ライフサイエンスコーパス: Leber's congenital amaurosis

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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 Mutations in RPE65 cause Leber's congenital amaurosis, a progressive retinal dege

10 Retinal gene therapy for Leber's congenital amaurosis, an autosomal recessive chi

11 An autosomal dominant retinitis pigmentosa, Leber's congenital amaurosis, autosomal dominant cone de

12 erlaps with regions attributed previously to Leber's congenital amaurosis, central areolar choroidal

13 In the Rpe65(-/-) mouse, a model for Leber's congenital amaurosis, cones degenerate much more

14 ents (aged 8-44 years) with RPE65-associated Leber's congenital amaurosis given one subretinal inject

15 Recent clinical trials for the treatment of Leber's congenital amaurosis have provided evidence for

16 Leber's congenital amaurosis (LCA) is a group of inherit

17 encing of DNA from 36 patients affected with Leber's congenital amaurosis (LCA), 62 with autosomal re

18 The most common form of blindness at birth, Leber's congenital amaurosis (LCA), is inherited in an a

19 ed with multiple blinding diseases including Leber's Congenital Amaurosis (LCA).

20 e to debilitating ocular diseases, including Leber's congenital amaurosis (LCA).

21 derlying the non-syndromic blinding disorder Leber's congenital amaurosis (LCA).

22 ular degeneration, retinitis pigmentosa, and Leber's congenital amaurosis matched well with data from

23 s in reversing blindness in animal models of Leber's congenital amaurosis, several groups proceeded w

24 A Leber's congenital amaurosis, termed LCA1, involves F514

25 , X-linked Severe Combined Immunodeficiency, Leber's Congenital Amaurosis Type 2 and in cancer immuno

26 ic interval and previously was implicated in Leber's congenital amaurosis, was screened for mutations

27 e-rod dystrophy-2, retinitis pigmentosa, and Leber's congenital amaurosis, which lead to loss of visi

28 tential treatments for retinitis pigmentosa, Leber's congenital amaurosis, X-linked retinoschisis, Be

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