Výsledky vyhledávání - "AMYLOIDOSIS"

Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases Autor Garcia-Pavia, Pablo, Rapezzi, Claudio, Adler, Yehuda, Arad, Michael, Basso, Cristina, Brucato, Antonio, Burazor, Ivana, Caforio, Alida L P, Damy, Thibaud, Eriksson, Urs, Fontana, Marianna, Gillmore, Julian D, Gonzalez-Lopez, Esther, Grogan, Martha, Heymans, Stephane, Imazio, Massimo, Kindermann, Ingrid, Kristen, Arnt V, Maurer, Mathew S, Merlini, Giampaolo, Pantazis, Antonis, Pankuweit, Sabine, Rigopoulos, Angelos G, Linhart, Ales

“…Cardiac amyloidosis is a serious and progressive infiltrative disease that is caused by the deposition of amyloid fibrils at the cardiac level. It can be due…”
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S3830 A Gastrointestinal Bleeding Mystery: Uncovering Localized Gastric Amyloidosis Autor Mekheal, Nader, Bathobakae, Lefika, Farokhian, Alisa, Alkomos, Mina, Elagami, Mohamed, Volfson, Ariy, Baddoura, Walid, Cavanagh, Yana

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Primary localized cutaneous amyloidosis of lower leg with 12years follow‐up Autor Deo, Neha, Gibson, Lawrence, Johnson, Emma, Alavi, Afsaneh

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Patisiran Treatment in Patients with Transthyretin Cardiac Amyloidosis Autor Maurer, Mathew S., Kale, Parag, Fontana, Marianna, Berk, John L., Grogan, Martha, Gustafsson, Finn, Hung, Rebecca R., Gottlieb, Robert L., Damy, Thibaud, González-Duarte, Alejandra, Sarswat, Nitasha, Sekijima, Yoshiki, Tahara, Nobuhiro, Taylor, Mark S., Kubanek, Milos, Donal, Erwan, Palecek, Tomas, Tsujita, Kenichi, Tang, W.H. Wilson, Yu, Wen-Chung, Obici, Laura, Simões, Marcus, Fernandes, Fábio, Poulsen, Steen Hvitfeldt, Diemberger, Igor, Perfetto, Federico, Solomon, Scott D., Di Carli, Marcelo, Badri, Prajakta, White, Matthew T., Chen, Jihong, Yureneva, Elena, Sweetser, Marianne T., Jay, Patrick Y., Garg, Pushkal P., Vest, John, Gillmore, Julian D.

“…This phase 3 trial of patisiran, a small interfering RNA that targets hepatic production of the transthyretin protein, showed efficacy in treating…”
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Reply to the Letter to the Editor: "The Need for a New Description of Red Flags in Cardiac Amyloidosis in Turkish Population"/ Editore Mektup Yaniti: Turk Toplumunda Kardiyak Amiloidozda Kirmizi Bayraklarin Yeni Bir Tanimina Olan Ihtiyac Autor Murat, Selda, Yalvac, Halit Emre, Cavusoglu, Yuksel

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Investigating Cardiac Amyloidosis: A Primer for Clinicians Autor Bukhari, Syed, Bashir, Zubair, Shah, Nishant, Patel, Yash, Hulten, Edward

“…Cardiac amyloidosis (CA) is an infiltrative disease that results from the deposition of amyloid fibrils in the myocardium, resulting in restrictive…”
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Daratumumab-Based Treatment for Immunoglobulin Light-Chain Amyloidosis Autor Kastritis, Efstathios, Palladini, Giovanni, Minnema, Monique C, Wechalekar, Ashutosh D, Jaccard, Arnaud, Lee, Hans C, Sanchorawala, Vaishali, Gibbs, Simon, Mollee, Peter, Venner, Christopher P, Lu, Jin, Schönland, Stefan, Gatt, Moshe E, Suzuki, Kenshi, Kim, Kihyun, Cibeira, M. Teresa, Beksac, Meral, Libby, Edward, Valent, Jason, Hungria, Vania, Wong, Sandy W, Rosenzweig, Michael, Bumma, Naresh, Huart, Antoine, Dimopoulos, Meletios A, Bhutani, Divaya, Waxman, Adam J, Goodman, Stacey A, Zonder, Jeffrey A, Lam, Selay, Song, Kevin, Hansen, Timon, Manier, Salomon, Roeloffzen, Wilfried, Jamroziak, Krzysztof, Kwok, Fiona, Shimazaki, Chihiro, Kim, Jin-Seok, Crusoe, Edvan, Ahmadi, Tahamtan, Tran, NamPhuong, Qin, Xiang, Vasey, Sandra Y, Tromp, Brenda, Schecter, Jordan M, Weiss, Brendan M, Zhuang, Sen H, Vermeulen, Jessica, Merlini, Giampaolo, Comenzo, Raymond L

“…In a randomized trial of bortezomib, cyclophosphamide, and dexamethasone as compared with the same therapy plus daratumumab, patients with light-chain…”
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Skeletal muscle involvement in systemic amyloidosis is often overlooked Autor Xu, Jingwen, Zhou, Xiaoyu, Wang, Yingxin, Liu, Wenzhu, Shan, Yi, Zhang, Dong, Lv, Huixia, Zhao, Dandan, Dai, Tingjun, Zhao, Yuying, Li, Wei, Liu, Fuchen, Yan, Chuanzhu

“…Aim Systemic amyloidosis is a condition in which misfolded amyloid fibrils are deposited within tissues. Amyloid myopathy is a rare manifestation of systemic…”
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Amyloid and Light Chain Deposition Disorders Autor Baqir, Misbah, Moua, Teng, Ryu, Jay H

“…Amyloidosis and Light Chain Deposition Disease (LCDD) are disorders characterized by the deposition of abnormal proteins in tissues, leading to organ damage…”
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Aortic Stenosis and Cardiac Amyloidosis: JACC Review Topic of the Week Autor Ternacle, Julien, Krapf, Laura, Mohty, Dania, Magne, Julien, Nguyen, Annabelle, Galat, Arnault, Gallet, Romain, Teiger, Emmanuel, Côté, Nancy, Clavel, Marie-Annick, Tournoux, François, Pibarot, Philippe, Damy, Thibaud

“…The prevalence of calcific aortic stenosis (AS) and of cardiac amyloidosis (CA) increases with age, and their association is not uncommon in the elderly. The…”
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AL type renal amyloidosis with cardiac involvement: A case report and literature review Autor Sun, Yang, Zhao, Yan-Hong, Wang, Qiong-Fen, Yang, Shan-Lan, Yang, Yu-Juan, Yang, Xiao-Yu, Liu, Ming-Wei

“…Systemic amyloidosis refers to a spectrum of diseases characterized by extracellular deposition of amyloids, with commonrenal involvement; however,…”
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Natural course of Finnish gelsolin amyloidosis Autor Nikoskinen, Tuuli, Schmidt, Eeva-Kaisa, Strbian, Daniel, Kiuru-Enari, Sari, Atula, Sari

“…Background. Finnish type of hereditary gelsolin amyloidosis (FGA) is one of the most common diseases of Finnish disease heritage. Existing FGA knowledge is…”
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The spectrum of pulmonary amyloidosis Autor Riehani, Anas, Soubani, Ayman O

“…Amyloidosis is a disease caused by misfolded proteins that deposit in the extracellular matrix as fibrils, resulting in the dysfunction of the involved organ…”
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AL Amyloidosis Autor Desport, Estelle, Bridoux, Frank, Sirac, Christophe, Delbes, Sébastien, Bender, Sébastien, Fernandez, Béatrice, Quellard, Nathalie, Lacombe, Corinne, Goujon, Jean-Michel, Lavergne, David, Abraham, Julie, Touchard, Guy, Fermand, Jean-Paul, Jaccard, Arnaud

“…Definition of the disease AL amyloidosis results from extra-cellular deposition of fibril-forming monoclonal immunoglobulin (Ig) light chains (LC) (most…”
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Myocardial work indices in the short‐term prognosis of light‐chain cardiac amyloidosis: Incremental value beyond traditional staging models and echocardiographic parameters Autor Meng, Fangmin, Li, Jing, Zhao, Rui, Wu, Yuanfeng, Liu, Yu, Yang, Yiming, Yang, Yang, Zhou, Nianwei, Dong, Lili, Kong, Dehong, Chen, Haiyan, Shu, Xianhong, Liu, Peng, Pan, Cuizhen

“…Summary Light‐chain cardiac amyloidosis (AL‐CA) causes structural and functional cardiac impairment. Myocardial work (MW), integrating left ventricular strain…”
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Thrombotic and bleeding complications in patients with AL amyloidosis Autor Fotiou, Despina, Theodorakakou, Foteini, Spiliopoulou, Sotiria, Gavriatopoulou, Maria, Migkou, Magdalini, Kanellias, Nikolaos, Eleutherakis‐Papaiakovou, Evangelos, Malandrakis, Panagiotis, Dialoupi, Ioanna, Roussou, Maria, Ntanasis‐Stathopoulos, Ioannis, Terpos, Evangelos, Dimopoulos, Meletios A., Kastritis, Efstathios

“…Haemostatic abnormalities and deregulated coagulation are common complications in AL amyloidosis. The relevant risks of thromboembolic and haemorrhagic events…”
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Protein Misfolding, Amyloid Formation, and Human Disease: A Summary of Progress Over the Last Decade Autor Chiti, Fabrizio, Dobson, Christopher M

“…Peptides and proteins have been found to possess an inherent tendency to convert from their native functional states into intractable amyloid aggregates. This…”
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Diagnostic performance of imaging investigations in detecting and differentiating cardiac amyloidosis: a systematic review and meta‐analysis Autor Brownrigg, Jack, Lorenzini, Massimiliano, Lumley, Matthew, Elliott, Perry

“…Aims The study aims to systematically assess the diagnostic performance of cardiac magnetic resonance (CMR) and nuclear scintigraphy (index tests) for the…”
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Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association Autor Kittleson, Michelle M, Maurer, Mathew S, Ambardekar, Amrut V, Bullock-Palmer, Renee P, Chang, Patricia P, Eisen, Howard J, Nair, Ajith P, Nativi-Nicolau, Jose, Ruberg, Frederick L

“…Transthyretin amyloid cardiomyopathy (ATTR-CM) results in a restrictive cardiomyopathy caused by extracellular deposition of transthyretin, normally involved…”
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State-of-the-art review on AL amyloidosis in Western Countries: Epidemiology, health economics, risk assessment and therapeutic management of a rare disease Autor Sabinot, Alice, Ghetti, Gianni, Pradelli, Lorenzo, Bellucci, Stefania, Lausi, Antonella, Palladini, Giovanni

“…Amyloidosis is the term to define a broad array of rare protein misfolding syndromes. Among them, light chain (AL) amyloidosis is the most common, affecting…”
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