141 related articles for article (PubMed ID: 32269295)
21. Clinical and pathological studies of cardiac amyloidosis in transthyretin type familial amyloid polyneuropathy.
Hattori T; Takei Y; Koyama J; Nakazato M; Ikeda S
Amyloid; 2003 Dec; 10(4):229-39. PubMed ID: 14986482
[TBL] [Abstract][Full Text] [Related]
22. Long-term effects of liver transplantation on small-fiber dysfunction in Japanese transthyretin (ATTR) V30M hereditary amyloidosis with polyneuropathy (FAP).
Obayashi K; Ueda M; Yamashita T; Tasaki M; Izaki A; Yanagisawa Y; Masuda T; Misumi Y; Ando Y
Amyloid; 2017 Mar; 24(sup1):99. PubMed ID: 28434340
[No Abstract] [Full Text] [Related]
23. Transthyretin-related amyloidoses and the heart: a clinical overview.
Rapezzi C; Quarta CC; Riva L; Longhi S; Gallelli I; Lorenzini M; Ciliberti P; Biagini E; Salvi F; Branzi A
Nat Rev Cardiol; 2010 Jul; 7(7):398-408. PubMed ID: 20479782
[TBL] [Abstract][Full Text] [Related]
24. Extremely early onset hereditary ATTR amyloidosis with G47R (p.G67R) mutation.
Kobayashi Y; Sekijima Y; Ogawa Y; Kondo Y; Miyazaki D; Ikeda SI
Amyloid; 2016 Sep; 23(3):205-206. PubMed ID: 27206384
[No Abstract] [Full Text] [Related]
25. Epidemiology of variant transthyretin amyloidosis at a reference center in Argentina.
Saez MS; Aguirre MA; Pérez de Arenaza D; Sorroche P; Nucifora E; Posadas Martinez ML
Mol Genet Genomic Med; 2021 Nov; 9(11):e1812. PubMed ID: 34668655
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Gastrointestinal amyloidosis associated with transthyretin Phe64Ser mutation.
Naderi AS; Farsian FN; Igarashi P
Am J Med Sci; 2007 Sep; 334(3):219-21. PubMed ID: 17873539
[TBL] [Abstract][Full Text] [Related]
28. [Familial approach in hereditary transthyretin cardiac amyloidosis].
García-Pavía P; Avellana P; Bornstein B; Heine-Suñer D; Cobo-Marcos M; Gómez-Bueno M; Segovia J; Alonso-Pulpón LA
Rev Esp Cardiol; 2011 Jun; 64(6):523-6. PubMed ID: 21439703
[TBL] [Abstract][Full Text] [Related]
29. Hereditary amyloidosis with cardiomyopathy caused by the novel variant transthyretin A36D.
Yamashita T; Ueda M; Saga N; Nanto K; Tasaki M; Masuda T; Misumi Y; Oda S; Fujimoto A; Amano T; Takamatsu K; Yamashita S; Obayashi K; Matsui H; Ando Y
Amyloid; 2016 Sep; 23(3):207-208. PubMed ID: 27646980
[No Abstract] [Full Text] [Related]
30. 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]
31. Cardiac amyloidosis associated with the transthyretin Ile122 mutation in a Caucasian family.
Hamidi Asl K; Nakamura M; Yamashita T; Benson MD
Amyloid; 2001 Dec; 8(4):263-9. PubMed ID: 11791619
[TBL] [Abstract][Full Text] [Related]
32. A new Arg54Gly transthyretin gene mutation associated with vitreous amyloidosis in Chinese.
Shi Y; Li J; Hu J; Hu J; Sun L; Li H; Shi R; Yang L; Sun Y; Li C
Eye Sci; 2011 Dec; 26(4):230-8. PubMed ID: 22187309
[TBL] [Abstract][Full Text] [Related]
33. Late onset cardiomyopathy as presenting sign of ATTR A45G amyloidosis caused by a novel TTR mutation (p.A65G).
Klaassen SHC; Lemmink HH; Bijzet J; Glaudemans AWJM; Bos R; Plattel W; van den Berg MP; Slart RHJA; Nienhuis HLA; van Veldhuisen DJ; Hazenberg BPC
Cardiovasc Pathol; 2017; 29():19-22. PubMed ID: 28460244
[TBL] [Abstract][Full Text] [Related]
34. Heart transplantation for homozygous familial transthyretin (TTR) V122I cardiac amyloidosis.
Hamour IM; Lachmann HJ; Goodman HJ; Petrou M; Burke MM; Hawkins PN; Banner NR
Am J Transplant; 2008 May; 8(5):1056-9. PubMed ID: 18318779
[TBL] [Abstract][Full Text] [Related]
35. Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey).
Maurer MS; Hanna M; Grogan M; Dispenzieri A; Witteles R; Drachman B; Judge DP; Lenihan DJ; Gottlieb SS; Shah SJ; Steidley DE; Ventura H; Murali S; Silver MA; Jacoby D; Fedson S; Hummel SL; Kristen AV; Damy T; Planté-Bordeneuve V; Coelho T; Mundayat R; Suhr OB; Waddington Cruz M; Rapezzi C;
J Am Coll Cardiol; 2016 Jul; 68(2):161-72. PubMed ID: 27386769
[TBL] [Abstract][Full Text] [Related]
36. Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis.
Ihse E; Ybo A; Suhr O; Lindqvist P; Backman C; Westermark P
J Pathol; 2008 Oct; 216(2):253-61. PubMed ID: 18729067
[TBL] [Abstract][Full Text] [Related]
37. Amyloid Cardiomyopathy in the Rare Transthyretin Tyr78Phe Mutation.
Tini G; Vianello PF; Gemelli C; Grandis M; Canepa M
J Cardiovasc Transl Res; 2019 Dec; 12(6):514-516. PubMed ID: 30604309
[TBL] [Abstract][Full Text] [Related]
38. A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.
Booth DR; Tan SY; Hawkins PN; Pepys MB; Frustaci A
Circulation; 1995 Feb; 91(4):962-7. PubMed ID: 7850982
[TBL] [Abstract][Full Text] [Related]
39. Familial amyloidosis in a large Spanish kindred resulting from a D38V mutation in the transthyretin gene.
Augustin S; Llige D; Andreu A; González A; Genescà J
Eur J Clin Invest; 2007 Aug; 37(8):673-8. PubMed ID: 17635579
[TBL] [Abstract][Full Text] [Related]
40. Cardiac findings and events observed in an open-label clinical trial of tafamidis in patients with non-Val30Met and non-Val122Ile hereditary transthyretin amyloidosis.
Damy T; Judge DP; Kristen AV; Berthet K; Li H; Aarts J
J Cardiovasc Transl Res; 2015 Mar; 8(2):117-27. PubMed ID: 25743445
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
