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

بواسطة Andersen, Poul Erik, Kjeldsen, Anette D
منشور في 2012

ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasia

بواسطة Tørring, Pernille M., Kjeldsen, Anette D., Ousager, Lilian Bomme, Brusgaard, Klaus
الحاوية / القاعدة Mol Genet Genomic Med (2017)

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

بواسطة Olsen, Lilian B., Kjeldsen, Anette D., Poulsen, Mikael K., Kjeldsen, Jens, Fialla, Annette D.
الحاوية / القاعدة Orphanet J Rare Dis (2020)

Long Non-Coding RNA Expression Profiles in Hereditary Haemorrhagic Telangiectasia

بواسطة Tørring, Pernille M., Larsen, Martin Jakob, Kjeldsen, Anette D., Ousager, Lilian Bomme, Tan, Qihua, Brusgaard, Klaus
منشور في 2014

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

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

Complement Defects in Patients with Chronic Rhinosinusitis

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

Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia

بواسطة 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.
الحاوية / القاعدة 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)

بواسطة 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.
الحاوية / القاعدة Orphanet J Rare Dis (2020)