Case study: Gly53Ala transthyretin amyloidosis with small fibre sensory and autonomic neuropathy and cardiac involvement

Autor: Andersen, A, Rasmussen, T, Molgaard, H, Obal, I, Moller, A, Terkelsen, A

Publikováno v: Andersen, A, Rasmussen, T, Molgaard, H, Obal, I, Moller, A & Terkelsen, A 2021, ' Case study: Gly53Ala transthyretin amyloidosis with small fibre sensory and autonomic neuropathy and cardiac involvement ', European Journal of Neurology, vol. 28, no. S1, pp. 540 . < https://onlinelibrary.wiley.com/toc/14681331/2021/28/S1 >

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::718ef30987ce442896af873b1e011d5b
https://vbn.aau.dk/da/publications/4f75c94f-9403-4583-8152-737b1fb7c0c3

Sex-Related Risk of Cardiac Involvement in Hereditary Transthyretin Amyloidosis: Insights From THAOS

Autor: Caponetti, A. G., Rapezzi, C., Gagliardi, C., Milandri, A., Dispenzieri, A., Kristen, A. V., Wixner, J., Maurer, M. S., Garcia-Pavia, P., Tournev, I., Plante-Bordeneuve, V., Chapman, D., Amass, L., van Cleemput, J., Waddington-Cruz, M., Schmidt, H., Dillmann, K. -U., Molgaard, H., Moreno, J. G., Costello, J. G., Beamud, F. M., Davila, L. G., Adams, D., Inamo, J., Lairez, O., Vita, G., Merlini, G., Cirami, C. L., Luigetti, M., Emdin, M., Sekijima, Y., Jeon, E. -S., Oh, J., Gonzalez Duarte Briseno, M. A., Nienhuis, H., Coelho, T., Conceicao, I., Azevedo, O., Badelita, S., Press, R., Parman, Y., Shah, S., Quan, D., Marburger, T., Polydefkis, M., Witteles, R., Gottlieb, S., Sarswat, N., Drachman, B., Steidley, D., Hummel, S., Slosky, D., Jacoby, D., Nativi-Nicolau, J., Tauras, J., Zivkovic, S., Tallaj, J., Lenihan, D.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3709::da1446f1e60664906d1418d8099eaa5e
https://hdl.handle.net/11392/2472809

PRO28 LIFETIME HOSPITAL COSTS OF DANISH PATIENTS SUFFERING FROM LEU111MET TRANSTHYRETIN AMYLOID CARDIOMYOPATHY

Autor: Pilgaard, T., Pedersen, M., Strand, A., Poulsen, S., Mølgaard, H.

Publikováno v: In Value in Health May 2020 23 Supplement 1:S333-S333

The Majority of Plakophilin-2 Mutations in Arrhythmogenic Cardiomyopathy are Associated with Haploinsufficiency in the Myocardium and Epidermis

Autor: Rasmussen, TB, Nissen, PH, Palmfeldt, J, Gehmlich, K, Dalager, S, Jensen, UB, Kim, WY, Heickendorff, L, Molgaard, H, Jensen, HK, Baandrup, UT, Bross, P, Mogensen, J

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2ddf75a611847681ce4a5a5f899fdf70
https://ora.ox.ac.uk/objects/uuid:f78c9a78-0ac0-4b16-b35e-3c9351d6958d

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