Hereditary haemorrhagic telangiectasia: a population‐based study of prevalence and mortality in Danish patients von Kjeldsen, A. D., Vase, P., Green, A.

Volltext

The Sinonasal Outcome Test 22 score in persons without chronic rhinosinusitis von Lange, B., Thilsing, T., Baelum, J., Kjeldsen, A.D.

Volltext

JP-HHT phenotype in Danish patients with SMAD4 mutations von Jelsig, A. M., Tørring, P. M., Kjeldsen, A. D., Qvist, N., Bojesen, A., Jensen, U. B., Andersen, M. K., Gerdes, A. M., Brusgaard, K., Ousager, L. B.

Volltext

National mutation study among Danish patients with hereditary haemorrhagic telangiectasia von Tørring, P.M., Brusgaard, K., Ousager, L.B., Andersen, P.E., Kjeldsen, A.D.

Volltext

Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia von KJELDSEN, A. D., MØLLER, T. R., BRUSGAARD, K., VASE, P., ANDERSEN, P. E.

Volltext

The validity of nasal endoscopy in patients with chronic rhinosinusitis—An inter‐rater agreement study von Larsen, K.L., Lange, B., Darling, P., Jørgensen, G., Kjeldsen, A.D.

Volltext

Prevalence of pulmonary arteriovenous malformations (PAVMs) and occurrence of neurological symptoms in patients with hereditary haemorrhagic telangiectasia (HHT) von Kjeldsen, A. D., Oxhøj, H., Andersen, P. E., Green, A., Vase, P.

Volltext

Efficacy of ESS in chronic rhinosinusitis with and without nasal polyposis: a Danish cohort study von Lind, Henrik, Joergensen, G., Lange, B., Svendstrup, F., Kjeldsen, A. D.

Volltext

The European Rare Disease Network for HHT Frameworks for management of hereditary haemorrhagic telangiectasia in general and speciality care von Shovlin, C.L., Buscarini, E., Sabbà, C., Mager, H.J., Kjeldsen, A.D., Pagella, F., Sure, U., Ugolini, S., Torring, P.M., Suppressa, P., Rennie, C., Post, M.C., Patel, M.C., Nielsen, T.H., Manfredi, G., Lenato, G.M., Lefroy, D., Kariholu, U., Jones, B., Fialla, A.D., Eker, O.F., Dupuis, O., Droege, F., Coote, N., Boccardi, E., Alsafi, A., Alicante, S., Dupuis-Girod, S.

Volltext

Prevalence of hereditary hemorrhagic telangiectasia in patients operated for cerebral abscess: a retrospective cohort analysis von Larsen, L., Marker, C. R., Kjeldsen, A. D., Poulsen, F. R.

Volltext

Pulmonary arteriovenous malformations: a radiological and clinical investigation of 136 patients with long-term follow-up von Andersen, P.E., Tørring, P.M., Duvnjak, S., Gerke, O., Nissen, H., Kjeldsen, A.D.

Volltext

Pulmonary arteriovenous malformations : Screening procedures and pulmonary angiography in patients with Hereditary hemorrhagic telangiectasia von KJELDSEN, A. D, OXHØJ, H, ANDERSEN, P. E, ELLE, B, JACOBSEN, J. P, VASE, P

Volltext

Mutations in endoglin and in activin receptor-like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia von Brusgaard, K, Kjeldsen, AD, Poulsen, L, Moss, H, Vase, P, Rasmussen, K, Kruse, TA, Hørder, M

Volltext

Middle ear disease in Danish toddlers attending nursery day-care – Applicability of OM-6, disease specific quality of life and predictors for middle ear symptoms von Indius, J.H., Alqaderi, S.K., Kjeldsen, A.D., Heidemann, C.H.

Volltext

Occlusion of Pulmonary Arteriovenous Malformations by Use of Vascular Plug von Andersen, P. E., Kjeldsen, A. D.

Volltext

Concerning the original article of C. Weik and L. Greiner, 'The liver in hereditary hemorrhagic telangiectasia (Weber-Renduosler disease)' von Kjeldsen, A D, Kjeldsen, J

Volltext

Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome) von Shovlin, Claire L., Guttmacher, Alan E., Buscarini, Elisabetta, Faughnan, Marie E., Hyland, Robert H., Westermann, Cornelius J.J., Kjeldsen, Anette D., Plauchu, Henri

Volltext

Embolotherapy for Pulmonary Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Syndrome) von Andersen, Poul Erik, Kjeldsen, A. Drøhse, Oxhøj, H., Vase, P., White, R. I.

Volltext

Tympanoplasty with Ionomeric Cement von D. Kjeldsen, Aksel M. Grøntved, Anette

Volltext

Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia von 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

Volltext