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1 as devoid of MG rip apart, a defect known as retinoschisis.
2 nal thickness decreases with age in X-linked retinoschisis.
3 n impairment in young males, called X-linked retinoschisis.
4 etinal hole, and typical degenerative senile retinoschisis.
5 come from a recent investigation in X-linked retinoschisis, a currently untreatable retinopathy.
6 s mutated, as it occurs in X-linked juvenile retinoschisis, a disease that results in morphological a
7 nked retinoschisis gene (RS1) cause X-linked retinoschisis, a form of progressive blindness.
8 riteria included a family history of macular retinoschisis, a known genetic abnormality associated wi
9              Most cases of X-linked juvenile retinoschisis and degenerative retinoschisis never requi
10 eted protein implicated in X-linked juvenile retinoschisis and essential for the structural and funct
11 uch as macular Berlin's edema, midperipheral retinoschisis, and choroidal and retinal detachment migh
12  choroidal melanoma; and intraretinal edema, retinoschisis, and retinal thinning overlying irradiated
13 tosa, Leber's congenital amaurosis, X-linked retinoschisis, Best's disease, Stargardt's disease, and
14 e discovery that retinal folds and traumatic retinoschisis can very rarely occur after crush head inj
15 ERG waveform that is characteristic of human retinoschisis disease and that implicates a synaptic tra
16        This new locus (RP23) encompasses the retinoschisis disease gene; therefore, XLRS1 was screene
17 he coding region of the gene responsible for retinoschisis do not cause RP23.
18 , loss-of-function mutations in the X-linked retinoschisis gene (RS1) cause X-linked retinoschisis, a
19  was amplified with primers specific for the retinoschisis gene (XLRS1), and the products were screen
20 holog (Xlrs1) of the human X-linked juvenile retinoschisis gene (XLRS1).
21 nine hydroxylase, paired box 6, the X-linked retinoschisis gene and TSC2/tuberin.
22 ulitis, whereas congenital disorders such as retinoschisis had the worst.
23  therapy will benefit patients with X-linked retinoschisis in a forthcoming clinical trial.
24 -photoreceptor phenotype similar to X-linked retinoschisis in young males.
25 ings feature residues implicated in X-linked retinoschisis, indicating the importance of correct asse
26                               Thus, X-linked retinoschisis is caused by abnormalities in a putative s
27                                     X-linked retinoschisis is characterized by microcystic-like chang
28 treomacular traction syndrome, macular hole, retinoschisis, macular edema, central serous chorioretin
29                                  An X-linked retinoschisis mouse (Rs1h-KO) model was created by subst
30  a known genetic abnormality associated with retinoschisis, myopic traction maculopathy, epiretinal m
31 nked juvenile retinoschisis and degenerative retinoschisis never require any type of surgical interve
32 ore, our data suggest that X-linked juvenile retinoschisis originates from abnormalities in a photore
33 ss and volume measurements were increased in retinoschisis patients compared to controls.
34 ss and volume measurements were decreased in retinoschisis patients compared to controls.
35 s and volumes were consistently increased in retinoschisis patients relative to controls.
36                          The mean age of the retinoschisis patients was 26.4 years.
37        Foveal schisis was observed in 81% of retinoschisis patients.
38 inal detachment, typical degenerative senile retinoschisis, peripheral laser coagulation scars, ora t
39 actors can contribute to the severity of the retinoschisis phenotype.
40                                     X-linked retinoschisis results in visual loss in early life with
41 5 years of age underwent genotyping, and the retinoschisis (RS1) mutations were classified as less se
42                                    A macular retinoschisis was detected in 5 eyes (31%), decreased el
43 three eyes of 33 male patients with X-linked retinoschisis were gleaned from a SD OCT database at the
44 ructural features of human X-linked juvenile retinoschisis with dissection through, and disorganizati
45 ble option in the treatment of patients with retinoschisis without causing significant cellular damag
46  family (a total of 18 members)with X-linked retinoschisis (XLRS) and detected a novel mutations of c
47 istent with human clinical X-linked juvenile retinoschisis (XLRS) in showing schisis cavities, which
48                                     X-linked retinoschisis (XLRS) is a form of macular degeneration w
49                                     X-linked retinoschisis (XLRS) is an inherited form of macular deg
50  The human retinal synaptic disease X-linked retinoschisis (XLRS) is characterized by impaired visual
51                                     X-linked Retinoschisis (XLRS) is one of the most common macular d
52 e cone system typically observed in X-linked retinoschisis (XLRS) represents a relatively greater def
53                    Individuals with X-linked retinoschisis (XLRS) show a comparatively greater reduct
54 oschisin gene, RS-1, cause juvenile X-linked retinoschisis (XLRS), a dystrophy characterized by delam
55 at encode retinoschisin (RS1) cause X-linked retinoschisis (XLRS), a form of juvenile macular and ret
56 ions in the RS1 gene cause X-linked juvenile retinoschisis (XLRS), a hereditary retinal dystrophy.
57                            X-linked juvenile retinoschisis (XLRS), a leading cause of juvenile macula
58 architecture with mutations causing X-linked retinoschisis (XLRS), a monogenic form of macular degene
59 tations in the NR2E3 gene, juvenile X-linked retinoschisis (XLRS), and some other retinal dystrophies

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