European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT).

Eker OF, Boccardi E, Sure U, Patel MC, Alicante S, Alsafi A, Coote N, Droege F, Dupuis O, Fialla AD, Jones B, Kariholu U, Kjeldsen AD, Lefroy D, Lenato GM, Mager HJ, Manfredi G, Nielsen TH, Pagella F, Post MC, Rennie C, Sabbà C, Suppressa P, Toerring PM, Ugolini S, Buscarini E, Dupuis-Girod S, Shovlin CL

Open source

DOI: 10.1186/s13023-020-01386-9
Published: 2020 Jun 29
Container: Orphanet journal of rare diseases
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/s13023-020-01386-9,
  title = {European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT).},
  author = {Eker OF and Boccardi E and Sure U and Patel MC and Alicante S and Alsafi A and Coote N and Droege F and Dupuis O and Fialla AD and Jones B and Kariholu U and Kjeldsen AD and Lefroy D and Lenato GM and Mager HJ and Manfredi G and Nielsen TH and Pagella F and Post MC and Rennie C and Sabbà C and Suppressa P and Toerring PM and Ugolini S and Buscarini E and Dupuis-Girod S and Shovlin CL},
  year = {2020},
  journal = {Orphanet journal of rare diseases},
  doi = {10.1186/s13023-020-01386-9},
  url = {https://doi.org/10.1186/s13023-020-01386-9}
}

RIS

TY  - JOUR
TI  - European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT).
AU  - Eker OF
AU  - Boccardi E
AU  - Sure U
AU  - Patel MC
AU  - Alicante S
AU  - Alsafi A
AU  - Coote N
AU  - Droege F
AU  - Dupuis O
AU  - Fialla AD
AU  - Jones B
AU  - Kariholu U
AU  - Kjeldsen AD
AU  - Lefroy D
AU  - Lenato GM
AU  - Mager HJ
AU  - Manfredi G
AU  - Nielsen TH
AU  - Pagella F
AU  - Post MC
AU  - Rennie C
AU  - Sabbà C
AU  - Suppressa P
AU  - Toerring PM
AU  - Ugolini S
AU  - Buscarini E
AU  - Dupuis-Girod S
AU  - Shovlin CL
PY  - 2020
JO  - Orphanet journal of rare diseases
DO  - 10.1186/s13023-020-01386-9
UR  - https://doi.org/10.1186/s13023-020-01386-9
ER  -

APA

OF, E., E, B., U, S., MC, P., S, A., A, A., N, C., F, D., O, D., AD, F., B, J., U, K., AD, K., D, L., GM, L., HJ, M., G, M., TH, N., F, P., MC, P., C, R., C, S., P, S., PM, T., S, U., E, B., S, D., & CL, S. (2020). European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT).. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-020-01386-9

Source records

pubmed · retrieved 2026-09-25T21:03:43.712Z