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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.
6 s mutated, as it occurs in X-linked juvenile retinoschisis, a disease that results in morphological a
8 riteria included a family history of macular retinoschisis, a known genetic abnormality associated wi
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
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
25 ings feature residues implicated in X-linked retinoschisis, indicating the importance of correct asse
28 treomacular traction syndrome, macular hole, retinoschisis, macular edema, central serous chorioretin
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
38 inal detachment, typical degenerative senile retinoschisis, peripheral laser coagulation scars, ora t
41 5 years of age underwent genotyping, and the retinoschisis (RS1) mutations were classified as less se
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
50 The human retinal synaptic disease X-linked retinoschisis (XLRS) is characterized by impaired visual
52 e cone system typically observed in X-linked retinoschisis (XLRS) represents a relatively greater def
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.
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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