141 related articles for article (PubMed ID: 32269295)
41. Liver Transplantation for Hereditary Transthyretin Amyloidosis: After 20 Years Still the Best Therapeutic Alternative?
Ericzon BG; Wilczek HE; Larsson M; Wijayatunga P; Stangou A; Pena JR; Furtado E; Barroso E; Daniel J; Samuel D; Adam R; Karam V; Poterucha J; Lewis D; Ferraz-Neto BH; Cruz MW; Munar-Ques M; Fabregat J; Ikeda S; Ando Y; Heaton N; Otto G; Suhr O
Transplantation; 2015 Sep; 99(9):1847-54. PubMed ID: 26308415
[TBL] [Abstract][Full Text] [Related]
42. Two siblings diagnosed to have transthyretin-related familial amyloid cardiomyopathy around the same time at different hospitals.
Miyamura M; Terasaki F; Ishibashi K; Shimazaki C; Kimura F; Kuwabara H; Tsuji M; Shibayama Y; Sekijima Y; Tojo K; Ishizaka N
Intern Med; 2012; 51(5):465-9. PubMed ID: 22382560
[TBL] [Abstract][Full Text] [Related]
43. Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloid.
Eriksson M; Büttner J; Todorov T; Yumlu S; Schönland S; Hegenbart U; Kristen AV; Dengler T; Lohse P; Helmke B; Schmidt H; Röcken C
Am J Surg Pathol; 2009 Jan; 33(1):58-65. PubMed ID: 18830126
[TBL] [Abstract][Full Text] [Related]
44. 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]
45. A case of cardiac amyloidosis in an elderly Japanese patient with amyloidogenic transthyretin Val122Ile variant.
Ono R; Takahashi H; Sato T; Yamazaki T; Hori Y; Fukushima K
J Cardiol Cases; 2020 Nov; 22(5):221-225. PubMed ID: 33133314
[TBL] [Abstract][Full Text] [Related]
46. Laboratory assessment of transthyretin amyloidosis.
Benson MD; Yazaki M; Magy N
Clin Chem Lab Med; 2002 Dec; 40(12):1262-5. PubMed ID: 12553428
[TBL] [Abstract][Full Text] [Related]
47. A transthyretin variant, Asp18Asn, associated with amyloid cardiomyopathy: a new African-American variant?
Quarta CC; Falk RH
Amyloid; 2012 Dec; 19(4):204-7. PubMed ID: 23126592
[TBL] [Abstract][Full Text] [Related]
48. Cysteine 10 is a key residue in amyloidogenesis of human transthyretin Val30Met.
Takaoka Y; Ohta M; Miyakawa K; Nakamura O; Suzuki M; Takahashi K; Yamamura K; Sakaki Y
Am J Pathol; 2004 Jan; 164(1):337-45. PubMed ID: 14695346
[TBL] [Abstract][Full Text] [Related]
49. Progression of cardiac amyloid deposition in hereditary transthyretin amyloidosis patients after liver transplantation.
Liepnieks JJ; Benson MD
Amyloid; 2007 Dec; 14(4):277-82. PubMed ID: 17968687
[TBL] [Abstract][Full Text] [Related]
50. A Danish kindred with familial amyloid cardiomyopathy revisited: identification of a mutant transthyretin-methionine111 variant in serum from patients and carriers.
Ranløv I; Alves IL; Ranløv PJ; Husby G; Costa PP; Saraiva MJ
Am J Med; 1992 Jul; 93(1):3-8. PubMed ID: 1626570
[TBL] [Abstract][Full Text] [Related]
51. Early onset aggressive hereditary amyloidosis: report of an Italian family with TTR Arg47 mutation.
Salvi F; Pastorelli F; Plasmati R; Ferlini A; Grazi GL; Jovine E; Mascalchi M; Tassinari CA
Neurol Sci; 2005 Jun; 26(2):140-2. PubMed ID: 15995833
[TBL] [Abstract][Full Text] [Related]
52. Tafamidis: A Review in Transthyretin Amyloidosis with Polyneuropathy.
Lamb YN; Deeks ED
Drugs; 2019 Jun; 79(8):863-874. PubMed ID: 31098895
[TBL] [Abstract][Full Text] [Related]
53. Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French family.
Magy N; Valleix S; Grateau G; Algros MP; Guillemain R; Kantelip B; Delpech M; Dupond JL
Amyloid; 2002 Dec; 9(4):272-5. PubMed ID: 12557758
[TBL] [Abstract][Full Text] [Related]
54. Novel methods for detecting amyloidogenic proteins in transthyretin related amyloidosis.
Ando Y; Ueda M
Front Biosci; 2008 May; 13():5548-58. PubMed ID: 18508604
[TBL] [Abstract][Full Text] [Related]
55. Liver transplantation for hereditary transthyretin amyloidosis.
Suhr OB; Herlenius G; Friman S; Ericzon BG
Liver Transpl; 2000 May; 6(3):263-76. PubMed ID: 10827225
[TBL] [Abstract][Full Text] [Related]
56. Association between a point mutation at the -743-bp region of the transthyretin (TTR) gene and familial vitreous amyloidosis.
Nie XM; Cai SJ; Xie B; Chen XW; Jiang M
Genet Mol Res; 2016 Mar; 15(1):. PubMed ID: 27051017
[TBL] [Abstract][Full Text] [Related]
57. A novel compound heterozygote (FAP ATTR Arg104His/ATTR Val30Met) with high serum transthyretin (TTR) and retinol binding protein (RBP) levels.
Terazaki H; Ando Y; Misumi S; Nakamura M; Ando E; Matsunaga N; Shoji S; Okuyama M; Ideta H; Nakagawa K; Ishizaki T; Ando M; Saraiva MJ
Biochem Biophys Res Commun; 1999 Oct; 264(2):365-70. PubMed ID: 10529370
[TBL] [Abstract][Full Text] [Related]
58. Role of (99m)Tc-DPD scintigraphy in diagnosis and prognosis of hereditary transthyretin-related cardiac amyloidosis.
Rapezzi C; Quarta CC; Guidalotti PL; Pettinato C; Fanti S; Leone O; Ferlini A; Longhi S; Lorenzini M; Reggiani LB; Gagliardi C; Gallo P; Villani C; Salvi F
JACC Cardiovasc Imaging; 2011 Jun; 4(6):659-70. PubMed ID: 21679902
[TBL] [Abstract][Full Text] [Related]
59. Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant.
Sattianayagam PT; Hahn AF; Whelan CJ; Gibbs SD; Pinney JH; Stangou AJ; Rowczenio D; Pflugfelder PW; Fox Z; Lachmann HJ; Wechalekar AD; Hawkins PN; Gillmore JD
Eur Heart J; 2012 May; 33(9):1120-7. PubMed ID: 21992998
[TBL] [Abstract][Full Text] [Related]
60. Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.
Tanaka M; Hirai S; Matsubara E; Okamoto K; Morimatsu M; Nakazato M
J Neurol Neurosurg Psychiatry; 1988 Apr; 51(4):576-8. PubMed ID: 3379433
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
