164 related articles for article (PubMed ID: 27646980)
1. 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]
2. 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]
3. 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]
4. A new ATTR Phe64Ile mutation with late-onset multiorgan involvement.
Tarquini R; Perfetto F; Bergesio F; Miliani A; Del Pace S; Frusconi S; Minuti B; Pelo E; Torricelli F
Amyloid; 2007 Dec; 14(4):289-92. PubMed ID: 17968689
[TBL] [Abstract][Full Text] [Related]
5. Highly selective leptomeningeal amyloidosis with transthyretin variant Ala25Thr.
Hagiwara K; Ochi H; Suzuki S; Shimizu Y; Tokuda T; Murai H; Shigeto H; Ohyagi Y; Iwata M; Iwaki T; Kira JI
Neurology; 2009 Apr; 72(15):1358-60. PubMed ID: 19365058
[No Abstract] [Full Text] [Related]
6. Familial amyloid cardiomyopathy masquerading as chronic Guillain-Barre syndrome: things are not always what they seem.
Hu D; Liu L; Yuan S; Yi Y; Peng D
Front Med; 2017 Jun; 11(2):293-296. PubMed ID: 28425041
[TBL] [Abstract][Full Text] [Related]
7. Heart failure and cardiac involvement as isolated manifestation of familial form of transthyretin amyloidosis resulting from Val30Met mutation with no clinical signs of polyneuropathy.
Christoph DC; Boese D; Johnson KT; Schlosser TW; Hunold P; Baba HA; Erbel R; Philipp S
Circ Heart Fail; 2009 Sep; 2(5):512-5. PubMed ID: 19808383
[No Abstract] [Full Text] [Related]
8. 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]
9. The pathologic spectrum of oculoleptomeningeal amyloidosis with Val30Gly transthyretin gene mutation in a postmortem case.
Martin SE; Benson MD; Hattab EM
Hum Pathol; 2014 May; 45(5):1105-8. PubMed ID: 24613567
[TBL] [Abstract][Full Text] [Related]
10. [Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. A clinical, genetic and echocardiographic study of an affected Danish family].
Svendsen IH; Steensgaard-Hansen F; Nordvåg BY
Ugeskr Laeger; 1999 Sep; 161(36):4995-9. PubMed ID: 10489791
[TBL] [Abstract][Full Text] [Related]
11. The first Caucasian patient with p.Val122Ile mutated-transthyretin cardiac amyloidosis treated with isolated heart transplantation.
Ammirati E; Marziliano N; Vittori C; Pedrotti P; Bramerio MA; Motta V; Orsini F; Veronese S; Merlini PA; Martinelli L; Frigerio M
Amyloid; 2012 Jun; 19(2):113-7. PubMed ID: 22449240
[TBL] [Abstract][Full Text] [Related]
12. Hereditary ATTR amyloidosis: a single-institution experience with 266 patients.
Swiecicki PL; Zhen DB; Mauermann ML; Kyle RA; Zeldenrust SR; Grogan M; Dispenzieri A; Gertz MA
Amyloid; 2015; 22(2):123-31. PubMed ID: 26017327
[TBL] [Abstract][Full Text] [Related]
13. Transthyretin Tyr69-to-Ile mutation (double-nucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome.
Takei Y; Hattori T; Yazaki M; Tokuda T; Urasawa N; Kanai S; Ikeda S
Amyloid; 2003 Mar; 10(1):25-8. PubMed ID: 12762138
[TBL] [Abstract][Full Text] [Related]
14. Direct tissue evaluation via immunofluorescence: in the diagnosis of hereditary transthyretin cardiac amyloidosis.
Fradley MG; Thakuria JV; Collins AB; Moore SA; Stone JR
Tex Heart Inst J; 2012; 39(1):71-5. PubMed ID: 22412233
[TBL] [Abstract][Full Text] [Related]
15. Amyloid fibril composition as a predictor of development of cardiomyopathy after liver transplantation for hereditary transthyretin amyloidosis.
Gustafsson S; Ihse E; Henein MY; Westermark P; Lindqvist P; Suhr OB
Transplantation; 2012 May; 93(10):1017-23. PubMed ID: 22395298
[TBL] [Abstract][Full Text] [Related]
16. Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis.
da Silva-Batista JA; Marques W; Oliveira MTJS; Lins LVC; Galvão AJP; Miguel DSCG; Machado-Costa MC
J Hum Genet; 2020 Aug; 65(8):711-713. PubMed ID: 32269295
[TBL] [Abstract][Full Text] [Related]
17. Transthyretin Cardiac Amyloidosis.
Mankad AK; Shah KB
Curr Cardiol Rep; 2017 Aug; 19(10):97. PubMed ID: 28840452
[TBL] [Abstract][Full Text] [Related]
18. Hereditary transthyretin amyloidosis: molecular basis and therapeutical strategies.
Saraiva MJ
Expert Rev Mol Med; 2002 May; 4(12):1-11. PubMed ID: 14987380
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. (99m)Tc-HMDP scintigraphy rectifies wrong diagnosis of AL amyloidosis.
Galat A; Van Der Gucht A; Colombat M; Attias D; Itti E; Meignan M; Lebras F; Molinier-Frenkel V; Benhaiem N; Guellich A; Rosso J; Damy T
J Nucl Cardiol; 2015 Aug; 22(4):853-7. PubMed ID: 26002815
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
