Epigallocatechin-3-gallate tolerability and impact on survival in a cohort of patients with transthyretin-related cardiac amyloidosis. A single-center retrospective study
暂无分享,去创建一个
C. Di Mario | S. Bartolini | F. Perfetto | F. Cappelli | G. Taborchi | S. Morini | S. Farsetti | Paola Angelotti | R. Martone | Sofia Morini
[1] A. Petrie,et al. A new staging system for cardiac transthyretin amyloidosis , 2018, European heart journal.
[2] W. Litchy,et al. Trial design and rationale for APOLLO, a Phase 3, placebo-controlled study of patisiran in patients with hereditary ATTR amyloidosis with polyneuropathy , 2017, BMC Neurology.
[3] Sanjiv J. Shah,et al. Design and Rationale of the Phase 3 ATTR-ACT Clinical Trial (Tafamidis in Transthyretin Cardiomyopathy Clinical Trial). , 2017, Circulation. Heart failure.
[4] A. Dispenzieri,et al. Natural History of Wild-Type Transthyretin Cardiac Amyloidosis and Risk Stratification Using a Novel Staging System. , 2016, Journal of the American College of Cardiology.
[5] P. Hawkins,et al. Systemic amyloidosis , 2016, The Lancet.
[6] James C Moon,et al. Nonbiopsy Diagnosis of Cardiac Transthyretin Amyloidosis , 2016, Circulation.
[7] S. Frusconi,et al. The Val142Ile transthyretin cardiac amyloidosis: not only an Afro-American pathogenic variant? A single-centre Italian experience , 2016, Journal of cardiovascular medicine.
[8] H. Katus,et al. Green tea extract as a treatment for patients with wild-type transthyretin amyloidosis: an observational study , 2015, Drug design, development and therapy.
[9] B. Bettencourt,et al. Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose study , 2015, Orphanet Journal of Rare Diseases.
[10] Victor Mor-Avi,et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. , 2015, European heart journal cardiovascular Imaging.
[11] H. Katus,et al. Extracellular remodeling in patients with wild-type amyloidosis consuming epigallocatechin-3-gallate: preliminary results of T1 mapping by cardiac magnetic resonance imaging in a small single center study , 2015, Clinical Research in Cardiology.
[12] Victor Mor-Avi,et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. , 2015, Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography.
[13] E. Nordh,et al. Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial. , 2013, JAMA.
[14] F. Salvi,et al. Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective. , 2013, European heart journal.
[15] M. Saraiva,et al. Natural polyphenols as modulators of TTR amyloidogenesis: in vitro and in vivo evidences towards therapy , 2012, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.
[16] M. Gobbi,et al. Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: a phase II study , 2012, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.
[17] E. Wanker,et al. Green tea halts progression of cardiac transthyretin amyloidosis: an observational report , 2012, Clinical Research in Cardiology.
[18] M. Saraiva,et al. Epigallocatechin-3-Gallate as a Potential Therapeutic Drug for TTR-Related Amyloidosis: “In Vivo” Evidence from FAP Mice Models , 2012, PloS one.
[19] L. Padeletti,et al. Cardiac amyloidosis: the heart of the matter , 2013, Internal and Emergency Medicine.
[20] F. Perfetto,et al. Asymptomatic homozygous gene carrier in a family with Ile68Leu ATTR amyloidosis: a new endemic region in northern Tuscany? , 2011, Journal of cardiovascular medicine.
[21] H. Katus,et al. Effects of the main green tea polyphenol epigallocatechin-3-gallate on cardiac involvement in patients with AL amyloidosis , 2010, Clinical Research in Cardiology.
[22] S. Sang,et al. Hepatotoxicity of high oral dose (-)-epigallocatechin-3-gallate in mice. , 2010, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
[23] M. Saraiva,et al. Binding of epigallocatechin‐3‐gallate to transthyretin modulates its amyloidogenicity , 2009, FEBS letters.
[24] D. Ehrnhoefer,et al. EGCG redirects amyloidogenic polypeptides into unstructured, off-pathway oligomers , 2008, Nature Structural &Molecular Biology.
[25] W. Hunstein. Epigallocathechin-3-gallate in AL amyloidosis: a new therapeutic option? , 2007, Blood.
[26] R. Falk,et al. Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): A consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis , 2005, American journal of hematology.