Recommendations update for the diagnosis and treatment of transthyretin variant amyloidosis (ATTRv)

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Published inMedicina clínica (English ed.) Vol. 163; no. 6; pp. e69 - e77
Main Authors González-Moreno, Juan, Galán Dávila, Lucía, Gonzalez-Lopez, Esther, Conceiçao, Isabel, Barriales-Villa, Roberto, Falcão de Campos, Catarina, Cardoso, Márcio Neves, Casasnovas, Carlos, Fernández-Martín, Julián, Morales, Raúl Juntas, López, Inés Losada, Martínez-Vicente, Laura, Muñoz-Beamud, Francisco, Quintana, Luis F., Sevilla, Teresa
Format Journal Article
LanguageEnglish
Published Elsevier España, S.L.U 27.09.2024
Online AccessGet full text
ISSN2387-0206
2387-0206
DOI10.1016/j.medcle.2024.04.011

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Author Cardoso, Márcio Neves
Sevilla, Teresa
Gonzalez-Lopez, Esther
González-Moreno, Juan
Conceiçao, Isabel
Fernández-Martín, Julián
Barriales-Villa, Roberto
Casasnovas, Carlos
Galán Dávila, Lucía
Morales, Raúl Juntas
López, Inés Losada
Quintana, Luis F.
Falcão de Campos, Catarina
Muñoz-Beamud, Francisco
Martínez-Vicente, Laura
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  givenname: Márcio Neves
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  fullname: Cardoso, Márcio Neves
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  givenname: Carlos
  surname: Casasnovas
  fullname: Casasnovas, Carlos
  organization: Neuromuscular Unit, Neurology Department, Hospital Universitari de Bellvitge, IDIBELL and CIBERER, l'Hospitalet de Llobregat, Barcelona, Spain
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  surname: Fernández-Martín
  fullname: Fernández-Martín, Julián
  organization: Internal Medicine Department, Hospital Alvaro Cunqueiro, Vigo, Pontevedra, Spain
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  surname: Morales
  fullname: Morales, Raúl Juntas
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  givenname: Luis F.
  surname: Quintana
  fullname: Quintana, Luis F.
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  givenname: Teresa
  surname: Sevilla
  fullname: Sevilla, Teresa
  organization: Neurology Service, Hospital Universitari i Politècnic La Fe/IISLAFE, University of Valencia, CIBERER (ERN EURO-NMD), Valencia, Spain
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Cites_doi 10.1136/jnnp-2014-308724
10.1016/j.jaccao.2021.06.006
10.1111/jns.12451
10.1002/ejhf.2198
10.1007/s40265-019-01129-6
10.1097/WCO.0000000000000852
10.1080/13506129.2022.2147636
10.1080/13506129.2018.1436048
10.1016/j.clinph.2020.01.022
10.1056/NEJMoa1805689
10.1055/s-0039-1688977
10.2337/dc10-1303
10.1016/j.recesp.2019.12.017
10.1080/13506129.2017.1292902
10.3390/brainsci10120989
10.1080/13506129.2019.1685487
10.1016/j.healun.2017.11.015
10.1080/13506129.2018.1556156
10.1016/j.medcli.2020.06.064
10.1093/eurheartj/ehab072
10.1161/CIRCULATIONAHA.118.035831
10.3109/13506129.2015.1015678
10.1080/13506129.2022.2091985
10.1080/13506129.2016.1272453
10.1111/ajt.17009
10.1016/S1474-4422(11)70246-0
10.1186/1750-1172-8-31
10.1016/j.jcmg.2019.07.015
10.1080/13506129.2018.1564903
10.1016/j.jacc.2017.05.053
10.1378/chest.104.2.618
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References Adams, Slama (bib0120) 2020; 33
Tozza, Severi, Spina, Iovino, Aruta, Ruggiero (bib0030) 2021; 26
Maurer, Schwartz, Gundapaneni, Elliott, Merlini, Waddington-Cruz (bib0130) 2018; 379
Solomon, Adams, Kristen, Grogan, González-Duarte, Maurer (bib0110) 2019; 139
Pollak, Falk (bib0140) 1993; 104
Garcia-Pavia, Rapezzi, Adler, Arad, Basso, Brucato (bib0060) 2021; 42
Dasgupta, Rissing, Smith, Jung, Benson (bib0105) 2020; 27
Ohashi, Kodaira, Morita, Sekijima (bib0090) 2019; 26
Zhou (bib0040) 2019; 39
Kristen, Kreusser, Blum, Schönland, Frankenstein, Dösch (bib0145) 2018; 37
Conceição, Damy, Romero, Galán, Attarian, Luigetti (bib0025) 2019; 26
Ando, Coelho, Berk, Cruz, Ericzon, Ikeda (bib0020) 2013; 20
Garcia-Pavia, Bengel, Brito, Damy, Duca, Dorbala (bib0155) 2021; 23
Lamb, Deeks (bib0100) 2019; 79
Buxbaum, Dispenzieri, Eisenberg, Fändrich, Merlini, Saraiva (bib0015) 2022; 29
Tesfaye, Boulton, Dyck, Freeman, Horowitz, Kempler (bib0055) 2010; 33
López-Sainz, Hernández-Hernández, González-López, Domínguez, Restrepo-Córdoba, Cobo-Marcos (bib0065) 2021; 74
Griffin, Rosenthal, Grodin, Maurer, Grogan, Cheng (bib0150) 2021; 3
Nolano, Tozza, Caporaso, Provitera (bib0045) 2020; 10
Planté-Bordeneuve, Said (bib0035) 2011; 0
Aus dem Siepen, Hein, Bauer, Katus, Kristen (bib0135) 2017; 24
Fortanier, Delmont, Verschueren, Attarian (bib0050) 2020; 131
Phull, Sanchorawala, Connors, Doros, Ruberg, Berk (bib0095) 2018; 25
Garcia-Pavia, Domínguez, Gonzalez-Lopez (bib0075) 2021; 156
Cruz, Schmidt, Botteman, Carter, Chopra, Stewart (bib0010) 2017; 24
Sekijima (bib0005) 2015; 86
Martinez-Naharro, Treibel, Abdel-Gadir, Bulluck, Zumbo, Knight (bib0080) 2017; 70
Dorbala, Cuddy, Falk (bib0070) 2020; 13
Beirão, Malheiro, Lemos, Beirão, Costa, Torres (bib0085) 2015; 22
Adams, Tournev, Taylor, Coelho, Planté-Bordeneuve, Berk (bib0115) 2023; 30
Schmidt, Wixner, Planté-Bordeneuve, Muñoz-Beamud, Lladó, Gillmore (bib0125) 2022; 22
Aus dem Siepen (10.1016/j.medcle.2024.04.011_bib0135) 2017; 24
Planté-Bordeneuve (10.1016/j.medcle.2024.04.011_bib0035) 2011; 0
Schmidt (10.1016/j.medcle.2024.04.011_bib0125) 2022; 22
Lamb (10.1016/j.medcle.2024.04.011_bib0100) 2019; 79
Nolano (10.1016/j.medcle.2024.04.011_bib0045) 2020; 10
Garcia-Pavia (10.1016/j.medcle.2024.04.011_bib0060) 2021; 42
López-Sainz (10.1016/j.medcle.2024.04.011_bib0065) 2021; 74
Solomon (10.1016/j.medcle.2024.04.011_bib0110) 2019; 139
Beirão (10.1016/j.medcle.2024.04.011_bib0085) 2015; 22
Ohashi (10.1016/j.medcle.2024.04.011_bib0090) 2019; 26
Pollak (10.1016/j.medcle.2024.04.011_bib0140) 1993; 104
Dorbala (10.1016/j.medcle.2024.04.011_bib0070) 2020; 13
Garcia-Pavia (10.1016/j.medcle.2024.04.011_bib0075) 2021; 156
Buxbaum (10.1016/j.medcle.2024.04.011_bib0015) 2022; 29
Martinez-Naharro (10.1016/j.medcle.2024.04.011_bib0080) 2017; 70
Kristen (10.1016/j.medcle.2024.04.011_bib0145) 2018; 37
Tesfaye (10.1016/j.medcle.2024.04.011_bib0055) 2010; 33
Ando (10.1016/j.medcle.2024.04.011_bib0020) 2013; 20
Adams (10.1016/j.medcle.2024.04.011_bib0115) 2023; 30
Adams (10.1016/j.medcle.2024.04.011_bib0120) 2020; 33
Fortanier (10.1016/j.medcle.2024.04.011_bib0050) 2020; 131
Conceição (10.1016/j.medcle.2024.04.011_bib0025) 2019; 26
Griffin (10.1016/j.medcle.2024.04.011_bib0150) 2021; 3
Zhou (10.1016/j.medcle.2024.04.011_bib0040) 2019; 39
Cruz (10.1016/j.medcle.2024.04.011_bib0010) 2017; 24
Garcia-Pavia (10.1016/j.medcle.2024.04.011_bib0155) 2021; 23
Dasgupta (10.1016/j.medcle.2024.04.011_bib0105) 2020; 27
Phull (10.1016/j.medcle.2024.04.011_bib0095) 2018; 25
Maurer (10.1016/j.medcle.2024.04.011_bib0130) 2018; 379
Tozza (10.1016/j.medcle.2024.04.011_bib0030) 2021; 26
Sekijima (10.1016/j.medcle.2024.04.011_bib0005) 2015; 86
References_xml – volume: 86
  start-page: 1036
  year: 2015
  end-page: 1043
  ident: bib0005
  article-title: Transthyretin (ATTR) amyloidosis: clinical spectrum, molecular pathogenesis and disease-modifying treatments
  publication-title: J Neurol Neurosurg Psychiatry
– volume: 29
  start-page: 213
  year: 2022
  end-page: 219
  ident: bib0015
  article-title: Amyloid nomenclature 2022: update, novel proteins, and recommendations by the International Society of Amyloidosis (ISA) Nomenclature Committee
  publication-title: Amyloid
– volume: 26
  start-page: 15
  year: 2019
  end-page: 23
  ident: bib0090
  article-title: Electrophysiological demyelinating features in hereditary ATTR amyloidosis
  publication-title: Amyloid
– volume: 10
  start-page: 989
  year: 2020
  ident: bib0045
  article-title: Contribution of skin biopsy in peripheral neuropathies
  publication-title: Brain Sci
– volume: 379
  start-page: 1007
  year: 2018
  end-page: 1016
  ident: bib0130
  article-title: Tafamidis treatment for patients with transthyretin amyloid cardiomyopathy
  publication-title: N Engl J Med
– volume: 30
  start-page: 1
  year: 2023
  end-page: 9
  ident: bib0115
  article-title: Efficacy and safety of vutrisiran for patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy: a randomized clinical trial
  publication-title: Amyloid
– volume: 22
  start-page: 1646
  year: 2022
  end-page: 1657
  ident: bib0125
  article-title: Patisiran treatment in patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy after liver transplantation
  publication-title: Am J Transplant
– volume: 23
  start-page: 895
  year: 2021
  end-page: 905
  ident: bib0155
  article-title: Expert consensus on the monitoring of transthyretin amyloid cardiomyopathy
  publication-title: Eur J Heart Fail
– volume: 70
  start-page: 466
  year: 2017
  end-page: 477
  ident: bib0080
  article-title: Magnetic resonance in transthyretin cardiac amyloidosis
  publication-title: J Am Coll Cardiol
– volume: 0
  start-page: 1086
  year: 2011
  end-page: 1097
  ident: bib0035
  article-title: Familial amyloid polyneuropathy
  publication-title: Lancet Neurol
– volume: 33
  start-page: 2285
  year: 2010
  end-page: 2293
  ident: bib0055
  article-title: Diabetic neuropathies: update on definitions, diagnostic criteria, estimation of severity, and treatments
  publication-title: Diabetes Care
– volume: 79
  start-page: 863
  year: 2019
  end-page: 874
  ident: bib0100
  article-title: Tafamidis: a review in transthyretin amyloidosis with polyneuropathy
  publication-title: Drugs
– volume: 26
  start-page: 155
  year: 2021
  end-page: 159
  ident: bib0030
  article-title: The neuropathy in hereditary transthyretin amyloidosis: a narrative review
  publication-title: J Peripher Nerv Syst
– volume: 156
  start-page: 126
  year: 2021
  end-page: 134
  ident: bib0075
  article-title: Transthyretin amyloid cardiomyopathy
  publication-title: Med Clin (Barc)
– volume: 37
  start-page: 611
  year: 2018
  end-page: 618
  ident: bib0145
  article-title: Improved outcomes after heart transplantation for cardiac amyloidosis in the modern era
  publication-title: J Heart Lung Transplant
– volume: 104
  start-page: 618
  year: 1993
  end-page: 620
  ident: bib0140
  article-title: Left ventricular systolic dysfunction precipitated by verapamil in cardiac amyloidosis
  publication-title: Chest
– volume: 22
  start-page: 117
  year: 2015
  end-page: 122
  ident: bib0085
  article-title: Ophthalmological manifestations in hereditary transthyretin (ATTR V30M) carriers: a review of 513 cases
  publication-title: Amyloid
– volume: 26
  start-page: 3
  year: 2019
  end-page: 9
  ident: bib0025
  article-title: Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations
  publication-title: Amyloid
– volume: 13
  start-page: 1368
  year: 2020
  end-page: 1383
  ident: bib0070
  article-title: How to image cardiac amyloidosis: a practical approach
  publication-title: JACC Cardiovasc Imaging
– volume: 25
  start-page: 62
  year: 2018
  end-page: 67
  ident: bib0095
  article-title: Monoclonal gammopathy of undetermined significance in systemic transthyretin amyloidosis (ATTR)
  publication-title: Amyloid
– volume: 24
  start-page: 132
  year: 2017
  end-page: 133
  ident: bib0135
  article-title: Standard heart failure medication in cardiac transthyretin amyloidosis: useful or harmful?
  publication-title: Amyloid
– volume: 24
  start-page: 109
  year: 2017
  end-page: 110
  ident: bib0010
  article-title: Epidemiological and clinical characteristics of persons with transthyretin hereditary amyloid polyneuropathy: a global synthesis of 532 cases
  publication-title: Amyloid
– volume: 39
  start-page: 570
  year: 2019
  end-page: 577
  ident: bib0040
  article-title: Small fiber neuropathy
  publication-title: Semin Neurol
– volume: 131
  start-page: 1129
  year: 2020
  end-page: 1133
  ident: bib0050
  article-title: Quantitative sudomotor test helps differentiate transthyretin familial amyloid polyneuropathy from chronic inflammatory demyelinating polyneuropathy
  publication-title: Clin Neurophysiol
– volume: 74
  start-page: 149
  year: 2021
  end-page: 158
  ident: bib0065
  article-title: Perfil clínico y evolución de la amiloidosis cardiaca en un centro español de referencia
  publication-title: Rev Española Cardiol
– volume: 3
  start-page: 488
  year: 2021
  end-page: 505
  ident: bib0150
  article-title: ATTR amyloidosis: current and emerging management strategies: JACC: cardiooncology state-of-the-art review
  publication-title: JACC CardioOncol
– volume: 33
  start-page: 553
  year: 2020
  end-page: 561
  ident: bib0120
  article-title: Hereditary transthyretin amyloidosis: current treatment
  publication-title: Curr Opin Neurol
– volume: 42
  start-page: 1554
  year: 2021
  end-page: 1568
  ident: bib0060
  article-title: Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases
  publication-title: Eur Heart J
– volume: 139
  start-page: 431
  year: 2019
  end-page: 443
  ident: bib0110
  article-title: Effects of patisiran, an RNA interference therapeutic, on cardiac parameters in patients with hereditary transthyretin-mediated amyloidosis
  publication-title: Circulation
– volume: 20
  start-page: 31
  year: 2013
  ident: bib0020
  article-title: Guideline of transthyretin-related hereditary amyloidosis for clinicians
  publication-title: Orphanet J Rare Dis
– volume: 27
  start-page: 52
  year: 2020
  end-page: 58
  ident: bib0105
  article-title: Inotersen therapy of transthyretin amyloid cardiomyopathy
  publication-title: Amyloid
– volume: 86
  start-page: 1036
  year: 2015
  ident: 10.1016/j.medcle.2024.04.011_bib0005
  article-title: Transthyretin (ATTR) amyloidosis: clinical spectrum, molecular pathogenesis and disease-modifying treatments
  publication-title: J Neurol Neurosurg Psychiatry
  doi: 10.1136/jnnp-2014-308724
– volume: 3
  start-page: 488
  year: 2021
  ident: 10.1016/j.medcle.2024.04.011_bib0150
  article-title: ATTR amyloidosis: current and emerging management strategies: JACC: cardiooncology state-of-the-art review
  publication-title: JACC CardioOncol
  doi: 10.1016/j.jaccao.2021.06.006
– volume: 26
  start-page: 155
  year: 2021
  ident: 10.1016/j.medcle.2024.04.011_bib0030
  article-title: The neuropathy in hereditary transthyretin amyloidosis: a narrative review
  publication-title: J Peripher Nerv Syst
  doi: 10.1111/jns.12451
– volume: 23
  start-page: 895
  year: 2021
  ident: 10.1016/j.medcle.2024.04.011_bib0155
  article-title: Expert consensus on the monitoring of transthyretin amyloid cardiomyopathy
  publication-title: Eur J Heart Fail
  doi: 10.1002/ejhf.2198
– volume: 79
  start-page: 863
  year: 2019
  ident: 10.1016/j.medcle.2024.04.011_bib0100
  article-title: Tafamidis: a review in transthyretin amyloidosis with polyneuropathy
  publication-title: Drugs
  doi: 10.1007/s40265-019-01129-6
– volume: 33
  start-page: 553
  year: 2020
  ident: 10.1016/j.medcle.2024.04.011_bib0120
  article-title: Hereditary transthyretin amyloidosis: current treatment
  publication-title: Curr Opin Neurol
  doi: 10.1097/WCO.0000000000000852
– volume: 29
  start-page: 213
  year: 2022
  ident: 10.1016/j.medcle.2024.04.011_bib0015
  article-title: Amyloid nomenclature 2022: update, novel proteins, and recommendations by the International Society of Amyloidosis (ISA) Nomenclature Committee
  publication-title: Amyloid
  doi: 10.1080/13506129.2022.2147636
– volume: 25
  start-page: 62
  year: 2018
  ident: 10.1016/j.medcle.2024.04.011_bib0095
  article-title: Monoclonal gammopathy of undetermined significance in systemic transthyretin amyloidosis (ATTR)
  publication-title: Amyloid
  doi: 10.1080/13506129.2018.1436048
– volume: 131
  start-page: 1129
  year: 2020
  ident: 10.1016/j.medcle.2024.04.011_bib0050
  article-title: Quantitative sudomotor test helps differentiate transthyretin familial amyloid polyneuropathy from chronic inflammatory demyelinating polyneuropathy
  publication-title: Clin Neurophysiol
  doi: 10.1016/j.clinph.2020.01.022
– volume: 379
  start-page: 1007
  year: 2018
  ident: 10.1016/j.medcle.2024.04.011_bib0130
  article-title: Tafamidis treatment for patients with transthyretin amyloid cardiomyopathy
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa1805689
– volume: 39
  start-page: 570
  year: 2019
  ident: 10.1016/j.medcle.2024.04.011_bib0040
  article-title: Small fiber neuropathy
  publication-title: Semin Neurol
  doi: 10.1055/s-0039-1688977
– volume: 33
  start-page: 2285
  year: 2010
  ident: 10.1016/j.medcle.2024.04.011_bib0055
  article-title: Diabetic neuropathies: update on definitions, diagnostic criteria, estimation of severity, and treatments
  publication-title: Diabetes Care
  doi: 10.2337/dc10-1303
– volume: 74
  start-page: 149
  year: 2021
  ident: 10.1016/j.medcle.2024.04.011_bib0065
  article-title: Perfil clínico y evolución de la amiloidosis cardiaca en un centro español de referencia
  publication-title: Rev Española Cardiol
  doi: 10.1016/j.recesp.2019.12.017
– volume: 24
  start-page: 109
  year: 2017
  ident: 10.1016/j.medcle.2024.04.011_bib0010
  article-title: Epidemiological and clinical characteristics of persons with transthyretin hereditary amyloid polyneuropathy: a global synthesis of 532 cases
  publication-title: Amyloid
  doi: 10.1080/13506129.2017.1292902
– volume: 10
  start-page: 989
  year: 2020
  ident: 10.1016/j.medcle.2024.04.011_bib0045
  article-title: Contribution of skin biopsy in peripheral neuropathies
  publication-title: Brain Sci
  doi: 10.3390/brainsci10120989
– volume: 27
  start-page: 52
  year: 2020
  ident: 10.1016/j.medcle.2024.04.011_bib0105
  article-title: Inotersen therapy of transthyretin amyloid cardiomyopathy
  publication-title: Amyloid
  doi: 10.1080/13506129.2019.1685487
– volume: 37
  start-page: 611
  year: 2018
  ident: 10.1016/j.medcle.2024.04.011_bib0145
  article-title: Improved outcomes after heart transplantation for cardiac amyloidosis in the modern era
  publication-title: J Heart Lung Transplant
  doi: 10.1016/j.healun.2017.11.015
– volume: 26
  start-page: 3
  year: 2019
  ident: 10.1016/j.medcle.2024.04.011_bib0025
  article-title: Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations
  publication-title: Amyloid
  doi: 10.1080/13506129.2018.1556156
– volume: 156
  start-page: 126
  year: 2021
  ident: 10.1016/j.medcle.2024.04.011_bib0075
  article-title: Transthyretin amyloid cardiomyopathy
  publication-title: Med Clin (Barc)
  doi: 10.1016/j.medcli.2020.06.064
– volume: 42
  start-page: 1554
  year: 2021
  ident: 10.1016/j.medcle.2024.04.011_bib0060
  article-title: Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases
  publication-title: Eur Heart J
  doi: 10.1093/eurheartj/ehab072
– volume: 139
  start-page: 431
  year: 2019
  ident: 10.1016/j.medcle.2024.04.011_bib0110
  article-title: Effects of patisiran, an RNA interference therapeutic, on cardiac parameters in patients with hereditary transthyretin-mediated amyloidosis
  publication-title: Circulation
  doi: 10.1161/CIRCULATIONAHA.118.035831
– volume: 22
  start-page: 117
  year: 2015
  ident: 10.1016/j.medcle.2024.04.011_bib0085
  article-title: Ophthalmological manifestations in hereditary transthyretin (ATTR V30M) carriers: a review of 513 cases
  publication-title: Amyloid
  doi: 10.3109/13506129.2015.1015678
– volume: 30
  start-page: 1
  year: 2023
  ident: 10.1016/j.medcle.2024.04.011_bib0115
  article-title: Efficacy and safety of vutrisiran for patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy: a randomized clinical trial
  publication-title: Amyloid
  doi: 10.1080/13506129.2022.2091985
– volume: 24
  start-page: 132
  year: 2017
  ident: 10.1016/j.medcle.2024.04.011_bib0135
  article-title: Standard heart failure medication in cardiac transthyretin amyloidosis: useful or harmful?
  publication-title: Amyloid
  doi: 10.1080/13506129.2016.1272453
– volume: 22
  start-page: 1646
  year: 2022
  ident: 10.1016/j.medcle.2024.04.011_bib0125
  article-title: Patisiran treatment in patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy after liver transplantation
  publication-title: Am J Transplant
  doi: 10.1111/ajt.17009
– volume: 0
  start-page: 1086
  year: 2011
  ident: 10.1016/j.medcle.2024.04.011_bib0035
  article-title: Familial amyloid polyneuropathy
  publication-title: Lancet Neurol
  doi: 10.1016/S1474-4422(11)70246-0
– volume: 20
  start-page: 31
  year: 2013
  ident: 10.1016/j.medcle.2024.04.011_bib0020
  article-title: Guideline of transthyretin-related hereditary amyloidosis for clinicians
  publication-title: Orphanet J Rare Dis
  doi: 10.1186/1750-1172-8-31
– volume: 13
  start-page: 1368
  year: 2020
  ident: 10.1016/j.medcle.2024.04.011_bib0070
  article-title: How to image cardiac amyloidosis: a practical approach
  publication-title: JACC Cardiovasc Imaging
  doi: 10.1016/j.jcmg.2019.07.015
– volume: 26
  start-page: 15
  year: 2019
  ident: 10.1016/j.medcle.2024.04.011_bib0090
  article-title: Electrophysiological demyelinating features in hereditary ATTR amyloidosis
  publication-title: Amyloid
  doi: 10.1080/13506129.2018.1564903
– volume: 70
  start-page: 466
  year: 2017
  ident: 10.1016/j.medcle.2024.04.011_bib0080
  article-title: Magnetic resonance in transthyretin cardiac amyloidosis
  publication-title: J Am Coll Cardiol
  doi: 10.1016/j.jacc.2017.05.053
– volume: 104
  start-page: 618
  year: 1993
  ident: 10.1016/j.medcle.2024.04.011_bib0140
  article-title: Left ventricular systolic dysfunction precipitated by verapamil in cardiac amyloidosis
  publication-title: Chest
  doi: 10.1378/chest.104.2.618
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