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

por Andersen, Poul Erik, Kjeldsen, Anette D
Publicado 2012

ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasia

por Tørring, Pernille M., Kjeldsen, Anette D., Ousager, Lilian Bomme, Brusgaard, Klaus
Publicado en Mol Genet Genomic Med (2017)

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

por Olsen, Lilian B., Kjeldsen, Anette D., Poulsen, Mikael K., Kjeldsen, Jens, Fialla, Annette D.
Publicado en Orphanet J Rare Dis (2020)

Long Non-Coding RNA Expression Profiles in Hereditary Haemorrhagic Telangiectasia

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

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

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

Complement Defects in Patients with Chronic Rhinosinusitis

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

Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia

por 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.
Publicado en 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)

por 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.
Publicado en Orphanet J Rare Dis (2020)