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Items: 1 to 20 of 47

1.
Corneal amyloidosis.
J Watts, H Frank
Br J Ophthalmol. 1989 Aug; 73(8): 674–676. doi: 10.1136/bjo.73.8.674
PMCID:
PMC1041844
SummaryPage BrowsePDF–848K
2.
Corneal amyloidosis caused by Leu518Pro mutation of βig-h3 gene
K. Hirano, Y. Hotta, K. Fujiki, A. Kanai
Br J Ophthalmol. 2000 Jun; 84(6): 583–585. doi: 10.1136/bjo.84.6.583
PMCID:
PMC1723504
SummaryPDF–185K
3.
Findings of secondary corneal amyloidosis with ultrahigh-resolution optical coherence tomography
Kaoru Araki-Sasaki, Yasuhiro Osakabe, Hideki Fukuoka, Ryuichi Ideta, Koji Hirano
Clin Ophthalmol. 2014; 8: 2115–2119. Published online 2014 Oct 14. doi: 10.2147/OPTH.S70759
PMCID:
PMC4206355
AbstractArticlePDF–1.9M
4.
Collagen fiber changes related to keratoconus with secondary corneal amyloidosis
Kaoru Araki-Sasaki, Yasuhiro Osakabe, Koji Fujita, Kazunori Miyata, Koji Hirano
Int Med Case Rep J. 2018; 11: 193–199. Published online 2018 Aug 30. doi: 10.2147/IMCRJ.S162655
PMCID:
PMC6121752
AbstractArticlePDF–6.7M
5.
Primary gelatinous drop-like keratopathy.
D S Gartry, M G Falcon, R W Cox
Br J Ophthalmol. 1989 Aug; 73(8): 661–664. doi: 10.1136/bjo.73.8.661
PMCID:
PMC1041841
SummaryPage BrowsePDF–1.1M
6.
Lactoferrin Glu561Asp facilitates secondary amyloidosis in the cornea
K Araki-Sasaki, Y Ando, M Nakamura, K Kitagawa, S Ikemizu, T Kawaji, T Yamashita, M Ueda, K Hirano, M Yamada, K Matsumoto, S Kinoshita, H Tanihara
Br J Ophthalmol. 2005 Jun; 89(6): 684–688. doi: 10.1136/bjo.2004.056804
PMCID:
PMC1772658
AbstractArticlePDF–209K
7.
A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy
Yang Jing, Chun Liu, Liya Wang
Mol Vis. 2009; 15: 1580–1588. Published online 2009 Aug 14.
PMCID:
PMC2728569
AbstractArticlePDF–11M
8.
Two novel mutations identified in two Chinese gelatinous drop-like corneal dystrophy families
Bei Zhang, Yu-Feng Yao, Ping Zhou
Mol Vis. 2007; 13: 988–992. Published online 2007 Jun 24.
PMCID:
PMC2774463
AbstractArticlePDF–176K
9.
Two novel mutations of TACSTD2 found in three Japanese gelatinous drop-like corneal dystrophy families with their aberrant subcellular localization
Mina Nakatsukasa, Satoshi Kawasaki, Kenta Yamasaki, Hideki Fukuoka, Akira Matsuda, Kohji Nishida, Shigeru Kinoshita
Mol Vis. 2011; 17: 965–970. Published online 2011 Apr 19.
PMCID:
PMC3084224
AbstractArticlePDF–5.7M
10.
Repeat deep anterior lamellar keratoplasty (DALK) for failed primary DALK
Ritu Arora, Abhilasha Sanoria, Parul Jain, Isha Gupta, Palak Gupta
Indian J Ophthalmol. 2023 Jun; 71(6): 2462–2465. Published online 2023 Jun 14. doi: 10.4103/IJO.IJO_2505_22
PMCID:
PMC10417964
AbstractArticlePDF–724K
11.
Immunohistochemical analysis of lattice corneal dystrophies types I and II.
T Kivelä, A Tarkkanen, I McLean, J Ghiso, B Frangione, M Haltia
Br J Ophthalmol. 1993 Dec; 77(12): 799–804. doi: 10.1136/bjo.77.12.799
PMCID:
PMC504660
SummaryPage BrowsePDF–2.7M
12.
Co-localisation of advanced glycation end products and d-β-aspartic acid-containing proteins in gelatinous drop-like corneal dystrophy
Yuichi Kaji, Tetsuro Oshika, Yutaka Takazawa, Masashi Fukayama, Noriko Fujii
Br J Ophthalmol. 2012 Aug; 96(8): 1127–1131. Published online 2012 Jun 13. doi: 10.1136/bjophthalmol-2012-301728
PMCID:
PMC3404710
AbstractArticlePDF–306K
13.
Nasal and ocular amyloidosis in a 15-year-old horse
Liv Østevik, Gjermund Gunnes, Gustavo A de Souza, Tale N Wien, Randi Sørby
Acta Vet Scand. 2014; 56(1): 50. Published online 2014 Aug 27. doi: 10.1186/s13028-014-0050-6
PMCID:
PMC4223893
AbstractArticlePDF–3.1M
14.
Graft rejection-like reactions in the early postoperative period after deep anterior lamellar keratoplasty for keratoconus: a retrospective study
Koji Hirano, Hidenori Tanaka, Kumiko Kato, Kaoru Araki-Sasaki
Clin Ophthalmol. 2018; 12: 2315–2322. Published online 2018 Nov 14. doi: 10.2147/OPTH.S178161
PMCID:
PMC6241761
AbstractArticlePDF–1.0M
15.
Deep Learning Algorithms for Corneal Amyloid Deposition Quantitation in Familial Amyloidosis
Klaus Kessel, Jaakko Mattila, Nina Linder, Tero Kivelä, Johan Lundin
Ocul Oncol Pathol. 2020 Jan; 6(1): 58–65. Published online 2019 Jul 15. doi: 10.1159/000500896
PMCID:
PMC6984152
AbstractArticlePDF–1.0M
16.
IC3D Classification of Corneal Dystrophies—Edition 3
Jayne S. Weiss, Christopher J. Rapuano, Berthold Seitz, Massimo Busin, Tero T. Kivelä, Nacim Bouheraoua, Cecilie Bredrup, Ken K. Nischal, Harshvardhan Chawla, Vincent Borderie, Kenneth R. Kenyon, Eung Kweon Kim, Hans Ulrik Møller, Francis L. Munier, Tim Berger, Walter Lisch
Cornea. 2024 Apr; 43(4): 466–527. Published online 2024 Feb 12. doi: 10.1097/ICO.0000000000003420
PMCID:
PMC10906208
AbstractArticlePDF–3.6M
17.
The serine protease HtrA1 cleaves misfolded transforming growth factor β–induced protein (TGFBIp) and induces amyloid formation
Ebbe Toftgaard Poulsen, Nadia Sukusu Nielsen, Carsten Scavenius, Emilie Hage Mogensen, Michael W. Risør, Kasper Runager, Marie V. Lukassen, Casper B. Rasmussen, Gunna Christiansen, Mette Richner, Henrik Vorum, Jan J. Enghild
J Biol Chem. 2019 Aug 2; 294(31): 11817–11828. Published online 2019 Jun 13. doi: 10.1074/jbc.RA119.009050
PMCID:
PMC6682723
AbstractArticlePDF–2.8M
18.
Confirmation of Association of TGFBI p.Ser591Phe Mutation with Variant Lattice Corneal Dystrophy
Charlene H. Choo, Doug D. Chung, Kaitlyn V. Ledwitch, Alexa Kassels, Jens Meiler, Anthony J. Aldave
Ophthalmic Genet. Author manuscript; available in PMC 2023 Aug 1.
Published in final edited form as: Ophthalmic Genet. 2022 Aug; 43(4): 530–533. Published online 2022 Mar 22. doi: 10.1080/13816810.2022.2050766
PMCID:
PMC9463079
AbstractArticlePDF–619K
19.
Ocular Involvement in Hereditary Amyloidosis
Angelo Maria Minnella, Roberta Rissotto, Elena Antoniazzi, Marco Di Girolamo, Marco Luigetti, Martina Maceroni, Daniela Bacherini, Benedetto Falsini, Stanislao Rizzo, Laura Obici
Genes (Basel) 2021 Jul; 12(7): 955. Published online 2021 Jun 22. doi: 10.3390/genes12070955
PMCID:
PMC8304974
AbstractArticlePDF–4.4M
20.
Ocular Involvement in Hereditary Transthyretin Amyloidosis: A Case Series Describing Novel Potential Biomarkers
Angelo Maria Minnella, Roberta Rissotto, Martina Maceroni, Angela Romano, Romina Fasciani, Marco Luigetti, Mario Sabatelli, Stanislao Rizzo, Benedetto Falsini
Genes (Basel) 2021 Jun; 12(6): 927. Published online 2021 Jun 18. doi: 10.3390/genes12060927
PMCID:
PMC8234990
AbstractArticlePDF–2.6M

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