Embolization of pulmonary AVMs of feeding arteries less than 3 mm: reports of two cases and an 8-year follow-up without embolization

gan Andersen, Poul Erik, Kjeldsen, Anette D
Cyhoeddwyd 2012

ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasia

gan Tørring, Pernille M., Kjeldsen, Anette D., Ousager, Lilian Bomme, Brusgaard, Klaus
Cyhoeddwyd yn Mol Genet Genomic Med (2017)

High output cardiac failure in 3 patients with hereditary hemorrhagic telangiectasia and hepatic vascular malformations, evaluation of treatment

gan Olsen, Lilian B., Kjeldsen, Anette D., Poulsen, Mikael K., Kjeldsen, Jens, Fialla, Annette D.
Cyhoeddwyd yn Orphanet J Rare Dis (2020)

Long Non-Coding RNA Expression Profiles in Hereditary Haemorrhagic Telangiectasia

gan Tørring, Pernille M., Larsen, Martin Jakob, Kjeldsen, Anette D., Ousager, Lilian Bomme, Tan, Qihua, Brusgaard, Klaus
Cyhoeddwyd 2014

Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia

gan Aagaard, Katrine S., Brusgaard, Klaus, Miceikaite, Ieva, Larsen, Martin J., Kjeldsen, Anette D., Lester, Emilie B., Ousager, Lilian B., Tørring, Pernille M.
Cyhoeddwyd yn Mol Genet Genomic Med (2020)

Complement Defects in Patients with Chronic Rhinosinusitis

gan Gaunsbaek, Maria Q., Lange, Bibi, Kjeldsen, Anette D., Svane-Knudsen, Viggo, Skjoedt, Karsten, Henriksen, Maiken L., Nielsen, Christian, Palarasah, Yaseelan, Hansen, Soren
Cyhoeddwyd 2012

Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia

gan Buscarini, Elisabetta, Botella, Luisa Maria, Geisthoff, Urban, Kjeldsen, Anette D., Mager, Hans Jurgen, Pagella, Fabio, Suppressa, Patrizia, Zarrabeitia, Roberto, Dupuis-Girod, Sophie, Shovlin, Claire L.
Cyhoeddwyd yn Orphanet J Rare Dis (2019)

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

gan Eker, Omer F., Boccardi, Edoardo, Sure, Ulrich, Patel, Maneesh C., Alicante, Saverio, Alsafi, Ali, Coote, Nicola, Droege, Freya, Dupuis, Olivier, Fialla, Annette Dam, Jones, Bryony, Kariholu, Ujwal, Kjeldsen, Anette D., Lefroy, David, Lenato, Gennaro M., Mager, Hans Jurgen, Manfredi, Guido, Nielsen, Troels H., Pagella, Fabio, Post, Marco C., Rennie, Catherine, Sabbà, Carlo, Suppressa, Patrizia, Toerring, Pernille M., Ugolini, Sara, Buscarini, Elisabetta, Dupuis-Girod, Sophie, Shovlin, Claire L.
Cyhoeddwyd yn Orphanet J Rare Dis (2020)