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5. Transthyretin Ile 122 and cardiac amyloidosis in African-Americans. 2 case reports. Jacobson DR; Ittmann M; Buxbaum JN; Wieczorek R; Gorevic PD Tex Heart Inst J; 1997; 24(1):45-52. PubMed ID: 9068139 [TBL] [Abstract][Full Text] [Related]
6. Mutant Thr95Ile Transthyretin-Related Cardiac Amyloidosis With Polyneuropathy. Kim K; Oh J; Lee ST; Shim HS; Kang SM Circ J; 2019 Oct; 83(11):2328. PubMed ID: 31243187 [No Abstract] [Full Text] [Related]
7. [Cardiac manifestations of amyloidosis by deposits of transthyretin and apolipoprotein A1. Report of 3 families]. Lafitte S; Lafitte M; Perron JM; Ennouchi D; Vital C; Roudaut R Arch Mal Coeur Vaiss; 2003 Jun; 96(6):631-5. PubMed ID: 12868344 [TBL] [Abstract][Full Text] [Related]
8. Significance of the amyloidogenic transthyretin Val 122 Ile allele in African Americans in the Arteriosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) Studies. Buxbaum J; Alexander A; Koziol J; Tagoe C; Fox E; Kitzman D Am Heart J; 2010 May; 159(5):864-70. PubMed ID: 20435197 [TBL] [Abstract][Full Text] [Related]
9. Pressure-volume relationships in patients with transthyretin (ATTR) cardiac amyloidosis secondary to V122I mutations and wild-type transthyretin: Transthyretin Cardiac Amyloid Study (TRACS). Bhuiyan T; Helmke S; Patel AR; Ruberg FL; Packman J; Cheung K; Grogan D; Maurer MS Circ Heart Fail; 2011 Mar; 4(2):121-8. PubMed ID: 21191093 [TBL] [Abstract][Full Text] [Related]
10. Cardiac positron-emission tomography images with an amyloid-specific tracer in familial transthyretin-related systemic amyloidosis. Furukawa K; Ikeda S; Okamura N; Tashiro M; Tomita N; Furumoto S; Iwata R; Yanai K; Kudo Y; Arai H Circulation; 2012 Jan; 125(3):556-7. PubMed ID: 22271849 [No Abstract] [Full Text] [Related]
11. Identification of Transthyretin Cardiac Amyloidosis Using Serum Retinol-Binding Protein 4 and a Clinical Prediction Model. Arvanitis M; Koch CM; Chan GG; Torres-Arancivia C; LaValley MP; Jacobson DR; Berk JL; Connors LH; Ruberg FL JAMA Cardiol; 2017 Mar; 2(3):305-313. PubMed ID: 28196196 [TBL] [Abstract][Full Text] [Related]
12. Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS). Ruberg FL; Maurer MS; Judge DP; Zeldenrust S; Skinner M; Kim AY; Falk RH; Cheung KN; Patel AR; Pano A; Packman J; Grogan DR Am Heart J; 2012 Aug; 164(2):222-228.e1. PubMed ID: 22877808 [TBL] [Abstract][Full Text] [Related]
13. Early Detection of Cardiac Amyloidosis in Transthyretin Mutation Carriers. Nagano N; Muranaka A; Nishikawa R; Ohwada W; Kouzu H; Kamiyama N; Fujito T; Mochizuki A; Nagahara D; Nakanishi M; Ohkubo Y; Hisahara S; Nakao S; Katoh N; Ishikawa A; Sakurai A; Yano T Int Heart J; 2022; 63(1):168-175. PubMed ID: 35095067 [TBL] [Abstract][Full Text] [Related]
14. Usefulness of Combining Electrocardiographic and Echocardiographic Findings and Brain Natriuretic Peptide in Early Detection of Cardiac Amyloidosis in Subjects With Transthyretin Gene Mutation. Di Bella G; Minutoli F; Piaggi P; Casale M; Mazzeo A; Zito C; Oreto G; Baldari S; Vita G; Pingitore A; Khandheria BK; Carerj S Am J Cardiol; 2015 Oct; 116(7):1122-7. PubMed ID: 26253999 [TBL] [Abstract][Full Text] [Related]
15. Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans. Jacobson DR; Pastore RD; Yaghoubian R; Kane I; Gallo G; Buck FS; Buxbaum JN N Engl J Med; 1997 Feb; 336(7):466-73. PubMed ID: 9017939 [TBL] [Abstract][Full Text] [Related]
16. Diagnosis of cardiac amyloidosis by magnetic resonance imaging due to a new mutation in the transthyretin gene. Damy T; Plante-Bordeneuve V; Valleix S Arch Cardiovasc Dis; 2012 Nov; 105(11):614-5. PubMed ID: 23177490 [No Abstract] [Full Text] [Related]
17. Progression of ventricular wall thickening after liver transplantation for familial amyloidosis. Dubrey SW; Davidoff R; Skinner M; Bergethon P; Lewis D; Falk RH Transplantation; 1997 Jul; 64(1):74-80. PubMed ID: 9233704 [TBL] [Abstract][Full Text] [Related]
18. Can echocardiography and ECG discriminate hereditary transthyretin V30M amyloidosis from hypertrophic cardiomyopathy? Gustavsson S; Granåsen G; Grönlund C; Wiklund U; Mörner S; Henein M; Suhr OB; Lindqvist P Amyloid; 2015; 22(3):163-70. PubMed ID: 26104852 [TBL] [Abstract][Full Text] [Related]
19. Homozygous transthyretin mutation in an African American Male. Jacob EK; Edwards WD; Zucker M; D'Cruz C; Seshan SV; Crow FW; Highsmith WE J Mol Diagn; 2007 Feb; 9(1):127-31. PubMed ID: 17251346 [TBL] [Abstract][Full Text] [Related]
20. Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report. Yamamoto H; Hashimoto T; Kawamura S; Hiroe M; Yamashita T; Ando Y; Yokochi T J Med Case Rep; 2018 Dec; 12(1):370. PubMed ID: 30553273 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]