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Quoted phrase not found in phrase index: "Amyloid deposition in the vitreous humor"
Page 1
Recurrence of vitreous amyloidosis and need of surgical reintervention in Portuguese patients with familial amyloidosis ATTR V30M.
Beirão NM, Matos E, Beirão I, Costa PP, Torres P. Beirão NM, et al. Retina. 2011 Jul-Aug;31(7):1373-7. doi: 10.1097/IAE.0b013e318203c0c2. Retina. 2011. PMID: 21358362
An extensive, as possible, vitrectomy with indentation was performed in 41 eyes (complete), and in the others 13 eyes only a vitrectomy without indentation (incomplete) was performed. The parameters evaluated were the incidence of amyloid deposits and visual outcome …
An extensive, as possible, vitrectomy with indentation was performed in 41 eyes (complete), and in the others 13 eyes only a vitrectomy with …
RE-INTERVENTION IN DE NOVO VITREOUS OPACITIES AFTER PARS PLANA VITRECTOMY IN FAMILIAL AMYLOIDOTIC POLYNEUROPATHY TTR VAL30METPORTUGUESE PATIENTS.
Ferreira NN, Cunha Dias DA, Afonso Carvalho RP, Pardal Monteiro Coelho MT. Ferreira NN, et al. Retin Cases Brief Rep. 2019 Summer;13(3):273-278. doi: 10.1097/ICB.0000000000000578. Retin Cases Brief Rep. 2019. PMID: 28333852
After re-intervention, no further recurrence was observed (average follow-up of 10 months). CONCLUSION: De novo vitreous amyloid opacities may occur several years after pars plana vitrectomy. Amyloid deposition in vitreous cavity was o …
After re-intervention, no further recurrence was observed (average follow-up of 10 months). CONCLUSION: De novo vitreous am …
Ocular manifestations in liver transplant recipients with familial amyloid polyneuropathy.
Sandgren O, Kjellgren D, Suhr OB. Sandgren O, et al. Acta Ophthalmol. 2008 Aug;86(5):520-4. doi: 10.1111/j.1600-0420.2007.01098.x. Epub 2008 Apr 24. Acta Ophthalmol. 2008. PMID: 18435819 Free article.
PURPOSE: To evaluate postoperative ocular involvement in Swedish liver transplant (LT) recipients with familial amyloid polyneuropathy (FAP). METHODS: Routine ophthalmological examinations were performed in 48 LT recipients, with particular attention given to amyloid …
PURPOSE: To evaluate postoperative ocular involvement in Swedish liver transplant (LT) recipients with familial amyloid polyneuropath …
Vitreous involvement as initial presentation of hereditary transthyretin amyloidosis related to the rare TTR Ile107Met (p.Ile127Met) pathogenic variant.
Treviño-Herrera AB, Bustamante-Vargas AP, Lisker-Cervantes A, Ríos Y Valles Valles D, Villanueva-Mendoza C, González-Duarte A, Concha-Del-Río LE. Treviño-Herrera AB, et al. Ophthalmic Genet. 2022 Jun;43(3):413-419. doi: 10.1080/13816810.2022.2025606. Epub 2022 Jan 17. Ophthalmic Genet. 2022. PMID: 35038954
BACKGROUND: Hereditary transthyretin amyloidosis (ATTR) is a multisystemic disease with autosomal dominant inheritance, characterized by the deposition of amyloid-insoluble proteins. We describe a case of vitreous amyloidosis as the initial presentation of AT …
BACKGROUND: Hereditary transthyretin amyloidosis (ATTR) is a multisystemic disease with autosomal dominant inheritance, characterized by the …
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. Zhang AM, et al. Mol Vis. 2013 Jul 25;19:1631-8. Print 2013. Mol Vis. 2013. PMID: 23901247 Free PMC article.
PURPOSE: Hereditary vitreous amyloidosis (HVA) is a genetic ophthalmological disorder. ...A comprehensive medical examination of the patients showed no signs of abnormality except ophthalmologic symptoms, in which floccular turbidity and high echo in both vitreous b …
PURPOSE: Hereditary vitreous amyloidosis (HVA) is a genetic ophthalmological disorder. ...A comprehensive medical examination of the …
Transthyretin-related TTR hereditary amyloidosis of the vitreous body. Clinical and molecular characterization in two Italian families.
Salvi F, Salvi G, Volpe R, Mencucci R, Plasmati R, Michelucci R, Gobbi P, Santangelo M, Ferlini A, Forabosco A, et al. Salvi F, et al. Ophthalmic Paediatr Genet. 1993 Mar;14(1):9-16. doi: 10.3109/13816819309087617. Ophthalmic Paediatr Genet. 1993. PMID: 8345958
Molecular genetic characterization demonstrated different mutations of the transthyretin gene. In all patients belonging to the TTR Ala 49 family the vitreous body, the heart and the peripheral nervous system were massively infiltrated by amyloid matter. ...T …
Molecular genetic characterization demonstrated different mutations of the transthyretin gene. In all patients belonging to the TTR Ala 49 f …
Manifestations of transthyretin-related familial amyloidotic polyneuropathy: long-term follow-up of Japanese patients after liver transplantation.
Ohya Y, Okamoto S, Tasaki M, Ueda M, Jono H, Obayashi K, Takeda K, Okajima H, Asonuma K, Hara R, Tanihara H, Ando Y, Inomata Y. Ohya Y, et al. Surg Today. 2011 Sep;41(9):1211-8. doi: 10.1007/s00595-010-4488-5. Epub 2011 Aug 26. Surg Today. 2011. PMID: 21874417
PURPOSE: To observe which symptoms of transthyretin-related familial amyloidotic polyneuropathy (FAP) progressed in the long term after liver transplantation (LT), focusing on cardiac, kidney, and ocular symptoms. ...Progression of ocular amyloidosis was seen in 17 (50%) p …
PURPOSE: To observe which symptoms of transthyretin-related familial amyloidotic polyneuropathy (FAP) progressed in the long term aft …
Advanced glycation end product in familial amyloidotic polyneuropathy (FAP).
Nyhlin N, Ando Y, Nagai R, Suhr O, El Sahly M, Terazaki H, Yamashita T, Ando M, Horiuchi S. Nyhlin N, et al. J Intern Med. 2000 Apr;247(4):485-92. doi: 10.1046/j.1365-2796.2000.00668.x. J Intern Med. 2000. PMID: 10792563 Free article.
For amyloid preparation, vitreous samples from three FAP patients were used. ...Western blotting of purified amyloid from the vitreous body of FAP patients revealed a significant association of AGE with amyloid fibrils. ...
For amyloid preparation, vitreous samples from three FAP patients were used. ...Western blotting of purified amyloid fr …
The pathologic spectrum of oculoleptomeningeal amyloidosis with Val30Gly transthyretin gene mutation in a postmortem case.
Martin SE, Benson MD, Hattab EM. Martin SE, et al. Hum Pathol. 2014 May;45(5):1105-8. doi: 10.1016/j.humpath.2013.10.037. Epub 2014 Jan 2. Hum Pathol. 2014. PMID: 24613567
Unlike other forms of hereditary amyloidosis, this rare type displays amyloid deposition predominantly in the eyes and central nervous system. ...Subependymal amyloid deposits projecting into the lateral ventricles as well as amyloid depositi …
Unlike other forms of hereditary amyloidosis, this rare type displays amyloid deposition predominantly in the eyes and central …
Needle-shaped deposits on retinal surface in a case of ocular amyloidosis.
Hattori T, Shimada H, Yuzawa M, Kinukawa N, Fukuda T, Yasuda N. Hattori T, et al. Eur J Ophthalmol. 2008 May-Jun;18(3):473-5. doi: 10.1177/112067210801800329. Eur J Ophthalmol. 2008. PMID: 18465738
RESULTS: Glass wool-like opacities were observed during vitrectomy. Postoperative fundus examination of the right eye showed retinal hemorrhage and white deposits around blood vessels and on retinal surface. ...CONCLUSIONS: In this case, OCT showed needle-shaped …
RESULTS: Glass wool-like opacities were observed during vitrectomy. Postoperative fundus examination of the right eye showed retinal …
12 results