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Amyloid
The Journal of Protein Folding Disorders
Volume 22, 2015 - Issue 3
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Original Article

Can echocardiography and ECG discriminate hereditary transthyretin V30M amyloidosis from hypertrophic cardiomyopathy?

Sandra GustavssonDivision of Clinical Physiology, Heart Centre and Department of Public Health and Clinical Medicine, Correspondence[email protected]
,
Gabriel GranåsenDepartment of Radiation Sciences,
,
Christer GrönlundDepartment of Radiation Sciences, ;Center for Biomedical Engineering and Physics (CMTF),
,
Urban WiklundDepartment of Radiation Sciences,
,
Stellan MörnerDepartment of Public Health and Clinical Medicine, and
,
Michael HeneinDepartment of Public Health and Clinical Medicine, and
,
Ole B SuhrDepartment of Public Health and Clinical Medicine, and
&
Per LindqvistDivision of Clinical Physiology, Heart Centre and Department of Surgical and Perioperative Sciences, Umeå University, Umeå, Sweden
 show all
Pages 163-170 | Received 16 Oct 2014, Accepted 01 Apr 2015, Published online: 24 Jun 2015

Citations (11)

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Read on this site (2)

Bennett Di Giovanni, Dakota Gustafson & Diego Hernan Delgado. (2019) Amyloid transthyretin cardiac amyloidosis: diagnosis and management. Expert Review of Cardiovascular Therapy 17:9, pages 673-681.
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Eve Cariou, Youssef Bennani Smires, Gérard Victor, Guillaume Robin, David Ribes, Pierre Pascal, Antoine Petermann, Pauline Fournier, Stanislas Faguer, Jérôme Roncalli, Hervé Rousseau, Dominique Chauveau, Didier Carrié, Isabelle Berry, Michel Galinier & Olivier Lairez. (2017) Diagnostic score for the detection of cardiac amyloidosis in patients with left ventricular hypertrophy and impact on prognosis. Amyloid 24:2, pages 101-109.
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Articles from other publishers (9)

Issa Pour-Ghaz, Anandbir Bath, Sharif Kayali, Deya Alkhatib, Neeraja Yedlapati, Isaac Rhea, Rami N. Khouzam, John L. Jefferies & Mannu Nayyar. (2022) A Review of Cardiac Amyloidosis: Presentation, Diagnosis, and Treatment. Current Problems in Cardiology 47:12, pages 101366.
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M. Y. Henein, B. Pilebro & Per Lindqvist. (2022) Disease progression in cardiac morphology and function in heart failure: ATTR cardiac amyloidosis versus hypertensive left ventricular hypertrophy. Heart and Vessels 37:9, pages 1562-1569.
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S. S. Nikitin, S. N. Bardakov, N. A. Suponeva, I. V. Zhirov, T. A. Adyan, D. A. Grishina & R. V. Deev. (2021) Phenotypic heterogeneity and diagnostic features of transthyretin amyloidosis with polyneuropathy. Neuromuscular Diseases 11:3, pages 12-36.
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Takayuki Inomata, Nobuhiro Tahara, Kazufumi Nakamura, Jin Endo, Mitsuharu Ueda, Tomonori Ishii, Yoshinobu Kitano & Jun Koyama. (2021) Diagnosis of wild‐type transthyretin amyloid cardiomyopathy in Japan: red‐flag symptom clusters and diagnostic algorithm. ESC Heart Failure 8:4, pages 2647-2659.
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Viktor Löfbacka, Ole B. Suhr, Bjorn Pilebro, Jonas Wixner, Torbjorn Sundström, Krister Lindmark, Intissar Anan & Per Lindqvist. (2021) Combining ECG and echocardiography to identify transthyretin cardiac amyloidosis in heart failure. Clinical Physiology and Functional Imaging.
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Morie Gertz, David Adams, Yukio Ando, João Melo Beirão, Sabahat Bokhari, Teresa Coelho, Raymond L. Comenzo, Thibaud Damy, Sharmila Dorbala, Brian M. Drachman, Marianna Fontana, Julian D. Gillmore, Martha Grogan, Philip N. Hawkins, Isabelle Lousada, Arnt V. Kristen, Frederick L. Ruberg, Ole B. Suhr, Mathew S. Maurer, Jose Nativi-Nicolau, Candida Cristina Quarta, Claudio Rapezzi, Ronald Witteles & Giampaolo Merlini. (2020) Avoiding misdiagnosis: expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner. BMC Family Practice 21:1.
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Anatoli Kiotsekoglou, Samir K. Saha, Navin C. Nanda & Per Lindqvist. (2020) Echocardiographic diagnosis of cardiac amyloidosis: Does the masquerader require only a "cherry on top"?. Echocardiography 37:11, pages 1713-1715.
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Nicolas Junqua, Damien Legallois, Sophie Segard, Olivier Lairez, Patricia Réant, Cyril Goizet, Hélène Maillard, Philippe Charron, Paul Milliez & Fabien Labombarda. (2020) The value of electrocardiography and echocardiography in distinguishing Fabry disease from sarcomeric hypertrophic cardiomyopathy. Archives of Cardiovascular Diseases 113:8-9, pages 542-550.
Crossref
Yoshimichi Miyazaki. (2017) Treatment of transthyretin familial amyloid polyneuropathy with tafamidis: a case report. Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics 54:1, pages 75-80.
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