コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 in two unrelated Lowe syndrome patients with congenital glaucoma.
2 s the initial surgical procedure for primary congenital glaucoma.
3 cup-to-disc (C/D) ratio greater in secondary congenital glaucoma.
4 ve changes, occlusion of the visual axis, or congenital glaucoma.
8 ts (60 eyes) analyzed with bilateral primary congenital glaucoma aged </=2 years, 1 eye of each patie
9 atients with unilateral or bilateral primary congenital glaucoma aged less than 2 years were randomiz
10 f the 6p25 breakpoint in a patient with both congenital glaucoma and a balanced-translocation event i
11 l length was significantly longer in primary congenital glaucoma and cup-to-disc (C/D) ratio greater
12 Although most glaucoma patients are elderly, congenital glaucoma and glaucomas of childhood are also
14 in humans with genetic eye diseases such as congenital glaucoma and microspherophakia, indicating a
15 hy with a predilection for the macular area, congenital glaucoma and optical nerve hypoplasia, and op
16 try provides unique baseline data on primary congenital glaucoma and secondary congenital glaucoma in
18 venile GLC1A glaucoma, a P450 gene for GLC3A congenital glaucoma, and a bicoidhomeobox transcription
19 p25 region is now implicated in FGI, primary congenital glaucoma, and iridogoniodysgenesis anomaly.
20 tter for specific diagnoses, such as primary congenital glaucoma, aphakic glaucoma, and glaucomas ass
21 syndrome, a rare condition characterized by congenital glaucoma, as well as craniofacial, skeletal,
33 on primary congenital glaucoma and secondary congenital glaucoma in Saudi Arabia that will enable us
35 and GLC3B) have been identified for primary congenital glaucoma, one locus (GLC1A) for juvenile-onse
36 atio and corneal haze, whereas for secondary congenital glaucoma only axial length was positively cor
37 The medical records of patients with primary congenital glaucoma over a 23-year period were reviewed:
39 2, and MYOC mutations in a cohort of primary congenital glaucoma patients from the United States, app
40 st primary congenital glaucoma and secondary congenital glaucoma patients had bilateral disease (82.6
41 uencing, may identify novel genes in primary congenital glaucoma patients who have no mutations in kn
42 The annual incidence of diagnosis of primary congenital glaucoma (PCG) in Great Britain was 5.41 in 1
48 The autosomal recessive disorder primary congenital glaucoma (PCG) is caused by unknown developme
50 gene (CYP1B1) in five families with primary congenital glaucoma (PCG) linked to the GLC3A locus on c
52 uvenile open-angle glaucoma (OAG) or primary congenital glaucoma (PCG) with sustained postoperative i
53 ubject groups: two Siamese cats with primary congenital glaucoma (PCG), a control Siamese cat without
54 t of conventional angle surgeries in primary congenital glaucoma (PCG), as judged by glaucoma and vis
58 71 unaffected family members of the primary congenital glaucoma probands, and 101 healthy unrelated
60 angle surgeries show good success in primary congenital glaucoma, reported success in glaucoma follow
61 rrelation of OCRL1 mutations associated with congenital glaucoma revealed clustering of missense and
62 egistry data that included new patients with congenital glaucoma seen between 2001 and 2003 (29 month
63 coincide with a mutation of Tie2 in primary congenital glaucoma that leads to defective Tie2 cluster
64 f a new locus (designated GLC3B) for primary congenital glaucoma to the short arm of chromosome 1 (1p
65 was equally distributed by sex but secondary congenital glaucoma was 1.5-fold more common in male pat
66 ean (+/- SD) age at presentation for primary congenital glaucoma was 3.8 +/- 10.7 months and for seco
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。