169 related articles for article (PubMed ID: 22187309)
1. 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]
2. Ophthalmic manifestations in a Chinese family with familial amyloid polyneuropathy due to a TTR Gly83Arg mutation.
Liu T; Zhang B; Jin X; Wang W; Lee J; Li J; Yuan H; Cheng X
Eye (Lond); 2014 Jan; 28(1):26-33. PubMed ID: 24113303
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [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]
5. Transthyretin Ala36Pro mutation in a Chinese pedigree of familial transthyretin amyloidosis with elevated vitreous and serum vascular endothelial growth factor.
Zou X; Dong F; Zhang S; Tian R; Sui R
Exp Eye Res; 2013 May; 110():44-9. PubMed ID: 23438977
[TBL] [Abstract][Full Text] [Related]
6. A mouse model of a novel missense mutation (Gly83Arg) in a Chinese kindred manifesting vitreous amyloidosis only.
Ran LX; Zheng ZY; Xie B; Nie XM; Chen XW; Su G; Cai SJ
Exp Eye Res; 2018 Apr; 169():13-19. PubMed ID: 29360446
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Transthyretin-related hereditary amyloidosis in a Chinese family with TTR Y114C mutation.
Zhang Y; Deng YL; Ma JF; Zheng L; Hong Z; Wang ZQ; Sheng CY; Xiao Q; Cao L; Chen SD
Neurodegener Dis; 2011; 8(4):187-93. PubMed ID: 21135536
[TBL] [Abstract][Full Text] [Related]
9. Vitreous amyloidosis in two large mainland Chinese kindreds resulting from transthyretin variant Lys35Thr and Leu55Arg.
Long D; Zeng J; Wu LQ; Tang LS; Wang HL; Wang H
Ophthalmic Genet; 2012 Mar; 33(1):28-33. PubMed ID: 21843040
[TBL] [Abstract][Full Text] [Related]
10. A novel transthyretin Lys70Glu (p.Lys90Glu) mutation presenting with vitreous amyloidosis and carpal tunnel syndrome.
Raivio VE; Jonasson J; Myllykangas L; Ala-Mello S; Kankuri-Tammilehto M; Kiuru-Enari S; Westermark P; Tanskanen M; Kivelä T
Amyloid; 2016; 23(1):46-50. PubMed ID: 26828956
[TBL] [Abstract][Full Text] [Related]
11. Clinical and hereditary features of familial vitreous amyloidosis in Chinese.
Shi Y; Yang L; Li J; Hu J; Shi R; Sun Y; Zhang C
Eye Sci; 2011 Mar; 26(1):52-5. PubMed ID: 21425497
[TBL] [Abstract][Full Text] [Related]
12. Vitreous Amyloidosis: Ocular, Systemic, and Genetic Insights.
Venkatesh P; Selvan H; Singh SB; Gupta D; Kashyap S; Temkar S; Gogia V; Tripathy K; Chawla R; Vohra R
Ophthalmology; 2017 Jul; 124(7):1014-1022. PubMed ID: 28412068
[TBL] [Abstract][Full Text] [Related]
13. Familial vitreous amyloidosis resulting from transthyretin variant Gly83Arg.
Xie B; Cai SJ; Jiang M; Li H; Su G
Acta Ophthalmol; 2017 Sep; 95(6):e520-e521. PubMed ID: 28266151
[No Abstract] [Full Text] [Related]
14. [Transthyretin Arg-83 mutation in vitreous amyloidosis].
Chen L; Lü L; Zhang P; Li Y; Lin J
Yan Ke Xue Bao; 2008 Mar; 24(1):65-7. PubMed ID: 18709962
[TBL] [Abstract][Full Text] [Related]
15. Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His.
Blevins G; Macaulay R; Harder S; Fladeland D; Yamashita T; Yazaki M; Hamidi Asl K; Benson MD; Donat JR
Neurology; 2003 May; 60(10):1625-30. PubMed ID: 12771253
[TBL] [Abstract][Full Text] [Related]
16. A severe form of amyloidotic polyneuropathy in a Costa Rican family with a rare transthyretin mutation (Glu54Lys).
Busse A; Sánchez MA; Monterroso V; Alvarado MV; León P
Am J Med Genet A; 2004 Jul; 128A(2):190-4. PubMed ID: 15214015
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Identification of a novel transthyretin Thr59Lys/Arg104His. A case of compound heterozygosity in a Chinese patient diagnosed with familial transthyretin amyloidosis.
Lim A; Prokaeva T; Connor LH; Falk RH; Skinner M; Costello CE
Amyloid; 2002 Jun; 9(2):134-40. PubMed ID: 12440486
[TBL] [Abstract][Full Text] [Related]
20. Hereditary Transthyretin Amyloidosis in Eight Chinese Families.
Meng LC; Lyu H; Zhang W; Liu J; Wang ZX; Yuan Y
Chin Med J (Engl); 2015 Nov; 128(21):2902-5. PubMed ID: 26521788
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
