首页 > 按专业查询名词 > 查询PubMed相关文献
名词信息
Pubmed相关的文献
vitreoretinal degeneration (Wagner disease)相关文献:
Wagner vitreoretinal degeneration. Follow-up of the original pedigree.
Graemiger RA, Niemeyer G, Schneeberger SA, Messmer EP.
Ophthalmology. 1995 Dec;102(12):1830-9. doi: 10.1016/s0161-6420(95)30787-7.
PMID:9098284
Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14.
Zech JC, Morlé L, Vincent P, Alloisio N, Bozon M, Gonnet C, Milazzo S, Grange JD, Trepsat C, Godet J, Plauchu H.
Graefes Arch Clin Exp Ophthalmol. 1999 May;237(5):387-93. doi: 10.1007/s004170050249.
PMID:10333105
Snowflake vitreoretinal degeneration: follow-up of the original family.
Lee MM, Ritter R 3rd, Hirose T, Vu CD, Edwards AO.
Ophthalmology. 2003 Dec;110(12):2418-26. doi: 10.1016/S0161-6420(03)00828-5.
PMID:14644728
Multimodal Retinal Imaging Findings in Two Cousins With VCAN-Related Vitreoretinopathy or Wagner Disease.
Parra MM, Spoth E, Ronquillo CC, Henderson R, Hartnett ME.
Ophthalmic Surg Lasers Imaging Retina. 2022 Nov;53(11):639-643. doi: 10.3928/23258160-20221026-01. Epub 2022 Nov 1.
PMID:36378611
Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36.
Jiao X, Ritter R 3rd, Hejtmancik JF, Edwards AO.
Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4498-503. doi: 10.1167/iovs.04-0722.
PMID:15557460
Spectral-Domain Optical Coherence Tomography in Wagner Syndrome: Characterization of Vitreoretinal Interface and Foveal Changes.
Rothschild PR, Burin-des-Roziers C, Audo I, Nedelec B, Valleix S, Brézin AP.
Am J Ophthalmol. 2015 Nov;160(5):1065-1072.e1. doi: 10.1016/j.ajo.2015.08.012. Epub 2015 Aug 15.
PMID:26284746
VCAN Canonical Splice Site Mutation is Associated With Vitreoretinal Degeneration and Disrupts an MMP Proteolytic Site.
Tang PH, Velez G, Tsang SH, Bassuk AG, Mahajan VB.
Invest Ophthalmol Vis Sci. 2019 Jan 2;60(1):282-293. doi: 10.1167/iovs.18-25624.
PMID:30657523
Posterior chorioretinal atrophy and vitreous phenotype in a family with Stickler syndrome from a mutation in the COL2A1 gene.
Vu CD, Brown J Jr, Körkkö J, Ritter R 3rd, Edwards AO.
Ophthalmology. 2003 Jan;110(1):70-7. doi: 10.1016/s0161-6420(02)01446-x.
PMID:12511349
WAGNER syndrome: anatomic, functional and genetic characterization of a Portuguese family.
Araújo JR, Tavares-Ferreira J, Estrela-Silva S, Rocha P, Brandão E, Faria PA, Falcão-Reis F, Rocha-Sousa A.
Graefes Arch Clin Exp Ophthalmol. 2018 Jan;256(1):163-171. doi: 10.1007/s00417-017-3800-0. Epub 2017 Oct 25.
PMID:29071374
WIDEFIELD SWEPT-SOURCE OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY FINDINGS IN WAGNER SYNDROME.
Bleicher ID, Garg I, Hoyek S, Place E, Miller JB, Patel NA.
Retin Cases Brief Rep. 2024 Jan 1;18(1):80-86. doi: 10.1097/ICB.0000000000001307.
PMID:36007184
© Copyright 2021 鸿泰茂源  版权所有All Rights Reserved京ICP备11040441号-3