scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1035245947 |
P356 | DOI | 10.1038/KI.2008.658 |
P698 | PubMed publication ID | 19177159 |
P5875 | ResearchGate publication ID | 23957344 |
P50 | author | Carolyn J Jones | Q64358807 |
P2093 | author name string | Richard E Bonshek | |
Ian S D Roberts | |||
Colin D Short | |||
Yvonne B D'souza | |||
P2860 | cites work | A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration | Q24523983 |
Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease) | Q24655016 | ||
An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and age-related macular degeneration | Q28190470 | ||
Local cellular sources of apolipoprotein E in the human retina and retinal pigmented epithelium: implications for the process of drusen formation | Q30671842 | ||
Complement and diseases: defective alternative pathway control results in kidney and eye diseases | Q33367362 | ||
Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature | Q34293159 | ||
Complement activation and inflammatory processes in Drusen formation and age related macular degeneration | Q34521109 | ||
Membranoproliferative glomerulonephritis type II (dense deposit disease): an update | Q36084453 | ||
New approaches to the treatment of dense deposit disease | Q36860946 | ||
Fundus changes in (type II) mesangiocapillary glomerulonephritis simulating drusen: a histopathological report | Q42618487 | ||
Retinal changes associated with type 2 glomerulonephritis | Q45064349 | ||
Fundus changes in membranoproliferative glomerulonephritis type II. A fluorescein angiographic study of 23 patients | Q68038284 | ||
Glycoproteins of drusen and drusen-like lesions | Q81230321 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | oligosaccharide | Q320607 |
glomerulonephritis | Q605006 | ||
drusen | Q1140528 | ||
membranoproliferative glomerulonephritis | Q2299379 | ||
P304 | page(s) | 824-827 | |
P577 | publication date | 2009-01-28 | |
P1433 | published in | Kidney International | Q6404823 |
P1476 | title | Oligosaccharide composition is similar in drusen and dense deposits in membranoproliferative glomerulonephritis type II | |
P478 | volume | 75 |
Q35750545 | Age-Related Macular Degeneration: A Disease of Systemic or Local Complement Dysregulation? |
Q35580577 | Clinical features and outcomes of 98 children and adults with dense deposit disease. |
Q34130746 | Glycoprotein hyposialylation gives rise to a nephrotic-like syndrome that is prevented by sialic acid administration in GNE V572L point-mutant mice |
Q35449598 | High-speed ultrahigh-resolution OCT of Bruch's membrane in membranoproliferative glomerulonephritis type 2. |
Q37510769 | Multimodal imaging of membranoproliferative glomerulonephritis type II. |
Q47103639 | Multimodal imaging of retinal pigment epithelial detachments in patients with C3 glomerulopathy: case report and review of the literature |
Q53070119 | Primary Glomerulonephritis with Unique C4d Deposition and Concurrent Non-infectious Intermediate Uveitis: a Case Report and Literature Review. |
Q55710477 | Retinal Basal Laminar Deposits in Complement fH/fP Mouse Model of Dense Deposit Disease. |
Q38749961 | Retinal disease in the C3 glomerulopathies and the risk of impaired vision. |
Q47142300 | Retinal findings in membranoproliferative glomerulonephritis. |
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