Zobrazeno 1 - 10
of 112
pro vyhledávání: '"amyloidosi"'
Autor:
Lyon, A. R., Lopez-Fernandez, T., Couch, L. S., Asteggiano, R., Aznar, M. C., Bergler-Klein, J., Boriani, G., Cardinale, D., Cordoba, R., Cosyns, B., Cutter, D. J., de Azambuja, E., de Boer, R. A., Dent, S. F., Farmakis, D., Gevaert, S. A., Gorog, D. A., Herrmann, J., Lenihan, D., Moslehi, J., Moura, B., Salinger, S. S., Stephens, R., Suter, T. M., Szmit, S., Tamargo, J., Thavendiranathan, P., Tocchetti, C. G., van der Meer, P., van der Pal, H. J. H., Lancellotti, P., Thuny, F., Abdelhamid, M., Aboyans, V., Aleman, B., Alexandre, J., Barac, A., Borger, M. A., Casado-Arroyo, R., Cautela, J., Celutkiene, J., Cikes, M., Cohen-Solal, A., Dhiman, K., Ederhy, S., Edvardsen, T., Fauchier, L., Fradley, M., Grapsa, J., Halvorsen, S., Heuser, M., Humbert, M., Jaarsma, T., Kahan, T., Konradi, A., Koskinas, K. C., Kotecha, D., Ky, B., Landmesser, U., Lewis, B. S., Linhart, A., Lip, G. Y. H., Lochen, M. -L., Malaczynska-Rajpold, K., Metra, M., Mindham, R., Moonen, M., Neilan, T. G., Nielsen, J. C., Petronio, A. -S., Prescott, E., Rakisheva, A., Salem, J. -E., Savarese, G., Sitges, M., Ten Berg, J., Touyz, R. M., Tycinska, A., Wilhelm, M., Zamorano, J. L.
Publikováno v:
European Heart Journal-Cardiovascular Imaging, 23(10). Oxford University Press
European Heart Journal, 43(41), 4229-4361. Oxford University Press
Lyon, A R, López-Fernández, T, Couch, L S, Asteggiano, R, Aznar, M C, Bergler-Klein, J, Boriani, G, Cardinale, D, Cordoba, R, Cosyns, B, Cutter, D J, de Azambuja, E, de Boer, R A, Dent, S F, Farmakis, D, Gevaert, S A, Gorog, D A, Herrmann, J, Lenihan, D, Moslehi, J, Moura, B, Salinger, S S, Stephens, R, Suter, T M, Szmit, S, Tamargo, J, Thavendiranathan, P, Tocchetti, C G, van der Meer, P, van der Pal, H J H & ESC Scientific Document Group 2022, ' 2022 ESC Guidelines on cardio-oncology developed in collaboration with the European Hematology Association (EHA), the European Society for Therapeutic Radiology and Oncology (ESTRO) and the International Cardio-Oncology Society (IC-OS) : Developed by the task force on cardio-oncology of the European Society of Cardiology (ESC) ', European Heart Journal Cardiovascular Imaging, vol. 23, no. 10, pp. e333-e465 . https://doi.org/10.1093/ehjci/jeac106
European Heart Journal, 43(41), 4229-4361. Oxford University Press
Lyon, A R, López-Fernández, T, Couch, L S, Asteggiano, R, Aznar, M C, Bergler-Klein, J, Boriani, G, Cardinale, D, Cordoba, R, Cosyns, B, Cutter, D J, de Azambuja, E, de Boer, R A, Dent, S F, Farmakis, D, Gevaert, S A, Gorog, D A, Herrmann, J, Lenihan, D, Moslehi, J, Moura, B, Salinger, S S, Stephens, R, Suter, T M, Szmit, S, Tamargo, J, Thavendiranathan, P, Tocchetti, C G, van der Meer, P, van der Pal, H J H & ESC Scientific Document Group 2022, ' 2022 ESC Guidelines on cardio-oncology developed in collaboration with the European Hematology Association (EHA), the European Society for Therapeutic Radiology and Oncology (ESTRO) and the International Cardio-Oncology Society (IC-OS) : Developed by the task force on cardio-oncology of the European Society of Cardiology (ESC) ', European Heart Journal Cardiovascular Imaging, vol. 23, no. 10, pp. e333-e465 . https://doi.org/10.1093/ehjci/jeac106
Autor:
Lacetera R., Roggero L., Vercelloni P., Uzzo M., Carbone M., Invernizzi P., L'Imperio V., Pieruzzi F., Sinico R. A.
Publikováno v:
Case Reports in Nephrology and Dialysis. 12:178-184
AA amyloidosis may complicate several chronic inflammatory conditions. From a clinical point of view, causality between inflammatory pathology and AA amyloidosis can be assumed because of the data described in the literature; some of the best known i
Publikováno v:
Cardiovascular Research. 118:3517-3535
Transthyretin cardiac amyloidosis (ATTR-CA) is an increasingly recognized cause of heart failure (HF) and mortality worldwide. Advances in non-invasive diagnosis, coupled with the development of effective treatments, have shifted ATTR-CA from a rare
Autor:
Stefano Tozza, Daniele Severi, Emanuele Spina, Andrea Di Paolantonio, Aniello Iovino, Valeria Guglielmino, Francesco Aruta, Maria Nolano, Mario Sabatelli, Lucio Santoro, Marco Luigetti, Fiore Manganelli
Publikováno v:
Journal of Neurology. 269:4281-4287
Background Hereditary transthyretin amyloidosis (ATTRv) is a rare, debilitating and fatal disease, mostly characterized by progressive axonal peripheral neuropathy. Diagnosis is still challenging and diagnostic delay in non-endemic area is about 3–
Autor:
Vincenzo Nuzzi, Aldostefano Porcari, Marta Gigli, Francesco Zaja, Franca Dore, Rossana Bussani, Gianfranco Sinagra, Marco Merlo
Publikováno v:
European Heart Journal - Case Reports. 7
BackgroundCardiac involvement in amyloid light-chain (AL) amyloidosis usually represents a brick in the wall of a multi-system disease. The presence of cardiac deposition of free light chains (FLCs) is the main determinant of survival. Isolated cardi
Autor:
Francesca Re, Sofia Giorgetti, Barbara Biondi, Stefano Scapin, Francesco Mantegazza, Valeria Cassina, Silvia Maria Sesana, Laura Rizzi, Ivano Eberini, Luca Palazzolo, Marten Beeg, Marco Gobbi, Marco Sardina, Massimo Masserini
The effect of liposomes bi-functionalized with phosphatidic acid and with a synthetic peptide derived from human apolipoprotein E has been evaluated on the aggregation features of different amyloidogenic proteins: human Amyloid β1–40 (Aβ1–40),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a29e89b1d8aa048b0fb8a4e6a3b4248
Autor:
Sinagra G., Emdin M., Merlo M., Vergaro G., Aimo A., Biagini E., Imazio M., Porcari A., Limongelli G., Cipriani A., Canepa M., Musumeci B., Cameli M., Crotti L., Di Bella G., Di Lenarda A., Cappelli F., Chimenti C., Obici L., Iacoviello M., Perlini S., Pieroni M., Metra M., Oliva F., Perrone Filardi P., Colivicchi F., Indolfi C.
The perspective on amyloidosis has changed deeply over the last 10 years following major advances in diagnosis and treatment options, especially in cardiac amyloidosis. This intrinsically heterogeneous disease exposes to the risk of fragmentation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1299::53ddf1e9ce21307fc6face451b0ca653
https://hdl.handle.net/10281/404301
https://hdl.handle.net/10281/404301
Autor:
Sinagra, Gianfranco, Emdin, Michele, Merlo, Marco, Vergaro, Giuseppe, Aimo, Alberto, Biagini, Elena, Imazio, Massimo, Porcari, Aldostefano, Limongelli, Giuseppe, Cipriani, Alberto, Canepa, Marco, Musumeci, Beatrice, Cameli, Matteo, Crotti, Lia, Di Bella, Gianluca, Di Lenarda, Andrea, Cappelli, Francesco, Chimenti, Cristina, Obici, Laura, Iacoviello, Massimo, Perlini, Stefano, Pieroni, Maurizio, Metra, Marco, Oliva, Fabrizio, Perrone Filardi, Pasquale, Colivicchi, Furio, Indolfi, Ciro
The perspective on amyloidosis has changed deeply over the last 10 years following major advances in diagnosis and treatment options, especially in cardiac amyloidosis. This intrinsically heterogeneous disease exposes to the risk of fragmentation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b7babd77572aee26ffc0a44a0d804711
https://hdl.handle.net/11368/3039558
https://hdl.handle.net/11368/3039558
ObjectivesAmyloid light chain (AL)-κ and AL-λ share common histopathologic changes; however, the potential difference in clinical manifestations, histologic findings, and clinical significance between the 2 subtypes remain unclear.MethodsIn a retro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::625cd24c337d41199dd4b829dbae03d4
https://hdl.handle.net/10281/406016
https://hdl.handle.net/10281/406016
Autor:
Aimo, Alberto, Tomasoni, Daniela, Porcari, Aldostefano, Vergaro, Giuseppe, Castiglione, Vincenzo, Passino, Claudio, Adamo, Marianna, Bellicini, Maria Giulia, Lombardi, Carlo Mario, Nardi, Matilde, Palamara, Gloria, Varrà, Guerino Giuseppe, Saro, Riccardo, Allegro, Valentina, Merlo, Marco, Sinagra, Gianfranco, Metra, Marco, Emdin, Michele, Rapezzi, Claudio
Aims: Cardiac amyloidosis (CA) is due to a deposition of amyloid fibrils in the heart causing an increase in wall thickness. A left ventricular (LV) wall thickness ≥12 mm plus at least one red flag should raise the suspicion of CA. As normal values
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b33bee46c103d44a868702cd52fae21
https://hdl.handle.net/11368/3041581
https://hdl.handle.net/11368/3041581