European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

Ingrid De Graaf - van de Laar; E Arbustini; B Loeys; E Bjorck; L Murphy; M Groenink; M Kempers; J Timmermans; Jolien Roos - Hesselink; K Benke; G Pepe; B Mulder; Z Szabolcs; G Teixido-Tura; L Robert; Y Emmanuel; A Evangelista; A Pini; Y von Kodolitsch; G Jondeau; J Backer

doi:10.1186/s13023-019-1186-2

European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

Ingrid De Graaf - van de Laar
, E Arbustini
, B Loeys
, E Bjorck
, L Murphy
, M Groenink
, M Kempers
, J Timmermans
, Jolien Roos - Hesselink
, K Benke
, G Pepe
, B Mulder
, Z Szabolcs
, G Teixido-Tura
, L Robert
, Y Emmanuel
, A Evangelista
, A Pini
, Y von Kodolitsch
, G Jondeau

J Backer

Research output: Contribution to journal › Article › Academic › peer-review

38 Citations (Scopus)

38 Downloads (Pure)

Original language	Undefined/Unknown
Article number	264
Journal	Orphanet Journal of Rare Diseases
Volume	14
Issue number	1
DOIs	https://doi.org/10.1186/s13023-019-1186-2
Publication status	Published - 2019

Research programs

EMC COEUR-09

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10.1186/s13023-019-1186-2

Repub_121991_O-A.pdfFinal published version, 514 KB

Cite this

De Graaf - van de Laar, I., Arbustini, E., Loeys, B., Bjorck, E., Murphy, L., Groenink, M., Kempers, M., Timmermans, J., Roos - Hesselink, J., Benke, K., Pepe, G., Mulder, B., Szabolcs, Z., Teixido-Tura, G., Robert, L., Emmanuel, Y., Evangelista, A., Pini, A., von Kodolitsch, Y., ... Backer, J. (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, 14(1), Article 264. https://doi.org/10.1186/s13023-019-1186-2

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De Graaf - van de Laar, I, Arbustini, E, Loeys, B, Bjorck, E, Murphy, L, Groenink, M, Kempers, M, Timmermans, J, Roos - Hesselink, J, Benke, K, Pepe, G, Mulder, B, Szabolcs, Z, Teixido-Tura, G, Robert, L, Emmanuel, Y, Evangelista, A, Pini, A, von Kodolitsch, Y, Jondeau, G & Backer, J 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, vol. 14, no. 1, 264. https://doi.org/10.1186/s13023-019-1186-2

European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants. / De Graaf - van de Laar, Ingrid; Arbustini, E; Loeys, B et al.
In: Orphanet Journal of Rare Diseases, Vol. 14, No. 1, 264, 2019.

Research output: Contribution to journal › Article › Academic › peer-review

TY - JOUR

T1 - European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

AU - De Graaf - van de Laar, Ingrid

AU - Arbustini, E

AU - Loeys, B

AU - Bjorck, E

AU - Murphy, L

AU - Groenink, M

AU - Kempers, M

AU - Timmermans, J

AU - Roos - Hesselink, Jolien

AU - Benke, K

AU - Pepe, G

AU - Mulder, B

AU - Szabolcs, Z

AU - Teixido-Tura, G

AU - Robert, L

AU - Emmanuel, Y

AU - Evangelista, A

AU - Pini, A

AU - von Kodolitsch, Y

AU - Jondeau, G

AU - Backer, J

PY - 2019

Y1 - 2019

U2 - 10.1186/s13023-019-1186-2

DO - 10.1186/s13023-019-1186-2

M3 - Article

SN - 1750-1172

VL - 14

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

IS - 1

M1 - 264

ER -