scholarly article | Q13442814 |
P2093 | author name string | McKechnie NM | |
MacDonald MK | |||
Duvall-Young J | |||
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Immune-Complex Deposition in the Eye in Systemic Lupus Erythematosus | Q39901385 | ||
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Toxemia of pregnancy. An angiographic interpretation of fundus changes | Q44273399 | ||
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Fundus lesions in malignant hypertension. I. A pathologic study of experimental hypertensive choroidopathy | Q49229070 | ||
Central Retinal Vein Occlusion Following Peritoneal Dialysis | Q54447352 | ||
Characterization of mixed membranous and proliferative glomerulonephritis: recognition of three varieties | Q69370717 | ||
The eye in malignant hypertension | Q69373353 | ||
Corneal crystalline deposits and drusenosis associated with IgA-kappa chain monoclonal gammopathy | Q69948574 | ||
Intraocular Pressure Changes During Hemodialysis | Q70600137 | ||
Choroidal vascular changes in toxemia of pregnancy | Q71175478 | ||
Ischemic infarcts of the choroid (Elschinig spots). A cause of retinal separation in hypertensive disease with renal insufficiency. A clinical and histopathologic study | Q72233669 | ||
Retinopathies of chronic glomerulonephritis. A study of cases treated with renal transplantation | Q72752278 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | glomerulonephritis | Q605006 |
drusen | Q1140528 | ||
P304 | page(s) | 297-302 | |
P577 | publication date | 1989-04-01 | |
P1433 | published in | British Journal of Ophthalmology | Q13443571 |
P1476 | title | Fundus changes in (type II) mesangiocapillary glomerulonephritis simulating drusen: a histopathological report | |
P478 | volume | 73 |
Q58739269 | A long history of dense deposit disease |
Q37327009 | A microstructural retinal analysis of membrano-proliferative glomerulonephritis type II. |
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Q37994185 | Alport syndrome, basement membranes and collagen |
Q27004686 | Animal models of age related macular degeneration |
Q46510049 | Benign Yellow Dot Maculopathy: A New Macular Phenotype. |
Q38616354 | Complement Activation and Inhibition in Retinal Diseases |
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Q34574482 | Current concepts in C3 glomerulopathy |
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Q37304040 | Electrophysiology of type II mesangiocapillary glomerulonephritis with associated fundus abnormalities |
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Q36804333 | Heparan sulfate, including that in Bruch's membrane, inhibits the complement alternative pathway: implications for age-related macular degeneration. |
Q35449598 | High-speed ultrahigh-resolution OCT of Bruch's membrane in membranoproliferative glomerulonephritis type 2. |
Q33953345 | Is renal function associated with early age-related macular degeneration? |
Q33260025 | Macular degeneration: recent advances and therapeutic opportunities. |
Q72542161 | Membranoproliferative glomerulonephritis type II associated with central serous retinopathy |
Q37510769 | Multimodal imaging of membranoproliferative glomerulonephritis type II. |
Q36860946 | New approaches to the treatment of dense deposit disease |
Q51169833 | Ocular complications after kidney transplantation: a case report and review of literature. |
Q38357009 | Oligosaccharide composition is similar in drusen and dense deposits in membranoproliferative glomerulonephritis type II. |
Q46491539 | Optical coherence tomography of fundus findings in type II mesangiocapillary glomerulonephritis |
Q26747262 | Overview of C3 Glomerulopathy |
Q37285079 | Oxidative stress renders retinal pigment epithelial cells susceptible to complement-mediated injury. |
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Q33845185 | Retinal basement membrane abnormalities and the retinopathy of Alport syndrome |
Q45064349 | Retinal changes associated with type 2 glomerulonephritis |
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Q46445669 | Retinal function abnormalities in membranoproliferative glomerulonephritis type II. |
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Q70153489 | Specific eye fundus lesions in type II membranoproliferative glomerulonephritis |
Q36464283 | Spontaneous Resolution of Retinal Pigment Epithelial Detachments and Visual Improvement in Patient with MPGN II: A Case Report |
Q43671971 | Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis. |
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Q30827994 | Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy). |
Q52704996 | The amplification loop of the complement pathways. |
Q34588115 | The significance of the complement system for the pathogenesis of age-related macular degeneration - current evidence and translation into clinical application |
Q35985754 | Vision-threatening retinal abnormalities in chronic kidney disease stages 3 to 5. |
Q28191783 | Visual impairment caused by retinal abnormalities in mesangiocapillary (membranoproliferative) glomerulonephritis type II ("dense deposit disease") |
Q64039956 | [Patient with type II membranoproliferative glomerulonephritis: intravitreal bevacizumab therapy for choroidal neovascularization] |
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