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Amyloid
The Journal of Protein Folding Disorders
Volume 9, 2002 - Issue 2
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Original Article

Long-term quantitative evaluation of liver transplantation in familial amyloid polyneuropathy (Portuguese V30M)

Original Articles

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Pages 126-133 | Received 18 Jun 2001, Accepted 07 Jan 2002, Published online: 06 Jul 2009

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Read on this site (10)

Arianna Burton, Adam Castaño, Marianna Bruno, Steve Riley, Jennifer Schumacher, Marla B Sultan, Sandi See Tai, Daniel P Judge, Jignesh K Patel & Jeffery W Kelly. (2021) Drug Discovery and Development in Rare Diseases: Taking a Closer Look at the Tafamidis Story. Drug Design, Development and Therapy 15, pages 1225-1243.
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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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Shu-ichi Ikeda, Yo-ichi Takei & Yasuhiko Hashikura. (2003) Liver transplantation as treatment for neurological disorders. Expert Review of Neurotherapeutics 3:4, pages 547-555.
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José Castro, Bruno Miranda, Isabel de Castro & Isabel Conceição. (2021) Changes in nerve conduction studies predate clinical symptoms onset in early onset Val30Met hereditary ATTR amyloidosis. European Journal of Neurology 29:3, pages 826-832.
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Alejandra González‐Duarte, Isabel Conceição, Leslie Amass, Marc F. Botteman, John A. Carter & Michelle Stewart. (2020) Impact of Non-Cardiac Clinicopathologic Characteristics on Survival in Transthyretin Amyloid Polyneuropathy. Neurology and Therapy 9:1, pages 135-149.
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Massimiliano Lorenzini & Perry M Elliott. (2019) Tafamidis for the treatment of transthyretin amyloidosis. Future Cardiology 15:2, pages 53-61.
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I. Conceição, B. Miranda, J. Castro & M. de Carvalho. (2018) Hereditary amyloidosis related to transthyretin V30M: disease progression in treated and untreated patients. European Journal of Neurology 25:11, pages 1320-e115.
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Mar Guasp, Alejandro A. Köhler, Michela Campolo, Jordi Casanova-Molla & Josep Valls-Sole. (2018) Evidence of neurophysiological improvement of early manifestations of small-fiber dysfunction after liver transplantation in a patient with familial amyloid neuropathy. Clinical Neurophysiology Practice 3, pages 40-44.
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Ashutosh D Wechalekar, Julian D Gillmore & Philip N Hawkins. (2016) Systemic amyloidosis. The Lancet 387:10038, pages 2641-2654.
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Jonas Wixner, Torbjörn Sundström, Pontus Karling, Intissar Anan & Ole B Suhr. (2015) Outcome of gastric emptying and gastrointestinal symptoms after liver transplantation for hereditary transthyretin amyloidosis. BMC Gastroenterology 15:1.
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Ana Paula Barreiros, Gerd Otto, Bita Kahlen, Andreas Teufel & Peter R. Galle. (2015) Familial amyloidosis: Great progress for an orphan disease. Journal of Hepatology 62:2, pages 483-485.
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A. C. Martins, A. M. Rosa, E. Costa, C. Tavares, M. J. Quadrado & J. N. Murta. (2015) Ocular Manifestations and Therapeutic Options in Patients with Familial Amyloid Polyneuropathy: A Systematic Review. BioMed Research International 2015, pages 1-9.
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Mitsuharu Ueda & Yukio Ando. (2014) Recent advances in transthyretin amyloidosis therapy. Translational Neurodegeneration 3:1.
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Isabel Conceição, João Costa, José Castro & Mamede de Carvalho. (2014) Neurophysiological techniques to detect early small-fiber dysfunction in transthyretin amyloid polyneuropathy. Muscle & Nerve 49:2, pages 181-186.
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Merrill D. Benson. (2013) Liver transplantation and transthyretin amyloidosis. Muscle & Nerve 47:2, pages 157-162.
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Maria Teresa Tomás, Helena Santa-Clara, Paula Marta Bruno, Estela Monteiro, Margarida Carrolo, Eduardo Barroso, Luís B. Sardinha & Bo Fernhall. (2013) The Impact of Exercise Training on Liver Transplanted Familial Amyloidotic Polyneuropathy (FAP) Patients. Transplantation Journal 95:2, pages 372-377.
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David C. Seldin & Martha Skinner. 2013. Kelley's Textbook of Rheumatology. Kelley's Textbook of Rheumatology 1889 1897 .
Mamede de Carvalho. (2012) Is it better than it seems or just good enough? The tafamidis saga. Muscle & Nerve 46:6, pages 14-14.
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S. W. Dubrey & R. L. Comenzo. (2012) Amyloid diseases of the heart: current and future therapies. QJM 105:7, pages 617-631.
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Melo Beirão, Eduarda Matos, Idalina Beirão, Paulo Pinho-Costa & Paulo Torres. (2012) No ocular involvement in familial amyloidotic polyneuropathy ATTR V30M domino liver recipients. Transplant International 25:6, pages 646-651.
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Maria T. Tomás, Maria H. Santa-Clara, Estela Monteiro, Tracy Baynard, Elvis Á. Carnero, Paula M. Bruno, Eduardo Barroso, Luís B. Sardinha & Bo Fernhall. (2011) Body composition, muscle strength, functional capacity, and physical disability risk in liver transplanted familial amyloidotic polyneuropathy patients. Clinical Transplantation 25:4, pages E406-E414.
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Isabel Conceição, Teresinha Evangelista, José Castro, Pedro Pereira, Ana Silvestre, Conceição A Coutinho & Mamede de Carvalho. (2010) Acquired amyloid neuropathy in a Portuguese patient after domino liver transplantation. Muscle & Nerve 42:5, pages 836-838.
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Zachary Simmons & Charles S Specht. (2010) The Neuromuscular Manifestations of Amyloidosis. Journal of Clinical Neuromuscular Disease 11:3, pages 145-157.
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Ana-Paula Barreiros, Felix Post, Maria Hoppe-Lotichius, Reinhold P. Linke, Christian F. Vahl, Hans-Joachim Schäfers, Peter R. Galle & Gerd Otto. (2010) Liver transplantation and combined liver-heart transplantation in patients with familial amyloid polyneuropathy: A single-center experience. Liver Transplantation 16:3, pages 314-323.
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A.J. DEMETRIS, JAMES M. CRAWFORD, MARTA IDA MINERVINI, MIKE NALESNIK, ERIN OCHOA, PARMJEET RANDHAWA, EIZABURO SASATOMI & TONG WU. 2009. Surgical Pathology of the GI Tract, Liver, Biliary Tract, and Pancreas. Surgical Pathology of the GI Tract, Liver, Biliary Tract, and Pancreas 1169 1229 .
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Y. Shimojima, H. Morita, S. Kobayashi, Y. Takei & S. Ikeda. (2008) Ten-year follow-up of peripheral nerve function in patients with familial amyloid polyneuropathy after liver transplantation. Journal of Neurology 255:8, pages 1220-1225.
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Isabel M. Conceição, José F. Castro, Manuel Scotto & Mamede de Carvalho. (2008) Neurophysiological markers in familial amyloid polyneuropathy patients: Early changes. Clinical Neurophysiology 119:5, pages 1082-1087.
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Ayako Tsuchiya, Masahide Yazaki, Fuyuki Kametani, Yo-ichi Takei & Shu-ichi Ikeda. (2008) Marked regression of abdominal fat amyloid in patients with familial amyloid polyneuropathy during long-term follow-up after liver transplantation. Liver Transplantation 14:4, pages 563-570.
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M Yazaki, S Mitsuhashi, T Tokuda, F Kametani, Y-I Takei, J Koyama, A Kawamorita, H Kanno & S-I Ikeda. (2007) Progressive Wild-Type Transthyretin Deposition after Liver Transplantation Preferentially Occurs onto Myocardium in FAP Patients. American Journal of Transplantation 7:1, pages 235-242.
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Isabel Conceição & Mamede De Carvalho. (2007) Clinical variability in type I familial amyloid polyneuropathy (Val30Met): Comparison between late- and early-onset cases in Portugal. Muscle & Nerve 35:1, pages 116-118.
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Hisayasu Terazaki, Yukio Ando, Rui Fernandes, Ken-ichi Yamamura, Shuichiro Maeda & Maria J Saraiva. (2006) Immunization in familial amyloidotic polyneuropathy: counteracting deposition by immunization with a Y78F TTR mutant. Laboratory Investigation 86:1, pages 23-31.
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I. M. Conceicao, L. C. Miranda, E. Simoes, R. G. Gouveia, T. D. Evangelista & M. A. Carvalho. (2005) Bone mineral density in familial amyloid polyneuropathy and in other neuromuscular disorders. European Journal of Neurology 12:6, pages 480-482.
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Yo-ichi TAKEI, Shu-ichi IKEDA, Toshihiko IKEGAMI, Yasuhiko HASHIKURA, Shin-ichi MIYAGAWA & Yukio ANDO. (2005) Ten Years of Experience with Liver Transplantation for Familial Amyloid Polyneuropathy in Japan: Outcomes of Living Donor Liver Transplantations. Internal Medicine 44:11, pages 1151-1156.
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