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Amyloid
The Journal of Protein Folding Disorders
Volume 13, 2006 - Issue 3
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Original

Myocardial hypertrophy and function are related to age at onset in familial amyloidotic polyneuropathy

, M.D., Ph.D., , , &
Pages 154-159 | Published online: 06 Jul 2009

Keep up to date with the latest research on this topic with citation updates for this article.

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Maria C. Azevedo Coutinho, Nuno Cortez-Dias, Guilhermina Cantinho, Susana Gonçalves, Nelson Cunha, Tiago Rodrigues, Laura Santos, Isabel Conceição, João Agostinho & Fausto J. Pinto. (2023) Diagnostic and prognostic contribution of DPD scintigraphy in transthyretin V30M cardiac amyloidosis. Amyloid 0:0, pages 1-10.
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Meng Jiang, Mengdie Wang, Zhengyu Tao, Yezi Chai, Qiming Liu, Qifan Lu, Qizhen Wu, Xiaoying Ying, Yanan Huang, Ying Nie, Yuqi Tang, Xin Zhang, Yu Liu & Jun Pu. (2023) Biochemical and biophysical properties of an unreported T96R mutation causing transthyretin cardiac amyloidosis. Amyloid 30:2, pages 188-198.
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Sofia Möckelind, Jan Axelsson, Björn Pilebro, Per Lindqvist, Ole B. Suhr & Torbjörn Sundström. (2020) Quantification of cardiac amyloid with [18F]Flutemetamol in patients with V30M hereditary transthyretin amyloidosis. Amyloid 27:3, pages 191-199.
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Maria C. Azevedo Coutinho, Nuno Cortez-Dias, Guilhermina Cantinho, Susana Gonçalves, Miguel Nobre Menezes, Tatiana Guimarães, Gustavo Lima da Silva, Ana Rita Francisco, João Agostinho, Laura Santos, Isabel Conceição & Fausto J. Pinto. (2020) The sensitivity of DPD scintigraphy to detect transthyretin cardiac amyloidosis in V30M mutation depends on the phenotypic expression of the disease. Amyloid 27:3, pages 174-183.
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Björn Pilebro, Ole B. Suhr, Ulf Näslund, Per Westermark, Per Lindqvist & Torbjörn Sundström. (2016) 99mTc-DPD uptake reflects amyloid fibril composition in hereditary transthyretin amyloidosis. Upsala Journal of Medical Sciences 121:1, pages 17-24.
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Elisabet Ihse, Claudio Rapezzi, Giampaolo Merlini, Merrill D. Benson, Yukio Ando, Ole B. Suhr, Shu-ichi Ikeda, Francesca Lavatelli, Laura Obici, Candida C. Quarta, Ornella Leone, Hirofumi Jono, Mitsuharu Ueda, Massimiliano Lorenzini, Juris Liepnieks, Toshinori Ohshima, Masayoshi Tasaki, Taro Yamashita & Per Westermark. (2013) Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis. Amyloid 20:3, pages 142-150.
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Ole B Suhr, Sandra Gustavsson, Victoria Heldestad, Rolf Hörnsten, Per Lindqvist, Erik Nordh & Urban Wiklund. (2012) New insights into the clinical evaluation of hereditary transthyretin amyloidosis patients: a single center’s experience. Degenerative Neurological and Neuromuscular Disease 2, pages 93-106.
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S. Okamoto, J. Wixner, B.-G. Ericzon, S. Friman, P. Lindqvist, M. Henein & O. B. Suhr. (2011) Prognostic value of pre-transplant cardiomyopathy in Swedish liver transplanted patients for familial amyloidotic polyneuropathy. Amyloid 18:sup1, pages 171-173.
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Rolf Hörnsten, Johanna Pennlert, Urban Wiklund, Per Lindqvist, Steen M. Jensen & Ole B. Suhr. (2010) Heart complications in familial transthyretin amyloidosis: impact of age and gender. Amyloid 17:2, pages 63-68.
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Ole B. Suhr, Oluf Andersen, Thomas Aronsson, Jenni Jonasson, Hannu Kalimo, Christer Lundahl, Hans-Eric Lundgren, Atle Melberg, Johan Nyberg, Malin Olsson, Arne Sandberg & Per Westermark. (2009) Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden. Amyloid 16:4, pages 208-214.
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Scott Arno & Jennifer Cowger. (2021) The genetics of cardiac amyloidosis. Heart Failure Reviews 27:5, pages 1485-1492.
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O. B. Suhr, E. Lundgren & P. Westermark. (2017) One mutation, two distinct disease variants: unravelling the impact of transthyretin amyloid fibril composition. Journal of Internal Medicine 281:4, pages 337-347.
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Sadahisa Okamoto, Rolf Hörnsten, Konen Obayashi, Priyantha Wijayatunga & Ole B. Suhr. (2011) Continuous development of arrhythmia is observed in swedish transplant patients with familial amyloidotic polyneuropathy (amyloidogenic transthyretin Val30Met variant). Liver Transplantation 17:2, pages 122-128.
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P. Kerschen & V. Planté-Bordeneuve. (2011) Neuropathies amyloïdes familiales. EMC - Neurologie 8:4, pages 1-12.
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Bárbara Macedo, Joana Magalhães, Ana Rita Batista & Maria João Saraiva. (2010) Carvedilol treatment reduces transthyretin deposition in a familial amyloidotic polyneuropathy mouse model. Pharmacological Research 62:6, pages 514-522.
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E Ihse, A Ybo, OB Suhr, P Lindqvist, C Backman & P Westermark. (2008) Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis. The Journal of Pathology 216:2, pages 253-261.
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