These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 34828422)

  • 21. Clinical and genetic features of retinoschisis in 120 families with
    Xiao S; Sun W; Xiao X; Li S; Luo H; Jia X; Ouyang J; Li X; Wang Y; Jiang Y; Wang P; Zhang Q
    Br J Ophthalmol; 2023 Mar; 107(3):367-372. PubMed ID: 34645606
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Overlapping retinal phenotypes in a consanguineous family harboring mutations in CRB1 and RS1.
    Khan AO; El-Ghrably IA
    Ophthalmic Genet; 2019 Feb; 40(1):17-21. PubMed ID: 30608181
    [TBL] [Abstract][Full Text] [Related]  

  • 23. X-Linked Retinoschisis: Phenotypic Variability in a Chinese Family.
    Xiao Y; Liu X; Tang L; Wang X; Coursey TG; Guo X; Li Z
    Sci Rep; 2016 Jan; 6():20118. PubMed ID: 26823236
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia.
    Hewitt AW; FitzGerald LM; Scotter LW; Mulhall LE; McKay JD; Mackey DA
    Clin Exp Ophthalmol; 2005 Jun; 33(3):233-9. PubMed ID: 15932525
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Multimodal imaging in a pedigree of X-linked Retinoschisis with a novel RS1 variant.
    Stephenson K; Dockery A; Wynne N; Carrigan M; Kenna P; Jane Farrar G; Keegan D
    BMC Med Genet; 2018 Nov; 19(1):195. PubMed ID: 30419843
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and molecular characterization of females affected by X-linked retinoschisis.
    Staffieri SE; Rose L; Chang A; De Roach JN; McLaren TL; Mackey DA; Hewitt AW; Lamey TM
    Clin Exp Ophthalmol; 2015; 43(7):643-7. PubMed ID: 25894957
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Rebound macular edema following oral acetazolamide therapy for juvenile X-linked retinoschisis in an Italian family.
    Galantuomo MS; Fossarello M; Cuccu A; Farci R; Preising MN; Lorenz B; Napoli PE
    Clin Ophthalmol; 2016; 10():2377-2382. PubMed ID: 27932860
    [TBL] [Abstract][Full Text] [Related]  

  • 28. In vivo imaging reveals novel aspects of retinal disease progression in Rs1h(-/Y) mice but no therapeutic effect of carbonic anhydrase inhibition.
    Zhour A; Bolz S; Grimm C; Willmann G; Schatz A; Weber BH; Zrenner E; Fischer MD
    Vet Ophthalmol; 2012 Sep; 15 Suppl 2():123-33. PubMed ID: 22672048
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular genetic characteristics of X-linked retinoschisis in Koreans.
    Kim SY; Ko HS; Yu YS; Hwang JM; Lee JJ; Kim SY; Kim JY; Seong MW; Park KH; Park SS
    Mol Vis; 2009; 15():833-43. PubMed ID: 19390641
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular characterization of a rare phenotype of X-linked retinoschisis with angle-closure glaucoma.
    Selvan H; Sharma A; Birla S; Gupta S; Somarajan BI; Gupta V; Sharma A
    Indian J Ophthalmol; 2019 Jul; 67(7):1226-1229. PubMed ID: 31238476
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical manifestation and genetic analysis in Chinese early onset X-linked retinoschisis.
    Huang L; Sun L; Wang Z; Chen C; Wang P; Sun W; Luo X; Ding X
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1421. PubMed ID: 33460243
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Correlation of genetic and clinical findings in Spanish patients with X-linked juvenile retinoschisis.
    Riveiro-Alvarez R; Trujillo-Tiebas MJ; Gimenez-Pardo A; Garcia-Hoyos M; Lopez-Martinez MA; Aguirre-Lamban J; Garcia-Sandoval B; Vazquez-Fernandez del Pozo S; Cantalapiedra D; Avila-Fernandez A; Baiget M; Ramos C; Ayuso C
    Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4342-50. PubMed ID: 19324861
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A Carrier Female Manifesting an Unusual X-Linked Retinoschisis Phenotype Associated with the Pathogenic Variant c.266delA, p.(Tyr89LeufsTer37) in
    Kirkby J; Halford S; Shanks M; Moore A; Gait A; Jenkins L; Clouston P; Patel CK; Downes SM
    Genes (Basel); 2023 May; 14(6):. PubMed ID: 37372373
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene.
    Duncan JL; Ratnam K; Birch DG; Sundquist SM; Lucero AS; Zhang Y; Meltzer M; Smaoui N; Roorda A
    Invest Ophthalmol Vis Sci; 2011 Dec; 52(13):9614-23. PubMed ID: 22110067
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The gene mutation in a Taiwanese family with X-linked retinoschisis.
    Huang CT; Chen SP; Tsai RK
    Kaohsiung J Med Sci; 2015 Jun; 31(6):309-14. PubMed ID: 26043410
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Phenotype Heterogeneity and the Association Between Visual Acuity and Outer Retinal Structure in a Cohort of Chinese X-Linked Juvenile Retinoschisis Patients.
    Guo Q; Li Y; Li J; You Y; Liu C; Chen K; Li S; Lei B
    Front Genet; 2022; 13():832814. PubMed ID: 35309139
    [No Abstract]   [Full Text] [Related]  

  • 37. Genotype and phenotype characteristics of X-linked retinoschisis: the first report of a Turkish population.
    Cetin GO; Cetin EN; Akyol T; Ilhan HD; Pekel G
    Ophthalmic Genet; 2022 Jun; 43(3):318-325. PubMed ID: 34865595
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Case report of an atypical early onset X-linked retinoschisis in monozygotic twins.
    Murro V; Caputo R; Bacci GM; Sodi A; Mucciolo DP; Bargiacchi S; Giglio SR; Virgili G; Rizzo S
    BMC Ophthalmol; 2017 Feb; 17(1):19. PubMed ID: 28235399
    [TBL] [Abstract][Full Text] [Related]  

  • 39. STELLATE NONHEREDITARY IDIOPATHIC FOVEOMACULAR RETINOSCHISIS: RESPONSE TO TOPICAL DORZOLAMIDE THERAPY.
    Ajlan RS; Hammamji KS
    Retin Cases Brief Rep; 2019; 13(4):364-366. PubMed ID: 28557864
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss.
    Sudha D; Patric IRP; Ganapathy A; Agarwal S; Krishna S; Neriyanuri S; Sripriya S; Sen P; Chidambaram S; Arunachalam JP
    Ophthalmic Genet; 2017; 38(3):260-266. PubMed ID: 28574807
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.