These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
146 related articles for article (PubMed ID: 34483316)
1. OCULAR MANIFESTATIONS OF ASP38ALA AND THR59LYS FAMILIAL TRANSTHYRETIN AMYLOIDOSIS. Choi KJ; Son KY; Kang SW; Kim D; Choi JO; Kim HJ; Kim JS; Jeon ES; Kim AY; Kang MC; Kim SJ Retina; 2022 Feb; 42(2):396-403. PubMed ID: 34483316 [TBL] [Abstract][Full Text] [Related]
2. 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]
7. 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]
8. Ocular Involvement in Hereditary Transthyretin Amyloidosis: A Case Series Describing Novel Potential Biomarkers. Minnella AM; Rissotto R; Maceroni M; Romano A; Fasciani R; Luigetti M; Sabatelli M; Rizzo S; Falsini B Genes (Basel); 2021 Jun; 12(6):. PubMed ID: 34207092 [TBL] [Abstract][Full Text] [Related]
9. Multimodal retinal imaging in a Chinese kindred with familial amyloid polyneuropathy secondary to transthyretin Ile107Met mutation. Lv W; Chen J; Chen W; Hou P; Pang CP; Chen H Eye (Lond); 2014 Apr; 28(4):452-8. PubMed ID: 24480837 [TBL] [Abstract][Full Text] [Related]
10. Conjunctival lymphangiectasia as a biomarker of severe systemic disease in Ser77Tyr hereditary transthyretin amyloidosis. Bunod R; Adams D; Cauquil C; Francou B; Labeyrie C; Bourenane H; Adam C; Algalarrondo V; Slama M; Darce-Bello M; Barreau E; Labetoulle M; Rousseau A Br J Ophthalmol; 2020 Oct; 104(10):1363-1367. PubMed ID: 31949094 [TBL] [Abstract][Full Text] [Related]
11. Ocular amyloid angiopathy associated with familial amyloidotic polyneuropathy caused by amyloidogenic transthyretin Y114C. Kawaji T; Ando Y; Nakamura M; Yamashita T; Wakita M; Ando E; Hirata A; Tanihara H Ophthalmology; 2005 Dec; 112(12):2212. PubMed ID: 16225929 [TBL] [Abstract][Full Text] [Related]
12. Solar Eruption in Hereditary Transthyretin Amyloidosis. Rousseau A; Bodaghi B; Labetoulle M Ophthalmology; 2019 Mar; 126(3):371. PubMed ID: 30803513 [No Abstract] [Full Text] [Related]
13. Ophthalmological manifestations in hereditary transthyretin (ATTR V30M) carriers: a review of 513 cases. Beirão JM; Malheiro J; Lemos C; Beirão I; Costa P; Torres P Amyloid; 2015; 22(2):117-22. PubMed ID: 26096568 [TBL] [Abstract][Full Text] [Related]
14. OCULAR ANGIOGRAPHIC FEATURES IN JAPANESE PATIENTS WITH VAL30MET HEREDITARY TRANSTHYRETIN AMYLOIDOSIS. Kakihara S; Hirano T; Kitahara J; Matsuda Y; Imai A; Miyahara T; Murata T Retina; 2022 Jan; 42(1):210-215. PubMed ID: 34483312 [TBL] [Abstract][Full Text] [Related]
15. AN 82-YEAR-OLD WOMAN WITH RETINAL VASCULAR SHEATHING AND VITREOUS HEMORRHAGE. Hudson JL; Schwartz SG; Davis JL Retin Cases Brief Rep; 2023 Jun; 17(4S):S36-S40. PubMed ID: 35993733 [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. Ophthalmological manifestations of hereditary transthyretin amyloidosis. Gondim FAA; Holanda Filha JG; Moraes Filho MO Arq Bras Oftalmol; 2022; 85(5):528-538. PubMed ID: 35417510 [TBL] [Abstract][Full Text] [Related]
19. BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 Gene. Toto L; Boon CJ; Di Antonio L; Battaglia Parodi M; Mastropasqua R; Antonucci I; Stuppia L; Mastropasqua L Retina; 2016 Aug; 36(8):1586-95. PubMed ID: 26716959 [TBL] [Abstract][Full Text] [Related]
20. Ocular Involvement in Hereditary Amyloidosis. Minnella AM; Rissotto R; Antoniazzi E; Di Girolamo M; Luigetti M; Maceroni M; Bacherini D; Falsini B; Rizzo S; Obici L Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34206500 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]