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1  visual function in children and adults with Leber's congenital amaurosis.
2                   Mutations in RPGRIP1 cause Leber's congenital amaurosis.
3 e a severe recessive blinding disease called Leber's congenital amaurosis.
4    Thus, the rd chicken is a model for human Leber's congenital amaurosis.
5  with other retinal degenerations, including Leber's congenital amaurosis.
6 d dystrophies (CORD6) and recessive forms of Leber's congenital amaurosis.
7 s and patients with retinitis pigmentosa and Leber's congenital amaurosis.
8 mily of proteins that was recently linked to Leber's congenital amaurosis 3 (LCA).
9 eration in the rd3 mouse strain and in human Leber's congenital amaurosis, a congenital retinal dystr
10                     Mutations in RPE65 cause Leber's congenital amaurosis, a progressive retinal dege
11                     Retinal gene therapy for Leber's congenital amaurosis, an autosomal recessive chi
12 undus, which included congenital infections, Leber's Congenital Amaurosis and Aicardy syndrome.
13  An autosomal dominant retinitis pigmentosa, Leber's congenital amaurosis, autosomal dominant cone de
14 erlaps with regions attributed previously to Leber's congenital amaurosis, central areolar choroidal
15         In the Rpe65(-/-) mouse, a model for Leber's congenital amaurosis, cones degenerate much more
16 ents (aged 8-44 years) with RPE65-associated Leber's congenital amaurosis given one subretinal inject
17  Recent clinical trials for the treatment of Leber's congenital amaurosis have provided evidence for
18                                              Leber's congenital amaurosis (LCA) is a group of inherit
19                                              Leber's congenital amaurosis (LCA) is a known inherited
20                                              Leber's congenital amaurosis (LCA) is a rare blinding di
21 encing of DNA from 36 patients affected with Leber's congenital amaurosis (LCA), 62 with autosomal re
22  The most common form of blindness at birth, Leber's congenital amaurosis (LCA), is inherited in an a
23 derlying the non-syndromic blinding disorder Leber's congenital amaurosis (LCA).
24 the most frequently observed IRD followed by Leber's congenital amaurosis (LCA).
25 ed with multiple blinding diseases including Leber's Congenital Amaurosis (LCA).
26 e to debilitating ocular diseases, including Leber's congenital amaurosis (LCA).
27 stationary night blindness (CSNB), recessive Leber's congenital amaurosis (LCA1), and dominant cone-r
28 ular degeneration, retinitis pigmentosa, and Leber's congenital amaurosis matched well with data from
29 s in reversing blindness in animal models of Leber's congenital amaurosis, several groups proceeded w
30                                            A Leber's congenital amaurosis, termed LCA1, involves F514
31 , X-linked Severe Combined Immunodeficiency, Leber's Congenital Amaurosis Type 2 and in cancer immuno
32 ic interval and previously was implicated in Leber's congenital amaurosis, was screened for mutations
33 e-rod dystrophy-2, retinitis pigmentosa, and Leber's congenital amaurosis, which lead to loss of visi
34 tential treatments for retinitis pigmentosa, Leber's congenital amaurosis, X-linked retinoschisis, Be