - Björck E AU - Murphy L AU - Groenink M AU - Kempers M AU - Timmermans J AU - Roos-Hesselink J AU - Benke K AU - Pepe G AU - Mulder B AU - Szabolcs Z AU - Teixidó-Turà G AU - Robert L AU - Emmanuel Y AU - Evangelista A AU - Pini A AU - von Kodolitsch Y AU - Jondeau G AU - De Backer J PY - 2019 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-019-1186-2 UR - https://doi.org/10.1186/s13023-019-1186-2 ER -
APA
IMBH, V. D. L., E, A., B, L., E, B., L, M., M, G., M, K., J, T., J, R., K, B., G, P., B, M., Z, S., G, T., L, R., Y, E., A, E., A, P., Y, V. K., G, J., & J, D. B. (2019). European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-019-1186-2
Source records
- pubmed · retrieved 2026-09-25T18:32:48.552Z