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2015 | 1 |
2017 | 1 |
2018 | 1 |
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Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome.
Clin J Am Soc Nephrol. 2015 Jun 5;10(6):1011-9. doi: 10.2215/CJN.08520814. Epub 2015 Apr 8.
Clin J Am Soc Nephrol. 2015.
PMID: 25854283
Free PMC article.
Reversal of threatening blindness after initiation of eculizumab in Purtscher-like retinopathy secondary to atypical hemolytic uremic syndrome.
Ramos de Carvalho JE, Schlingemann RO, Oranje M, Bemelman FJ, van Schooneveld MJ.
Ramos de Carvalho JE, et al.
Int Ophthalmol. 2018 Feb;38(1):399-407. doi: 10.1007/s10792-017-0470-1. Epub 2017 Mar 8.
Int Ophthalmol. 2018.
PMID: 28275964
Free PMC article.
We revisit the etiology of Purtscher-like retinopathy based on the rapid response and profound visual improvement after initiation of systemic intravenous eculizumab, an inhibitor of the complement cascade, in a patient with Purtscher-like retinopathy secondary to familial …
We revisit the etiology of Purtscher-like retinopathy based on the rapid response and profound visual improvement after initiation of system …
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