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Retained visual function in a subset of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD).
Ophthalmic Genet. 2021 Feb;42(1):23-27. doi: 10.1080/13816810.2020.1836658. Epub 2020 Oct 27.
Ophthalmic Genet. 2021.
PMID: 33107778
Introduction: LCHADD causes retinopathy associated with low vision, visual field defects, nyctalopia and myopia. We report a retrospective long-term single-center study of 6 LCHADD patients trying to clarify if early diagnosis has an impact on the course and outcome of cho …
Introduction: LCHADD causes retinopathy associated with low vision, visual field defects, nyctalopia and myopia. We report a retrospective l …
Oxalate retinopathy is irreversible despite early combined liver-kidney transplantation in primary hyperoxaluria type 1.
Atiskova Y, Dulz S, Schmäschke K, Oh J, Grabhorn E, Kemper MJ, Brinkert F.
Atiskova Y, et al. Among authors: dulz s.
Am J Transplant. 2019 Dec;19(12):3328-3334. doi: 10.1111/ajt.15484. Epub 2019 Jun 27.
Am J Transplant. 2019.
PMID: 31152479
Free article.
After CLKT, systemic oxalosis decreases continuously, although only insufficient data are available regarding oxalate retinopathy (ROx), leading to severe visual impairment. We analyzed long-term follow-up data of ROx in 13 patients undergoing CLKT for PH1 at our center be …
After CLKT, systemic oxalosis decreases continuously, although only insufficient data are available regarding oxalate retinopathy (ROx), lea …
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