95 related articles for article (PubMed ID: 20143571)
21. [Identification of a TTR gene mutation in a family with hereditary vitreous amyloidosis].
Xie Y; Zhao Y; Zhou JJ; Wang X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb; 29(1):13-5. PubMed ID: 22311483
[TBL] [Abstract][Full Text] [Related]
22. New transthyretin variants SER 91 and SER 116 associated with familial amyloidotic polyneuropathy. Mutations in brief no. 151. Online.
Misrahi AM; Plante V; Lalu T; Serre L; Adams D; Lacroix DC; Saïd G
Hum Mutat; 1998; 12(1):71. PubMed ID: 10627135
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Risk of transmission of systemic transthyretin amyloidosis after domino liver transplantation.
Lladó L; Baliellas C; Casasnovas C; Ferrer I; Fabregat J; Ramos E; Castellote J; Torras J; Xiol X; Rafecas A
Liver Transpl; 2010 Dec; 16(12):1386-92. PubMed ID: 21117248
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. Oculoleptomeningeal amyloidosis in a patient with a TTR Val30Gly mutation in the transthyretin gene.
Roe RH; Fisher Y; Eagle RC; Fine HF; Cunningham ET
Ophthalmology; 2007 Nov; 114(11):e33-7. PubMed ID: 17980738
[TBL] [Abstract][Full Text] [Related]
28. [An autopsy case of leptomeningeal amyloidosis associated with transthyretin Gly47Arg mutation].
Uehara T; Kakuda K; Sumi-Akamaru H; Yamauchi A; Mochizuki H; Naka T
Rinsho Shinkeigaku; 2016 Nov; 56(11):777-780. PubMed ID: 27784877
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Familial amyloid polyneuropathy related to transthyretin Gly42 in a Japanese family.
Uemichi T; Ueno S; Fujimura H; Umekage T; Yorifuji S; Matsuzawa Y; Tarui S
Muscle Nerve; 1992 Aug; 15(8):904-11. PubMed ID: 1353861
[TBL] [Abstract][Full Text] [Related]
31. Clinical and histopathological features of progressive-type familial amyloidotic polyneuropathy with TTR Lys54.
Nagasaka T; Togashi S; Watanabe H; Iida H; Nagasaka K; Nakamura Y; Miwa M; Kobayashi F; Shindo K; Shiozawa Z
J Neurol Sci; 2009 Jan; 276(1-2):88-94. PubMed ID: 18930252
[TBL] [Abstract][Full Text] [Related]
32. Mutation p.G83R in the transthyretin gene is associated with hereditary vitreous amyloidosis in Han Chinese families.
Zhang AM; Wang H; Sun P; Hu QX; He Y; Yao YG
Mol Vis; 2013; 19():1631-8. PubMed ID: 23901247
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.
Magy N; Liepnieks JJ; Gil H; Kantelip B; Dupond JL; Kluve-Beckerman B; Benson MD
Amyloid; 2003 Mar; 10(1):29-33. PubMed ID: 12762139
[TBL] [Abstract][Full Text] [Related]
35. [Amyloidosis of the vitreous body. Possibilities of diagnosis].
Soltau JB; Seiberth V; Knorz MC; Liesenhoff H
Fortschr Ophthalmol; 1991; 88(4):408-10. PubMed ID: 1786932
[TBL] [Abstract][Full Text] [Related]
36. [Cerebral amyloid angiopathy with familial transthyretin-derived oculoleptomeningeal amyloidosis].
Ikeda SI
Brain Nerve; 2013 Jul; 65(7):831-42. PubMed ID: 23832986
[TBL] [Abstract][Full Text] [Related]
37. Biochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis.
Mitsuhashi S; Yazaki M; Tokuda T; Sekijima Y; Washimi Y; Shimizu Y; Ando Y; Benson MD; Ikeda S
Amyloid; 2005 Dec; 12(4):216-25. PubMed ID: 16399646
[TBL] [Abstract][Full Text] [Related]
38. Analysis of transthyretin in human serum by capillary zone electrophoresis electrospray ionization time-of-flight mass spectrometry. Application to familial amyloidotic polyneuropathy type I.
Pont L; Benavente F; Barbosa J; Sanz-Nebot V
Electrophoresis; 2015 Jun; 36(11-12):1265-73. PubMed ID: 25820240
[TBL] [Abstract][Full Text] [Related]
39. Identification of a novel TTR Gly67Glu mutant and the first case series of familial transthyretin amyloidosis in Hong Kong Chinese.
Mak CM; Kwong YL; Lam CW; Chan SC; Lo CM; Fan ST; Chang CM; Lau YK; U LS; Tam S
Amyloid; 2007 Dec; 14(4):293-7. PubMed ID: 17968690
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]