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1 ment epithelium that manifests clinically as pigmentary retinopathy.
2 nces, bull's eye maculopathy, and peripheral pigmentary retinopathy.
3 white flashes in 15 patients with unilateral pigmentary retinopathy.
4 phthalmoparesis, mitochondrial myopathy, and pigmentary retinopathy also had autoimmune polyglandular
7 essive diseases characterized by progressive pigmentary retinopathy and sensorineural hearing loss.
8 alcium deposits, cutaneous photosensitivity, pigmentary retinopathy and/or cataracts, and sensorineur
9 abnormalities, such as cleft lip and palate, pigmentary retinopathy, and multiple tubular stenoses (e
10 tic neuropathy, ophthalmoplegia with ptosis, pigmentary retinopathy, and retrochiasmal visual loss.
11 alcium deposits; cutaneous photosensitivity; pigmentary retinopathy, cataracts, or both; and sensorin
12 (SD-OCT) findings of a patient who developed pigmentary retinopathy following high-dose deferoxamine
13 syndrome, Goldman-Favre syndrome and clumped pigmentary retinopathy in humans, allelic disorders caus
14 and serous retinal detachments, a unilateral pigmentary retinopathy mimicking retinitis pigmentosa, n
15 cessive Bardet-Biedl syndrome (BBS; obesity, pigmentary retinopathy, polydactyly, hypogonadism, renal
16 ome (BBS) which is characterized by obesity, pigmentary retinopathy, polydactyly, renal abnormalities
17 sorder with the primary features of obesity, pigmentary retinopathy, polydactyly, renal malformations
18 sorder with the primary features of obesity, pigmentary retinopathy, polydactyly, renal malformations
19 recessive disorder characterized by obesity, pigmentary retinopathy, polydactyly, renal malformations
20 ted neurodegeneration (PKAN), which leads to pigmentary retinopathy, progressive dystonia and other a
23 yndrome, Goldman-Favre syndrome, and clumped pigmentary retinopathy that is also associated with an a
25 report a case of bilateral nanophthalmos and pigmentary retinopathy with angle closure glaucoma and o