These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
224 related articles for article (PubMed ID: 34380564)
1. Established and candidate transthyretin amyloidosis variants identified in the Saudi population by data mining. Abouelhoda M; Mohty D; Alayary I; Meyer BF; Arold ST; Fadel BM; Monies D Hum Genomics; 2021 Aug; 15(1):52. PubMed ID: 34380564 [TBL] [Abstract][Full Text] [Related]
2. Diagnosis of genetic amyloidosis through the analysis of transthyretin gene mutation using high-resolution melting. Lahuerta C; Menao S; Gracia-Gutierrez A; Bueno-Juana E; Guillén N; Sorribas V; Gracia AA; Aibar MA Int J Cardiol; 2020 Feb; 301():220-225. PubMed ID: 31740141 [TBL] [Abstract][Full Text] [Related]
3. Genetic testing improves identification of transthyretin amyloid (ATTR) subtype in cardiac amyloidosis. Brown EE; Lee YZJ; Halushka MK; Steenbergen C; Johnson NM; Almansa J; Tedford RJ; Cingolani O; Russell SD; Sharma K; Judge DP Amyloid; 2017 Jun; 24(2):92-95. PubMed ID: 28494620 [TBL] [Abstract][Full Text] [Related]
5. Genetic and clinical characteristics of hereditary transthyretin amyloidosis in endemic and non-endemic areas: experience from a single-referral center in Japan. Yamashita T; Ueda M; Misumi Y; Masuda T; Nomura T; Tasaki M; Takamatsu K; Sasada K; Obayashi K; Matsui H; Ando Y J Neurol; 2018 Jan; 265(1):134-140. PubMed ID: 29177547 [TBL] [Abstract][Full Text] [Related]
6. THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis. Coelho T; Maurer MS; Suhr OB Curr Med Res Opin; 2013 Jan; 29(1):63-76. PubMed ID: 23193944 [TBL] [Abstract][Full Text] [Related]
7. Allele specific expression of the transthyretin gene in swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles. Norgren N; Hellman U; Ericzon BG; Olsson M; Suhr OB PLoS One; 2012; 7(11):e49981. PubMed ID: 23185504 [TBL] [Abstract][Full Text] [Related]
8. DISCOVERY: prevalence of transthyretin ( Akinboboye O; Shah K; Warner AL; Damy T; Taylor HA; Gollob J; Powell C; Karsten V; Vest J; Maurer MS Amyloid; 2020 Dec; 27(4):223-230. PubMed ID: 32456532 [TBL] [Abstract][Full Text] [Related]
9. Monoclonal gammopathy of undetermined significance in systemic transthyretin amyloidosis (ATTR). Phull P; Sanchorawala V; Connors LH; Doros G; Ruberg FL; Berk JL; Sarosiek S Amyloid; 2018 Mar; 25(1):62-67. PubMed ID: 29424556 [TBL] [Abstract][Full Text] [Related]
10. New sequence variants in patients affected by amyloidosis show transthyretin instability by isoelectric focusing. Hinderhofer K; Obermaier C; Hegenbart U; Schönland S; Seidler M; Sommer-Ort I; Barth U Amyloid; 2019 Jun; 26(2):85-93. PubMed ID: 31074293 [TBL] [Abstract][Full Text] [Related]
11. Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiology. Skrahina V; Grittner U; Beetz C; Skripuletz T; Juenemann M; Krämer HH; Hahn K; Rieth A; Schaechinger V; Patten M; Tanislav C; Achenbach S; Assmus B; Knebel F; Gingele S; Skrahin A; Hartkamp J; Förster TM; Roesner S; Pereira C; Rolfs A Ann Med; 2021 Dec; 53(1):1787-1796. PubMed ID: 34658264 [TBL] [Abstract][Full Text] [Related]
12. Origin of sporadic late-onset hereditary ATTR Val30Met amyloidosis in Japan. Ueda M; Yamashita T; Misumi Y; Masuda T; Ando Y Amyloid; 2018 Sep; 25(3):143-147. PubMed ID: 30486687 [TBL] [Abstract][Full Text] [Related]