Optical coherence tomography angiography analysis of fabry disease
暂无分享,去创建一个
[1] R. Manna,et al. Macular Impairment in Fabry Disease: A Morpho-functional Assessment by Swept-Source OCT Angiography and Focal Electroretinography. , 2019, Investigative ophthalmology & visual science.
[2] E. Riccio,et al. Optical Coherence Tomography Angiography Findings in Fabry Disease , 2019, Journal of clinical medicine.
[3] L. Michaud. Longitudinal study on ocular manifestations in a cohort of patients with Fabry disease , 2019, bioRxiv.
[4] Ali Erginay,et al. VESSEL DENSITY OF SUPERFICIAL, INTERMEDIATE, AND DEEP CAPILLARY PLEXUSES USING OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY , 2018, Retina.
[5] R. Malik,et al. Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease , 2018, Scientific Reports.
[6] D. Robertson,et al. Wide-Field In Vivo Confocal Microscopy of Meibomian Gland Acini and Rete Ridges in the Eyelid Margin , 2018, Investigative ophthalmology & visual science.
[7] G. Virgili,et al. Optical Coherence Tomography Angiography in Fabry disease , 2018 .
[8] C. Framme,et al. Density of the Retinal Blood Flow and Thickness Mapping by Spectralis OCT in Patients with Fabry Disease , 2018 .
[9] Mayss Al-Sheikh,et al. Optical Coherence Tomography Angiography findings in patients with Fabry's disease , 2018 .
[10] M. Ersoz,et al. Cilioretinal artery occlusion and anterior ischemic optic neuropathy as the initial presentation in a child female carrier of Fabry disease , 2018, International Ophthalmology.
[11] A. Mecocci,et al. COMPUTER ASSISTED RETINAL VESSEL TORTUOSITY EVALUATION IN NOVEL MUTATION FABRY DISEASE: Towards New Prognostic Markers , 2017, Retina.
[12] Erika Phillips,et al. Visualization of Radial Peripapillary Capillaries Using Optical Coherence Tomography Angiography: The Effect of Image Averaging , 2017, PloS one.
[13] N. Karabul,et al. Ocular Signs Correlate Well with Disease Severity and Genotype in Fabry Disease , 2015, PLoS ONE.
[14] Melanie D Sivley. Fabry Disease: A Review of Ophthalmic and Systemic Manifestations , 2013, Optometry and vision science : official publication of the American Academy of Optometry.
[15] D. Germain. Fabry disease , 2010, Orphanet journal of rare diseases.
[16] M. Browning,et al. Ocular manifestations of Fabry disease within in a single kindred. , 2010, Optometry.
[17] R. Schiffmann,et al. Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data , 2009, The Lancet.
[18] S. Pitz,et al. Subclinical optic neuropathy in Fabry disease , 2009, Ophthalmic genetics.
[19] Y. Iino,et al. Thrombosis in Japanese patients with Fabry disease , 2009, Journal of the Neurological Sciences.
[20] N. Samiy. Ocular features of Fabry disease: diagnosis of a treatable life-threatening disorder. , 2008, Survey of ophthalmology.
[21] U. Ramaswami,et al. Enzyme replacement therapy with agalsidase alfa in children with Fabry disease , 2007, Acta paediatrica.
[22] A. Mehta,et al. Ocular manifestations of Fabry’s disease: data from the Fabry Outcome Survey , 2006, British Journal of Ophthalmology.
[23] R. Desnick,et al. High incidence of later-onset fabry disease revealed by newborn screening. , 2006, American journal of human genetics.
[24] Alki Liasis,et al. Visual electrophysiology in patients with Anderson-Fabry disease , 2006 .
[25] K. Nicholls,et al. Ophthalmological manifestations of Fabry disease: a survey of patients at the Royal Melbourne Fabry Disease Treatment Centre , 2005, Clinical & experimental ophthalmology.
[26] M. Brys,et al. Reduced cerebral blood flow velocity and impaired cerebral autoregulation in patients with Fabry disease , 2004, Journal of Neurology.
[27] C. Orssaud,et al. Ocular manifestations in Fabry disease: a survey of 32 hemizygous male patients , 2003, Ophthalmic genetics.
[28] G. Pastores,et al. Anderson-Fabry Disease: Extrarenal, Neurologic Manifestations , 2002 .
[29] R. A. Wevers,et al. The frequency of lysosomal storage diseases in The Netherlands , 1999, Human Genetics.
[30] E. Uyama,et al. High incidence of thrombosis in Fabry's disease. , 1997, Internal medicine.
[31] S. Tsuji. [Alpha-galactosidase A deficiency--Fabry's disease]. , 1988, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.
[32] R. Desnick,et al. The ocular manifestations in Fabry's disease. , 1979, Archives of ophthalmology.
[33] R. Desnick,et al. Central retinal artery occlusion complicating Fabry's disease. , 1978, Archives of ophthalmology.
[34] Yali Jia,et al. Optical Coherence Tomography Angiography Using the Optovue Device. , 2016, Developments in ophthalmology.
[35] P. Luna,et al. [Fabry disease]. , 2009, Anais brasileiros de dermatologia.
[36] D. Germain. Maladie de Fabry (déficit en α-galactosidase A): innovations thérapeutiques récentes , 2002 .
[37] M. Takagi,et al. Ischemic optic neuropathy in a female carrier with Fabry's disease. , 1992, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.
[38] D. Toussaint,et al. Tortuosities of retinal and conjunctival vessels in lysosomal storage diseases. , 1982, Birth defects original article series.
[39] Franceschetti At. Fabry disease: ocular manifestations. , 1976 .