Hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: disease profile and differential diagnosis with hypertrophic cardiomyopathy and senile systemic amyloidosis

被引：0
|
作者：
Quarta, C. [1 ]
Obici, L. [2 ]
Longhi, S. [1 ]
Perlini, S. [2 ]
Milandri, A. [1 ]
Del Corso, F. [1 ]
Perfetto, F. [3 ]
Cappelli, F. [3 ]
Merlini, G. [2 ]
Rapezzi, C. [1 ]
机构：
[1] Inst Cardiol, Bologna, Italy
[2] IRCCS San Matteo, Ctr Amyloidosis, Biotechnol Labs, Pavia, Italy
[3] Careggi Univ Hosp, Florence, Italy
来源：
EUROPEAN HEART JOURNAL | 2012年 / 33卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：365 / 365
页数：1
相关论文
共 50 条
  • [1] Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective
    Rapezzi, Claudio
    Quarta, Candida Cristina
    Obici, Laura
    Perfetto, Federico
    Longhi, Simone
    Salvi, Fabrizio
    Biagini, Elena
    Lorenzini, Massimiliano
    Grigioni, Francesco
    Leone, Ornella
    Cappelli, Francesco
    Palladini, Giovanni
    Rimessi, Paola
    Ferlini, Alessandra
    Arpesella, Giorgio
    Pinna, Antonio Daniele
    Merlini, Giampaolo
    Perlini, Stefano
    EUROPEAN HEART JOURNAL, 2013, 34 (07) : 520 - 528
  • [2] Hereditary transthyretin-related amyloidosis with exclusive cardiac phenotype
    Ciliberti, P.
    Quarta, C. C.
    Riva, L.
    Longhi, S.
    Galati, G.
    Villani, C.
    Salvi, F.
    Lorenzini, M.
    Branzi, A.
    Rapezzi, C.
    EUROPEAN HEART JOURNAL, 2009, 30 : 539 - 539
  • [3] Non-invasive identification of senile systemic amyloidosis and mutant transthyretin-related amyloidosis with exclusively cardiac phenotype by 99mTc-DPD scintigraphy
    Quarta, C.
    Longhi, S.
    Gagliardi, C.
    Gallo, P.
    Guidalotti, P. L.
    Pettinato, C.
    Bonfiglioli, R.
    Leone, O.
    Villani, C.
    Rapezzi, C.
    EUROPEAN HEART JOURNAL, 2011, 32 : 185 - 185
  • [4] Diagnosis and treatment of transthyretin-related amyloidosis cardiomyopathy
    Teng, Catherine
    Li, Pengyang
    Bae, Ju Young
    Pan, Su
    Dixon, Richard A. F.
    Liu, Qi
    CLINICAL CARDIOLOGY, 2020, 43 (11) : 1223 - 1231
  • [5] Hereditary transthyretin-related amyloidosis
    Finsterer, Josef
    Iglseder, Stephan
    Wanschitz, Julia
    Topakian, Raffi
    Loscher, Wolfgang N.
    Grisold, Wolfgang
    ACTA NEUROLOGICA SCANDINAVICA, 2019, 139 (02): : 92 - 105
  • [6] Noninvasive diagnosis of hereditary transthyretin-related cardiac amyloidosis A case report
    Qin, Jin
    Zhan, Chenao
    Li, Haojie
    Han, Yunfeng
    Wang, Hong
    Li, Rui
    Ma, Fei
    Yan, Jiangtao
    MEDICINE, 2019, 98 (30)
  • [7] Early Identification of Transthyretin-Related Hereditary Cardiac Amyloidosis
    Arbustini, Eloisa
    Merlini, Giampaolo
    JACC-CARDIOVASCULAR IMAGING, 2014, 7 (05) : 511 - 514
  • [8] Hereditary Transthyretin-Related Amyloidosis With Predominant or Exclusive Cardiac Phenotype in a White Caucasian Population
    Ciliberti, Paolo
    Quarta, Candida Cristina
    Riva, Letizia
    Longhi, Simone
    Salvi, Fabrizio
    Biagini, Elena
    Galati, Giuseppe
    Branzi, Angelo
    Rapezzi, Claudio
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 53 (10) : A168 - A168
  • [9] Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiology
    Skrahina, Volha
    Grittner, Ulrike
    Beetz, Christian
    Skripuletz, Thomas
    Juenemann, Martin
    Kraemer, Heidrun H.
    Hahn, Katrin
    Rieth, Andreas
    Schaechinger, Volker
    Patten, Monica
    Tanislav, Christian
    Achenbach, Stephan
    Assmus, Birgit
    Knebel, Fabian
    Gingele, Stefan
    Skrahin, Aliaksandr
    Hartkamp, Joerg
    Foerster, Toni M.
    Roesner, Sabine
    Pereira, Catarina
    Rolfs, Arndt
    ANNALS OF MEDICINE, 2021, 53 (01) : 1787 - 1796
  • [10] MOLECULAR STRATEGIES IN GENETIC DIAGNOSIS OF TRANSTHYRETIN-RELATED HEREDITARY AMYLOIDOSIS
    FERLINI, A
    FINI, S
    SALVI, F
    PATROSSO, MC
    VEZZONI, P
    FORABOSCO, A
    FASEB JOURNAL, 1992, 6 (10): : 2864 - 2866
12345