MCID: XLN247
MIFTS: 21

X-Linked Congenital Retinoschisis

Categories: Eye diseases, Fetal diseases, Genetic diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for X-Linked Congenital Retinoschisis

MalaCards integrated aliases for X-Linked Congenital Retinoschisis:

Name: X-Linked Congenital Retinoschisis 25
X-Linked Retinoschisis 25

Classifications:



Summaries for X-Linked Congenital Retinoschisis

MalaCards based summary : X-Linked Congenital Retinoschisis, also known as x-linked retinoschisis, is related to retinoschisis 1, x-linked, juvenile and juvenile retinoschisis. An important gene associated with X-Linked Congenital Retinoschisis is RS1 (Retinoschisin 1). The drugs Brinzolamide and Dorzolamide have been mentioned in the context of this disorder. Affiliated tissues include retina, eye and pineal.

GeneReviews: NBK1222

Related Diseases for X-Linked Congenital Retinoschisis

Diseases in the Retinoschisis 1, X-Linked, Juvenile family:

X-Linked Congenital Retinoschisis

Diseases related to X-Linked Congenital Retinoschisis via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 74, show less)
# Related Disease Score Top Affiliating Genes
1 retinoschisis 1, x-linked, juvenile 30.4 RS1 CDKL5
2 juvenile retinoschisis 30.2 RS1 CDKL5
3 fundus dystrophy 29.3 RS1 CDKL5
4 retinal disease 10.5
5 macular holes 10.5
6 vitreoretinal dystrophy 10.4
7 macular retinal edema 10.4
8 retinal degeneration 10.4
9 strabismus 10.3
10 mechanical strabismus 10.3
11 retinal detachment 10.3
12 retinitis pigmentosa 10.2
13 yemenite deaf-blind hypopigmentation syndrome 10.2
14 microvascular complications of diabetes 5 10.2
15 complete androgen insensitivity syndrome 10.2
16 neuroretinitis 10.2
17 retinitis 10.2
18 vitreous detachment 10.2
19 inherited retinal disorder 10.2
20 retinoblastoma 10.2
21 retinoschisis of fovea 10.2
22 coats disease 10.2
23 intraocular pressure quantitative trait locus 10.2
24 neovascular glaucoma 10.2
25 eye disease 10.2
26 cataract 10.2
27 scotoma 10.2
28 pathologic nystagmus 10.2
29 pik3ca-related overgrowth syndrome 10.2
30 vitreoretinopathy, neovascular inflammatory 10.1
31 macular degeneration, age-related, 1 10.1
32 suppression amblyopia 10.1
33 amblyopia 10.1
34 bullous retinoschisis 10.1
35 refractive error 10.1
36 farsightedness 10.1
37 vitreoretinopathy 10.1
38 congenital heart defects, hamartomas of tongue, and polysyndactyly 10.0
39 persistent hyperplastic primary vitreous, autosomal recessive 10.0
40 proteasome-associated autoinflammatory syndrome 1 10.0
41 aging 10.0
42 cataract, age-related nuclear 10.0
43 astigmatism 10.0
44 night blindness, congenital stationary, type 1e 10.0
45 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.0
46 congenital stationary night blindness 10.0
47 cone dystrophy 10.0
48 persistent hyperplastic primary vitreous 10.0
49 stickler syndrome 10.0
50 sensorineural hearing loss 10.0
51 monocular esotropia 10.0
52 hypopyon 10.0
53 leukocoria 10.0
54 myopia 10.0
55 retinal ischemia 10.0
56 uveitis 10.0
57 color blindness 10.0
58 mature cataract 10.0
59 rubeosis iridis 10.0
60 ectropion 10.0
61 retinal vascular disease 10.0
62 bilateral retinoblastoma 10.0
63 situs inversus 10.0
64 night blindness 10.0
65 senile cataract 10.0
66 esotropia 10.0
67 oguchi disease 10.0
68 vitreoretinal degeneration 10.0
69 posttransplant acute limbic encephalitis 10.0
70 combined hamartoma of the retina and retinal pigment epithelium 10.0
71 nicolaides-baraitser syndrome 9.7 RS1 CDKL5
72 angelman syndrome 9.7 RS1 CDKL5
73 west syndrome 9.6 RS1 CDKL5
74 early infantile epileptic encephalopathy 9.6 RS1 CDKL5

Graphical network of the top 20 diseases related to X-Linked Congenital Retinoschisis:



Diseases related to X-Linked Congenital Retinoschisis

Symptoms & Phenotypes for X-Linked Congenital Retinoschisis

Drugs & Therapeutics for X-Linked Congenital Retinoschisis

Drugs for X-Linked Congenital Retinoschisis (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

(showing 4, show less)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1
Brinzolamide Approved 138890-62-7 68844
2
Dorzolamide Approved 120279-96-1 3154 5284549
3 Antihypertensive Agents
4 Carbonic Anhydrase Inhibitors

Interventional clinical trials:

(showing 4, show less)
# Name Status NCT ID Phase Drugs
1 A Phase I/IIa Study of RS1 Ocular Gene Transfer for X-linked Retinoschisis Recruiting NCT02317887 Phase 1, Phase 2
2 A Multiple-Site, Phase 1/2, Safety and Efficacy Trial of a Recombinant Adeno-associated Virus Vector Expressing Retinoschisin (rAAV2tYF-CB-hRS1) in Patients With X-linked Retinoschisis Active, not recruiting NCT02416622 Phase 1, Phase 2
3 Clinical Evaluation of Patients With X-linked Retinoschisis (XLRS) Completed NCT02331173 Dorzolamide 2% TID or brinzolamide 1% TID
4 Mothers' Experiences With X-linked Retinoschisis Compared to Fathers' Experiences Completed NCT03354403

Search NIH Clinical Center for X-Linked Congenital Retinoschisis

Genetic Tests for X-Linked Congenital Retinoschisis

Anatomical Context for X-Linked Congenital Retinoschisis

MalaCards organs/tissues related to X-Linked Congenital Retinoschisis:

40
Retina, Eye, Pineal

Publications for X-Linked Congenital Retinoschisis

Articles related to X-Linked Congenital Retinoschisis:

(showing 374, show less)
# Title Authors PMID Year
1
"There Are Hills and Valleys": Experiences of Parenting a Son With X-Linked Retinoschisis. 61 25
31765628 2020
2
Motivations and Decision Making Processes of Men With X-linked Retinoschisis Considering Participation in an Ocular Gene Therapy Trial. 25 61
30885710 2019
3
Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis. 61 25
30652005 2019
4
Multimodal imaging in a pedigree of X-linked Retinoschisis with a novel RS1 variant. 25 61
30419843 2018
5
Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis. 61 25
29739629 2018
6
Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery. 25 61
30196853 2018
7
X-linked juvenile retinoschisis: phenotypic and genetic characterization. 25 61
30450322 2018
8
Convergence of Human Genetics and Animal Studies: Gene Therapy for X-Linked Retinoschisis. 25 61
26101206 2015
9
Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypes. 25 61
23847049 2013
10
X-linked retinoschisis: RS1 mutation severity and age affect the ERG phenotype in a cohort of 68 affected male subjects. 61 25
22039241 2011
11
Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis. 25 61
20061330 2010
12
Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study. 25 61
19474399 2009
13
Molecular genetic characteristics of X-linked retinoschisis in Koreans. 25 61
19390641 2009
14
ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT. 61 25
17987333 2008
15
Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease. 25 61
16272055 2005
16
Fundus findings and longitudinal study of visual acuity loss in patients with X-linked retinoschisis. 25 61
16077359 2005
17
RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis. 61 25
15326152 2004
18
Expression of X-linked retinoschisis protein RS1 in photoreceptor and bipolar cells. 61 25
11222545 2001
19
Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene. 25 61
10922205 2000
20
Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave. 25 61
10458173 1999
21
Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis. The Retinoschisis Consortium. 25 61
9618178 1998
22
Identification of the retinoschisin-binding site on the retinal Na/K-ATPase. 25
31048931 2019
23
Intrafamilial Phenotype Variability in Two Male Siblings, With X-linked Juvenile Retinoschisis and Dorzolamide Treatment Effect in the Natural History of the Disease. 25
30923717 2019
24
X-linked juvenile retinoschisis (XLRS): a review of genotype-phenotype relationships. 25
24138048 2013
25
Foveal retinoschisis misdiagnosed as bilateral amblyopia. 25
22752678 2012
26
X-linked juvenile retinoschisis: clinical diagnosis, genetic analysis, and molecular mechanisms. 25
22245536 2012
27
Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisis. 25
16027044 2005
28
Peripheral retinal degenerations and the risk of retinal detachment. 25
12834683 2003
29
Japanese X-linked juvenile retinoschisis: conflict of phenotype and genotype with novel mutations in the XLRS1 gene. 25
11594966 2001
30
First molecular evidence for a de novo mutation in RS1 (XLRS1) associated with X linked juvenile retinoschisis. 25
10636740 1999
31
Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in Finland. 25
10234514 1999
32
Familial foveal retinoschisis associated with a rod-cone dystrophy. 25
306756 1978
33
Current Clinical Applications of In Vivo Gene Therapy with AAVs. 61
33309881 2021
34
Immune function in X-linked retinoschisis subjects in an AAV8-RS1 phase I/IIa gene therapy trial. 61
33601057 2021
35
A novel mutation in the RS1 gene in a Chinese family with X-linked congenital retinoschisis. 61
33335587 2021
36
Engineered FnCas12a with enhanced activity through directional evolution in human cells. 61
33567342 2021
37
Carbonic anhydrase inhibition in X-linked retinoschisis: An eye on the photoreceptors. 61
33186570 2021
38
Genetic Rescue of X-Linked Retinoschisis Mouse (Rs1-/y) Retina Induces Quiescence of the Retinal Microglial Inflammatory State Following AAV8-RS1 Gene Transfer and Identifies Gene Networks Underlying Retinal Recovery. 61
33019822 2020
39
Retinal detachment repair with perfluoro-N-octane endotamponade in an infant with juvenile X-linked retinoschisis. 61
33235941 2020
40
Surgical management of a large retinal cyst in X-linked retinoschisis with internal drainage: Report of an unusual case. 61
32971698 2020
41
Clinical manifestation and genetic analysis in Chinese early onset X-linked retinoschisis. 61
33460243 2020
42
Retinoschisis associated with Kearns-Sayre syndrome. 61
32787478 2020
43
HANDHELD SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY FINDINGS OF X-LINKED RETINOSCHISIS IN EARLY CHILDHOOD. 61
31764609 2020
44
Outcome measures in juvenile X-linked retinoschisis: A systematic review. 61
32313171 2020
45
Simplex Crumbs Homologue 1 Maculopathy Masquerading as Juvenile X-Linked Retinoschisis in Male Patients. 61
33029571 2020
46
Multimodal imaging of bilateral macular hole in X-linked retinoschisis. 61
32907874 2020
47
X-Linked Retinoschisis in Females in a Consanguineous Family: A Rare Entity 61
32854471 2020
48
The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies. 61
32860923 2020
49
A case of undiagnosed X-linked retinoschisis presenting as unilateral macular demarcation line. 61
32698614 2020
50
X-Linked Retinoschisis without Macular Retinoschisis: A New RS1 Mutation. 61
32646553 2020
51
Dramatic response to topical dorzolamide in X-linked retinoschisis. 61
32587200 2020
52
Full-Field Electroretinography, Pupillometry, and Luminance Thresholds in X-Linked Retinoschisis. 61
32579680 2020
53
Effectiveness of Ripasudil, a Rho-Associated Coiled/Coil-Containing Protein Kinase Inhibitor, in Improving Retinoschisis and Cystic-Like Foveal Cavities in Eyes with X-Linked Retinoschisis. 61
32999669 2020
54
Electronegative Electroretinograms in the United Arab Emirates. 61
32874040 2020
55
Unusual presentation of early-onset X-linked retinoschisis: Report after 1 year of multimodal follow-up. 61
32306756 2020
56
Retinal Detachment in X-Linked Retinoschisis. 61
32187471 2020
57
CRB1-Related Cystic Maculopathy in Twins Conceived Through Heterologous Fertilization With Variant-Carrying Oocytes. 61
32176805 2020
58
Adult Presentation of X-Linked Retinoschisis: Patient and Physician Perspectives. 61
32060879 2020
59
Effect of light and diurnal variation on macular thickness in X-linked retinoschisis: a case series. 61
31897705 2020
60
Establishment of a human induced pluripotent stem cell line (CSUASOi005-A), from peripheral blood mononuclear cells of a patient with X-linked juvenile retinoschisis carrying a novel mutation in RS1 gene. 61
32050117 2020
61
X-linked peripheral retinoschisis without macular involvement: a case series with RS1 genetic confirmation. 61
32124668 2020
62
Peripheral retinal neovascularization secondary to highly myopic superficial Retinoschisis: a case report. 61
31931752 2020
63
Acute Vitreous and Intraretinal Hemorrhage with Multifocal Subretinal Fluid in Juvenile X-Linked Retinoschisis. 61
33299625 2020
64
A Female Case of X-Linked Retinoschisis with Macular Hole Bilaterally. 61
32879744 2020
65
X-linked retinoschisis. 61
31856528 2020
66
Clinical findings and RS1 genotype in 90 Chinese families with X-linked retinoschisis. 61
32300273 2020
67
Carboxylated nanodiamond-mediated CRISPR-Cas9 delivery of human retinoschisis mutation into human iPSCs and mouse retina. 61
31672582 2020
68
The genetic aetiology of retinal degeneration in children in Finland - new founder mutations identified. 61
31087526 2019
69
Bilateral giant macular schisis in a case of Goldmann-Favre syndrome. 61
31558488 2019
70
CAPILLARY NETWORK ALTERATIONS IN X-LINKED RETINOSCHISIS IMAGED ON OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY. 61
29877903 2019
71
A case of X-linked retinoschisis with atypical fundus appearance. 61
31006083 2019
72
Efficacy of topical brinzolamide in children with retinal dystrophies. 61
31496370 2019
73
Molecular characterization of a rare phenotype of X-linked retinoschisis with angle-closure glaucoma. 61
31238476 2019
74
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function. 61
31149861 2019
75
A proposed mechanism influencing structural patterns in X-linked retinoschisis and stellate nonhereditary idiopathic foveomacular retinoschisis. 61
30518975 2019
76
Cryo-EM of retinoschisin branched networks suggests an intercellular adhesive scaffold in the retina. 61
30630865 2019
77
Wide-Field Swept-Source OCT and Angiography in X-Linked Retinoschisis. 61
31014769 2019
78
Overlapping retinal phenotypes in a consanguineous family harboring mutations in CRB1 and RS1. 61
30608181 2019
79
The Natural History of Congenital X-Linked Retinoschisis and Conversion between Phenotypes over Time. 61
30935660 2019
80
A Novel Pathogenic RS1 Variant (c.362delA) in a Korean Patient With Late-onset X-linked Retinoschisis. 61
30215241 2019
81
[Best's disease]. 61
31762926 2019
82
Prospective Evaluation of Patients With X-Linked Retinoschisis During 18 Months. 61
30551202 2018
83
Angio-OCT findings in juvenile X-linked retinoschisis. 61
29636197 2018
84
The treatment of refractory angle-closure glaucoma in a patient with X-linked juvenile retinoschisis. 61
30081704 2018
85
STRUCTURAL AND FUNCTIONAL MONITORING OF EXTRAMACULAR CYSTOID SPACES IN A CASE OF X-LINKED RETINOSCHISIS TREATED WITH ACETAZOLAMIDE. 61
27984356 2018
86
Optical Coherence Tomography Angiography Findings in X-Linked Retinoschisis. 61
30222815 2018
87
Long-term follow-up of a CRB1-associated maculopathy. 61
29869924 2018
88
SD-OCT AND MICROPERIMETRIC CORRELATED CHANGES IN PROGRESSIVE X-LINKED RETINOSCHISIS AFTER VITRECTOMY: A CASE REPORT. 61
27798534 2018
89
RETINAL DETACHMENT SURGERY IN A PEDIATRIC POPULATION: Visual and Anatomic Outcomes. 61
28858062 2018
90
ISCEV extended protocol for the photopic On-Off ERG. 61
29934802 2018
91
Analysis of Anatomic and Functional Measures in X-Linked Retinoschisis. 61
30025115 2018
92
Vitreous veils in X-linked retinoschisis. 61
29908649 2018
93
Gene therapy and genome surgery in the retina. 61
29856367 2018
94
Congenital X-Linked Retinoschisis: An Updated Clinical Review. 61
29633586 2018
95
Bullous X linked retinoschisis: clinical features and prognosis. 61
28848025 2018
96
Swept-source and optical coherence tomography angiography in patients with X-linked retinoschisis. 61
29303151 2018
97
Retinal vasproliferative tumor in a case of X-linked retinoschisis detachment. 61
29468219 2018
98
The diagnostic usefulness of the negative electroretinogram. 61
29198644 2018
99
Paradoxical Anatomic Response to Topical Carbonic Anhydrase Inhibitor in X-linked Retinoschisis. 61
29443366 2018
100
Understanding variable disease severity in X-linked retinoschisis: Does RS1 secretory mechanism determine disease severity? 61
29851975 2018
101
Gene therapy for inherited retinal and optic nerve degenerations. 61
29057663 2018
102
Clinical observations of vitreoretinal surgery for four different phenotypes of X-linked congenital retinoschisis. 61
29977812 2018
103
Peripheral fundus findings in X-linked retinoschisis. 61
28348004 2017
104
Long-term rearrangement of retinal structures in a novel mutation of X-linked retinoschisis. 61
28811895 2017
105
Nasal involvement in X-linked retinoschisis. 61
28820162 2017
106
USE OF A CARBONIC ANHYDRASE INHIBITOR IN X-LINKED RETINOSCHISIS: Effect on Cystic-Appearing Macular Lesions and Visual Acuity. 61
27828908 2017
107
Cystoid macular edema secondary to paclitaxel therapy for ovarian cancer: A case report. 61
28781803 2017
108
SURGICAL TREATMENT OF A MACULAR HOLE IN X-LINKED RETINOSCHISIS. 61
27203560 2017
109
Sustained Resolution of Macular Retinoschisis After Trabeculectomy in a Patient With Progressive Glaucoma. 61
28221332 2017
110
Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss. 61
28574807 2017
111
Juvenile Macular Degenerations. 61
28941524 2017
112
Clinical features of a toddler with bilateral bullous retinoschisis with a novel RS1 mutation. 61
29503952 2017
113
Prominent Optic Disc Featured in Inherited Retinopathy. 61
28147405 2017
114
Juvenile X-linked retinoschisis responsive to intravitreal corticosteroids. 61
29503947 2017
115
Juvenile X-linked retinoschisis presenting as juxtapapillary retinal fold mimicking combined hamartoma of the retina and retinal pigment epithelium. 61
28147237 2017
116
Genetic analysis and clinical features of X-linked retinoschisis in Chinese patients. 61
28272453 2017
117
Rearing Light Intensity Affects Inner Retinal Pathology in a Mouse Model of X-Linked Retinoschisis but Does Not Alter Gene Therapy Outcome. 61
28297725 2017
118
Case report of an atypical early onset X-linked retinoschisis in monozygotic twins. 61
28235399 2017
119
[Swept-Source optical coherence tomography angiography of X-linked retinoschisis]. 61
28081919 2017
120
X-Linked Retinoschisis in Juveniles: Follow-Up by Optical Coherence Tomography. 61
28286756 2017
121
The Role of Gene Therapy in the Treatment of Retinal Diseases: A Review. 61
29149824 2017
122
Proteomic profiling of human intraschisis cavity fluid. 61
28450823 2017
123
Retinal Detachment in a Combined Case of Stickler Syndrome and X-Linked Retinoschisis. 61
28060400 2017
124
Outer Plexiform Layer Structures Are Not Altered Following AAV-Mediated Gene Transfer in Healthy Rat Retina. 61
28280483 2017
125
[Do We Still Need Electrophysiology in Ophthalmology?] 61
27984836 2016
126
Gene and cell-based therapies for inherited retinal disorders: An update. 61
27862925 2016
127
Structural analysis of X-linked retinoschisis mutations reveals distinct classes which differentially effect retinoschisin function. 61
27798099 2016
128
Juvenile X-Linked Retinoschisis: A Comparison of Imaging Modalities and Review of Angiographic Findings. 61
27164547 2016
129
Mizuo-Nakamura Phenomena. 61
27842204 2016
130
Immediate Sequential Bilateral Pediatric Vitreoretinal Surgery: An International Multicenter Study. 61
27221737 2016
131
Abnormal 8-Hz flicker electroretinograms in carriers of X-linked retinoschisis. 61
27369766 2016
132
Phenotypic characterization of X-linked retinoschisis: Clinical, electroretinography, and optical coherence tomography variables. 61
27609164 2016
133
Retinal Structure and Gene Therapy Outcome in Retinoschisin-Deficient Mice Assessed by Spectral-Domain Optical Coherence Tomography. 61
27409484 2016
134
Dramatic regression of macular and peripheral retinoschisis with dorzolamide 2 % in X-linked retinoschisis: a case report. 61
27246168 2016
135
WIDE-FIELD IMAGING OF NONEXUDATIVE AND EXUDATIVE CONGENITAL X-LINKED RETINOSCHISIS. 61
26655612 2016
136
Lamellar macular hole in X linked retinoschisis. 61
27170611 2016
137
Preclinical Dose-Escalation Study of Intravitreal AAV-RS1 Gene Therapy in a Mouse Model of X-linked Retinoschisis: Dose-Dependent Expression and Improved Retinal Structure and Function. 61
27036983 2016
138
Paired octamer rings of retinoschisin suggest a junctional model for cell-cell adhesion in the retina. 61
27114531 2016
139
Corrigendum: X-Linked Retinoschisis: Phenotypic Variability in a Chinese Family. 61
26960251 2016
140
Comments on temporary resolution of foveal schisis following vitrectomy with silicon oil tamponade in X-linked retinoschisis with retinal detachment. 61
27146945 2016
141
Unilateral giant peripapillary drusen and retinal drusenoid deposits in a case of X-linked retinoschisis. 61
26907824 2016
142
Structure/Psychophysical Relationships in X-Linked Retinoschisis. 61
26830370 2016
143
Cog-Wheel Octameric Structure of RS1, the Discoidin Domain Containing Retinal Protein Associated with X-Linked Retinoschisis. 61
26812435 2016
144
X-Linked Retinoschisis: Phenotypic Variability in a Chinese Family. 61
26823236 2016
145
X-Linked retinoschisis associated to a novel intragenic microdeletion: case report. 61
26791414 2016
146
Rebound macular edema following oral acetazolamide therapy for juvenile X-linked retinoschisis in an Italian family. 61
27932860 2016
147
An ex vivo gene therapy approach in X-linked retinoschisis. 61
27390514 2016
148
Swept-Source Optical Coherence Tomography Angiography of Paediatric Macular Diseases. 61
27023179 2016
149
[Gene Therapy for Inherited RETINAL AND OPTIC NERVE Disorders: Current Knowledge]. 61
27860478 2016
150
Ocular and systemic safety of a recombinant AAV8 vector for X-linked retinoschisis gene therapy: GLP studies in rabbits and Rs1-KO mice. 61
27626041 2016
151
[Preimplantation genetic diagnosis and monogenic inherited eye diseases]. 61
28224801 2016
152
The best of the best: a review of select retina case reports published in 2015. 61
28924409 2016
153
Temporary resolution of foveal schisis following vitrectomy with silicon oil tamponade in X-linked retinoschisis with retinal detachment. 61
26669343 2015
154
[OCT findings in X-linked retinoschisis]. 61
26025031 2015
155
Clinical and molecular characterization of females affected by X-linked retinoschisis. 61
25894957 2015
156
A novel gene mutation in a family with X-linked retinoschisis. 61
24529551 2015
157
Safety and Biodistribution Evaluation of rAAV2tYF-CB-hRS1, a Recombinant Adeno-Associated Virus Vector Expressing Retinoschisin, in RS1-Deficient Mice. 61
26390091 2015
158
Safety and Biodistribution Evaluation in Cynomolgus Macaques of rAAV2tYF-CB-hRS1, a Recombinant Adeno-Associated Virus Vector Expressing Retinoschisin. 61
26390090 2015
159
Vitreous Veils Associated With Congenital X-Linked Retinoschisis. 61
26270406 2015
160
Synaptic pathology and therapeutic repair in adult retinoschisis mouse by AAV-RS1 transfer. 61
26098217 2015
161
Restoration of synaptic function in sight for degenerative retinal disease. 61
26098210 2015
162
The gene mutation in a Taiwanese family with X-linked retinoschisis. 61
26043410 2015
163
Resolution of foveal schisis in X-linked retinoschisis in the setting of retinal detachment. 61
25892045 2015
164
Detailed Morphological Changes of Foveoschisis in Patient with X-Linked Retinoschisis Detected by SD-OCT and Adaptive Optics Fundus Camera. 61
26356828 2015
165
Clinical presentations of X-linked retinoschisis in Taiwanese patients confirmed with genetic sequencing. 61
25999676 2015
166
Ocriplasmin for foveal schisis in X-linked retinoschisis. 61
26002140 2015
167
Preclinical safety evaluation of a recombinant AAV8 vector for X-linked retinoschisis after intravitreal administration in rabbits. 61
25211193 2014
168
X-linked juvenile retinoschisis in a consanguineous family: phenotypic variability and report of a homozygous female patient. 61
25054456 2014
169
Test-Retest Intervisit Variability of Functional and Structural Parameters in X-Linked Retinoschisis. 61
25346871 2014
170
Optical coherence tomography retinal thickness and volume measurements in X-linked retinoschisis. 61
24879947 2014
171
A combination of topical and systemic carbonic anhydrase in the treatment of chromosome X-linked retinoschisis. 61
24269421 2014
172
Retinoschisis and hyperopia associated with partial monosomy of 6q and partial trisomy of 11q. 61
24251586 2014
173
Resolution of mid-peripheral schisis in x-linked retinoschisis with the use of dorzolamide. 61
23514609 2014
174
Retinoschisin gene therapy in photoreceptors, Müller glia or all retinal cells in the Rs1h-/- mouse. 61
24694538 2014
175
Correlation between spectral-domain OCT findings and visual acuity in X-linked retinoschisis. 61
24713485 2014
176
Photoreceptor pathology in the X-linked retinoschisis (XLRS) mouse results in delayed rod maturation and impaired light driven transducin translocation. 61
24664744 2014
177
X-linked retinoschisis--clinical manifestation, genetic and electrophysiological analysis of three generations with p.Arg197Cys mutation of RS1 gene. 61
25799783 2014
178
Novel mutations of the RS1 gene in a cohort of Chinese families with X-linked retinoschisis. 61
24505212 2014
179
Juvenile-onset macular degeneration and allied disorders. 61
24732760 2014
180
Posterior subtenon injection of triamcinolone acetonide after phacoemulsification in a patient with X-linked retinoschisis. 61
23974665 2013
181
Macular hole in juvenile X-linked retinoschisis. 61
24409088 2013
182
Hereditary retinal eye diseases in childhood and youth affecting the central retina. 61
24391367 2013
183
[Paediatric retinal detachment and hereditary vitreoretinal disorders]. 61
23986190 2013
184
Vitrectomy for X-linked retinoschisis: a case report and literature review. 61
23931486 2013
185
Macular drusenoid deposits in X-linked retinoschisis. 61
23896453 2013
186
A phenotype-genotype correlation study of X-linked retinoschisis. 61
23453514 2013
187
Automated segmentation of pathological cavities in optical coherence tomography scans. 61
23737469 2013
188
In vivo-directed evolution of a new adeno-associated virus for therapeutic outer retinal gene delivery from the vitreous. 61
23761039 2013
189
Topical brinzolamide for foveal schisis in juvenile retinoschisis. 61
23541677 2013
190
[Detection and prenatal diagnosis for RS1 gene mutations in two Chinese families with X-linked juvenile retinoschisis]. 61
23568735 2013
191
[Significance of ophthalmological imaging in common hereditary retinal diseases]. 61
23229225 2013
192
Microplasmin (ocriplasmin) in pediatric vitreoretinal surgery: update and review. 61
23001068 2013
193
Characterization of novel RS1 exonic deletions in juvenile X-linked retinoschisis. 61
24227916 2013
194
X-linked juvenile retinoschisis in females and response to carbonic anhydrase inhibitors: case report and review of the literature. 61
23163265 2013
195
[A case of clinical manifestation of X-linked retinoschisis--in the one eye, and choroidal neovascularisation--in the second eye, in two family members]. 61
24059032 2013
196
Wide-field spectral-domain optical coherence tomography in patients and carriers of X-linked retinoschisis. 61
23009889 2013
197
Optical Coherence Tomography evaluation in X-linked retinoschisis. 61
23138727 2012
198
Loss of retinoschisin (RS1) cell surface protein in maturing mouse rod photoreceptors elevates the luminance threshold for light-driven translocation of transducin but not arrestin. 61
22993419 2012
199
Long-term outcomes of vitrectomy for progressive X-linked retinoschisis. 61
22541657 2012
200
Evaluation of focal retinal function using multifocal electroretinography in patients with x-linked retinoschisis (CJO Vol. 45, No. 5). 61
22560431 2012
201
Novel RS1 mutations associated with X-linked juvenile retinoschisis. 61
22245991 2012
202
Mutations in the RS1 gene in a Chinese family with X-linked juvenile retinoschisis. 61
25343070 2012
203
Novel clinical manifestation of congenital X-linked retinoschisis. 61
22332228 2012
204
Negative electroretinograms in the pediatric and adult population. 61
22246197 2012
205
In silico investigation of the disease-associated retinoschisin C110Y and C219G mutants. 61
22292953 2012
206
Four novel RS1 gene mutations in Polish patients with X-linked juvenile retinoschisis. 61
23288992 2012
207
Scanning laser ophthalmoscope retro-mode imaging of foveal schisis in eyes with X-linked retinoschisis. 61
21902790 2012
208
Two cases of X-linked retinoschisis with different spectral domain optical coherence tomography findings. 61
23055679 2012
209
Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene. 61
22110067 2011
210
Bilateral macular holes in X-linked retinoschisis: now the spectrum is wider. 61
22011501 2011
211
[X linked retinoschisis, unusual presentation: strabismus]. 61
22004578 2011
212
Macular cysts in retinal dystrophy. 61
21730849 2011
213
Phenotypic expression of X-linked retinoschisis in Chinese families with mutations in the RS1 gene. 61
21701876 2011
214
X-linked retinoschisis maculopathy treated with topical dorzolamide, and relationship to genotype. 61
21527955 2011
215
Effect of aging on macular features of X-linked retinoschisis assessed with optical coherence tomography. 61
21386765 2011
216
Combined external drainage and 25-gauge vitrectomy for severe X-linked congenital retinoschisis. 61
21836411 2011
217
The use of carbonic anhydrase inhibitors in the retreatment of cystic macular lesions in retinitis pigmentosa and X-linked retinoschisis. 61
20966823 2011
218
Report of two brothers with short stature, microcephaly, mental retardation, and retinoschisis-A new mental retardation syndrome? 61
21204205 2011
219
Regulation of retinoschisin secretion in Weri-Rb1 cells by the F-actin and microtubule cytoskeleton. 61
21738583 2011
220
Tyrosinase is the modifier of retinoschisis in mice. 61
20876567 2010
221
Molecular mechanisms leading to null-protein product from retinoschisin (RS1) signal-sequence mutants in X-linked retinoschisis (XLRS) disease. 61
20809529 2010
222
Evaluation of focal retinal function using multifocal electroretinography in patients with X-linked retinoschisis. 61
20648073 2010
223
Long-term 12 year follow-up of X-linked congenital retinoschisis. 61
20569020 2010
224
Spontaneous resolution of foveal cysts associated with X-linked retinoschisis as observed by optical coherence tomography. 61
20648079 2010
225
Retinoschisin (RS1) interacts with negatively charged lipid bilayers in the presence of Ca2+: an atomic force microscopy study. 61
20677810 2010
226
Nidek MP-1 microperimetry and Fourier domain optical coherence tomography (FD-OCT) in X linked retinoschisis. 61
20606028 2010
227
Foveomacular schisis in juvenile X-linked retinoschisis: an optical coherence tomography study. 61
20430364 2010
228
Diagnosis and pathogenesis of congenital X-linked retinoschisis with optical coherence tomography. 61
20349904 2010
229
Extended Endotamponade with Perfluoro-n-Octane in Pediatric Retinal Detachment. 61
20337323 2010
230
Efficacy of sustained topical dorzolamide therapy for cystic macular lesions in patients with X-linked retinoschisis. 61
20142541 2010
231
Genotypic analysis of X-linked retinoschisis in Western Australia. 61
20238027 2010
232
An unusual fundus phenotype of inner retinal sheen in X-linked retinoschisis. 61
19741719 2009
233
An audit of genetic testing in diagnosis of inherited retinal disorders: a prerequisite for gene-specific intervention. 61
19788668 2009
234
The effects of transient retinal detachment on cavity size and glial and neural remodeling in a mouse model of X-linked retinoschisis. 61
19387072 2009
235
Foveal schisis with Mizuo phenomenon: etio-pathogenesis of tapetal reflex in X-linked retinoschisis. 61
18535589 2009
236
Retinal nerve fibre layer thickness analysis in X-linked retinoschisis using Fourier-domain OCT. 61
19373267 2009
237
[Macular edema without fluorescein leakeage]. 61
19769867 2009
238
Macular spectral-domain optical coherence tomography in patients with X linked retinoschisis. 61
19019942 2009
239
Treatment of adult-onset acute macular retinoschisis in enhanced s-cone syndrome with oral acetazolamide. 61
18835469 2009
240
Relation of response to treatment with dorzolamide in X-linked retinoschisis to the mechanism of functional loss in retinoschisin. 61
18834580 2009
241
Spectral-domain OCT and microperimeter characterization of morphological and functional changes in X-linked retinoschisis. 61
19205503 2009
242
Congenital x-linked retinoschisis: a novel approach for management of a large schitic cavity overhanging the macula. 61
25390856 2009
243
Vitreoretinal surgery without schisis cavity excision for the management of juvenile X linked retinoschisis. 61
18952658 2008
244
Characterization and purification of the discoidin domain-containing protein retinoschisin and its interaction with galactose. 61
18690710 2008
245
Retinal morphological changes of patients with X-linked retinoschisis evaluated by Fourier-domain optical coherence tomography. 61
18541843 2008
246
Preimplantation genetic diagnosis of X-linked retinoschisis. 61
18549702 2008
247
X-linked retinoschisis. 61
18452772 2008
248
Hereditary retinal disease. 61
18408503 2008
249
Detection of mosaic retinal dysfunction in choroideremia carriers electroretinographic and psychophysical testing. 61
18201765 2008
250
Resolution of retinoschisis after vitreous surgery in X-linked retinoschisis. 61
17854899 2008
251
Genetic modification of the schisis phenotype in a mouse model of X-linked retinoschisis. 61
18245825 2008
252
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update. 61
17985165 2008
253
Retinoschisin (RS1), the protein encoded by the X-linked retinoschisis gene, is anchored to the surface of retinal photoreceptor and bipolar cells through its interactions with a Na/K ATPase-SARM1 complex. 61
17804407 2007
254
Elevated levels of cystatin C and tenascin-C in schisis cavities of patients with congenital X-linked retinoschisis. 61
18040250 2007
255
Plasmin enzyme-assisted vitreoretinal surgery in congenital X-linked retinoschisis: surgical techniques based on a new classification system. 61
18040249 2007
256
Unusual manifestations of x-linked retinoschisis: clinical profile and diagnostic evaluation. 61
17631851 2007
257
Macular and extramacular optical coherence tomography findings in X-linked retinoschisis. 61
17955851 2007
258
Coexpression and interaction of wild-type and missense RS1 mutants associated with X-linked retinoschisis: its relevance to gene therapy. 61
17525175 2007
259
X-linked retinoschisis: an update. 61
17172462 2007
260
Genetic variations in the hotspot region of RS1 gene in Indian patients with juvenile X-linked retinoschisis. 61
17515881 2007
261
Acetazolamide in the treatment of X-linked retinoschisis maculopathy. 61
17420384 2007
262
Peripapillary schisis in glaucoma patients with narrow angles and increased intraocular pressure. 61
17386284 2007
263
X-linked retinoschisis in a female with a heterozygous RS1 missense mutation. 61
17304551 2007
264
Novel phenotypic and genotypic findings in X-linked retinoschisis. 61
17296904 2007
265
Multifocal ERG findings in carriers of X-linked retinoschisis. 61
17180613 2007
266
Macular hole secondary to X-linked retinoschisis. 61
16628241 2006
267
Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram. 61
16612636 2006
268
Reduced synaptic vesicle density and aberrant synaptic localization caused by a splice site mutation in the Rs1h gene. 61
17266781 2006
269
X-linked retinoschisis: novel mutation in the initiation codon of the XLRS1 gene in a large family. 61
17031297 2006
270
An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation. 61
16884758 2006
271
Congenital X-linked retinoschisis classification system. 61
16946682 2006
272
Use of dorzolamide for patients with X-linked retinoschisis. 61
16963845 2006
273
Intraschisis cavity fluid composition in congenital X-linked retinoschisis. 61
16946681 2006
274
Retinoschisin expression and localization in rodent and human pineal and consequences of mouse RS1 gene knockout. 61
17093404 2006
275
Bilateral macular detachments in X-linked retinoschisis. 61
16832033 2006
276
A novel mutation in the XLRS1 gene in a Korean family with X-linked retinoschisis. 61
16768192 2006
277
Vitreous hemorrhage as the initial manifestation of X-linked retinoschisis in a 9-month-old infant. 61
16491731 2006
278
Molecular pathology of X linked retinoschisis: mutations interfere with retinoschisin secretion and oligomerisation. 61
16361673 2006
279
Fundus autofluorescence in children and teenagers with hereditary retinal diseases. 61
16034607 2006
280
Disease mechanisms and gene therapy in a mouse model for X-linked retinoschisis. 61
17249585 2006
281
[Importance of family examination in juvenile X-linked retinoschisis]. 61
15349747 2005
282
Retinal changes in juvenile X linked retinoschisis using three dimensional optical coherence tomography. 61
16299154 2005
283
Indocyanine green angiography of juvenile X-linked retinoschisis. 61
16139020 2005
284
Characteristics of contrast processing deficits in X-linked retinoschisis. 61
15845241 2005
285
An ENU-induced mutation in Rs1h causes disruption of retinal structure and function. 61
16088326 2005
286
Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia. 61
15932525 2005
287
X-linked retinoschisis: clinical phenotype and RS1 genotype in 86 UK patients. 61
15937075 2005
288
Foveal schisis as a cause of retinal detachment secondary to macular hole in juvenile X-linked retinoschisis. 61
15805920 2005
289
RS1, a discoidin domain-containing retinal cell adhesion protein associated with X-linked retinoschisis, exists as a novel disulfide-linked octamer. 61
15644328 2005
290
Correlation of optical coherence tomography findings with visual acuity and macular lesions in patients with X-linked retinoschisis. 61
15745780 2005
291
X-linked retinoschisis in three females from the same family: a phenotype-genotype correlation. 61
15655444 2005
292
A retinal neuronal developmental wave of retinoschisin expression begins in ganglion cells during layer formation. 61
15326155 2004
293
Two cases of X-linked juvenile retinoschisis with different optical coherence tomography findings and RS1 gene mutations. 61
15281981 2004
294
Optical coherence tomography in the diagnosis of juvenile X-linked retinoschisis. 61
15043546 2004
295
X-linked retinoschisis: a clinical and molecular genetic review. 61
14998693 2004
296
Optical coherence tomography of X-linked retinoschisis. 61
15076957 2004
297
Development of a large macular fold following surgical repair of a traction retinal detachment in a child with x-linked retinoschisis. 61
14707837 2003
298
Multifocal electroretinograms in X-linked retinoschisis. 61
14578418 2003
299
Consanguineous marriage resulting in homozygous occurrence of X-linked retinoschisis in girls. 61
14516833 2003
300
X-Linked Congenital Retinoschisis 61
20301401 2003
301
A case of X-linked retinoschisis diagnosed in an infant. 61
14574272 2003
302
Retinal detachment 7 years after prophylactic schisis cavity excision in juvenile X-linked retinoschisis. 61
14509466 2003
303
Abnormalities of the scotopic threshold response correlated with gene mutation in X-linked retinoschisis and congenital stationary night blindness. 61
14661905 2003
304
X-linked retinoschisis: report of a family with a rare deletion in the XLRS1 gene. 61
12967815 2003
305
[Macular dystrophies]. 61
13130265 2003
306
Defective discoidin domain structure, subunit assembly, and endoplasmic reticulum processing of retinoschisin are primary mechanisms responsible for X-linked retinoschisis. 61
12746437 2003
307
Intracellular retention of mutant retinoschisin is the pathological mechanism underlying X-linked retinoschisis. 61
12417531 2002
308
Selective reduction of S-cone response and on-response in the cone electroretinograms of patients with X-linked retinoschisis. 61
12107512 2002
309
Analysis of photoreceptor function and inner retinal activity in juvenile X-linked retinoschisis. 61
11738458 2001
310
[Pseudohypopyon of cholesterol crystals occurring 16 years after retinal detachment in x-linked retinoschisis]. 61
11731903 2001
311
Understanding human disease mutations through the use of interspecific genetic variation. 61
11689479 2001
312
High-frequency attenuation of the cone ERG and ON-response deficits in X-linked retinoschisis. 61
11481277 2001
313
Axial length and refractive error in X-linked retinoschisis. 61
11384589 2001
314
[Identification of mutation of the X-linked juvenile retinoschisis gene]. 61
11295123 2001
315
Origin of deficits in the flicker electroretinogram of the cone system in X-linked retinoschisis as derived from response nonlinearities. 61
11318324 2001
316
On-response deficit in the electroretinogram of the cone system in X-linked retinoschisis. 61
11157882 2001
317
Foveal ectopia in X-linked retinoschisis. 61
11508883 2001
318
[Bullous form of X-linked congenital retinoschisis in infants]. 61
11339042 2001
319
Retinoschisin, the X-linked retinoschisis protein, is a secreted photoreceptor protein, and is expressed and released by Weri-Rb1 cells. 61
10915776 2000
320
Unilateral macular retinoschisis with stellate foveal appearance in two females with myopia. 61
10847501 2000
321
X-linked retinoschisis with point mutations in the XLRS1 gene. 61
10636421 2000
322
Clinical phenotype associated with the arg141 his mutation in the X-linked retinoschisis gene. 61
10636429 2000
323
Histopathological findings of X-linked retinoschisis with neovascular glaucoma. 61
10664045 2000
324
Temporal frequency deficits in the electroretinogram of the cone system in X-linked retinoschisis. 61
10960656 2000
325
Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis. 61
10576992 1999
326
Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis. 61
10453744 1999
327
Recurrent missense (R197C) and nonsense (Y89X) mutations in the XLRS1 gene in families with X-linked retinoschisis. 61
10079181 1999
328
A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutation. 61
10415464 1999
329
The use of perfluorodecalin in retinal detachments with retinoschisis. 61
9793947 1998
330
[Hereditary macular dystrophies]. 61
9793380 1998
331
Novel mutations in the XLRS1 gene may be caused by early Okazaki fragment sequence replacement. 61
9699564 1998
332
Optical cross-sectional imaging of the macula with the retinal thickness analyzer in X-linked retinoschisis. 61
9715684 1998
333
The natural history of X-linked retinoschisis. 61
9606571 1998
334
Exudative retinal detachment in X-linked retinoschisis. 61
9571668 1998
335
Outcomes of vitreoretinal surgery in patients with X-linked retinoschisis. 61
9547772 1998
336
High-resolution physical map of the X-linked retinoschisis interval in Xp22. 61
9325051 1997
337
High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes. 61
9195994 1997
338
Linkage mapping of a large Colombian family segregating for X linked retinoschisis: refinement of the chromosomal location. 61
9192273 1997
339
Improved genetic mapping of X linked retinoschisis. 61
8950671 1996
340
Use of perfluorocarbon liquid in the repair of retinoschisis retinal detachments. 61
8878197 1996
341
Clinical features in affected males with X-linked retinoschisis. 61
8600886 1996
342
Linkage mapping of new X-linked juvenile retinoschisis kindreds using microsatellite markers. 61
8607849 1996
343
Electroretinographic findings in macular dystrophy. 61
9476599 1996
344
X linked retinoschisis. 61
7662639 1995
345
Infantile presentation of X linked retinoschisis. 61
7662629 1995
346
Refined genetic mapping of juvenile X-linked retinoschisis. 61
7558052 1995
347
Postreceptoral contribution to macular dysfunction in retinitis pigmentosa. 61
8002248 1994
348
Surgical management of complications associated with X-linked retinoschisis. 61
8352691 1993
349
Cone dystrophies with negative photopic electroretinogram. 61
8343466 1993
350
Focal macular electroretinogram in X-linked congenital retinoschisis. 61
8449671 1993
351
Retinal angioma and juvenile sex-linked retinoschisis. 61
1495769 1992
352
Mizuo phenomenon in X-linked retinoschisis. Pathogenesis of the Mizuo phenomenon. 61
1867553 1991
353
Contribution to carrier detection and genetic counselling in X linked retinoschisis. 61
1678432 1991
354
Male proband with X linked retinoschisis apparently inherited from his father's family. 61
2051461 1991
355
Nasal retinal dragging in X-linked retinoschisis. 61
1916317 1991
356
Follow-up study of X-linked retinoschisis. 61
1937084 1991
357
Posthumous diagnosis of X-linked retinoschisis using DNA analysis. 61
1982897 1990
358
Progressive retinal changes observed in juvenile X-linked retinoschisis. 61
2380473 1990
359
[Prenatal diagnosis of various hereditary blinding diseases]. 61
2250955 1990
360
X-linked congenital retinoschisis. 61
2227486 1990
361
[X-chromosomal congenital retinoschisis. Clinical aspects and electrophysiology]. 61
2376375 1990
362
Unusual manifestations of X-linked retinoschisis. 61
2095022 1990
363
[AC and DC electroretinography in degenerative retinal diseases]. 61
2358278 1990
364
Linkage relationships and gene order around the locus for X-linked retinoschisis. 61
3177388 1988
365
Detection of the carrier state of X-linked retinoschisis. 61
3377039 1988
366
DNA linkage analysis of X-linked retinoschisis. 61
2894345 1988
367
X-linked retinoschisis and linkage. 61
3359666 1988
368
X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85. 61
2887320 1987
369
Hereditary X-linked retinoschisis and bilateral congenital retinal detachment. 61
3602602 1987
370
Congenital hereditary (juvenile X-linked) retinoschisis. Histopathologic and ultrastructural findings in three eyes. 61
3954665 1986
371
The C-wave in hereditary degenerations of the ocular fundus. 61
4042819 1985
372
Rod-cone interactions and analysis of retinal disease. 61
3873959 1985
373
Vascular opacification and leakage in X-linked (juvenile) retinoschisis. 61
572698 1979
374
[Clinical and electroophthalmologic findings in x-chromosomal juvenile retinoschisis]. 61
422116 1979

Variations for X-Linked Congenital Retinoschisis

Expression for X-Linked Congenital Retinoschisis

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Pathways for X-Linked Congenital Retinoschisis

GO Terms for X-Linked Congenital Retinoschisis

Sources for X-Linked Congenital Retinoschisis

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