Lyons CJ - Search Results

1

Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region.

Ye XC, Roslin NM, Paterson AD, Lyons CJ, Pegado V, Richmond P, Shyr C, Fornes O, Han X, Higginson M, Ross CJ, Giaschi D, Gregory-Evans C, Patel MS, Wasserman WW. Ye XC, et al. Among authors: lyons cj. J Med Genet. 2022 Jan;59(1):46-55. doi: 10.1136/jmedgenet-2020-107226. Epub 2020 Nov 30. J Med Genet. 2022. PMID: 33257509 Free PMC article.

2

Correlation of novel PAX6 gene abnormalities in aniridia and clinical presentation.

Sannan NS, Gregory-Evans CY, Lyons CJ, Lehman AM, Langlois S, Warner SJ, Zakrzewski H, Gregory-Evans K. Sannan NS, et al. Among authors: lyons cj. Can J Ophthalmol. 2017 Dec;52(6):570-577. doi: 10.1016/j.jcjo.2017.04.006. Epub 2017 Jul 6. Can J Ophthalmol. 2017. PMID: 29217025

3

Sparing of coarse stereopsis in stereodeficient children with a history of amblyopia.

Giaschi D, Lo R, Narasimhan S, Lyons C, Wilcox LM. Giaschi D, et al. J Vis. 2013 Aug 28;13(10):17. doi: 10.1167/13.10.17. J Vis. 2013. PMID: 23986537 Free article.

4

Reading ability of children treated for amblyopia.

Kugathasan L, Partanen M, Chu V, Lyons C, Giaschi D. Kugathasan L, et al. Vision Res. 2019 Mar;156:28-38. doi: 10.1016/j.visres.2019.01.001. Epub 2019 Jan 23. Vision Res. 2019. PMID: 30633876 Free article.

5

Congenital orbital fibrosis: a distinct clinical entity.

Mavrikakis I, Pegado V, Lyons C, Rootman J. Mavrikakis I, et al. Orbit. 2009;28(1):43-9. doi: 10.1080/01676830802571795. Orbit. 2009. PMID: 19229745

6

Diffuse angiopathy in Adams-Oliver syndrome associated with truncating DOCK6 mutations.

Lehman A, Stittrich AB, Glusman G, Zong Z, Li H, Eydoux P, Senger C, Lyons C, Roach JC, Patel M. Lehman A, et al. Am J Med Genet A. 2014 Oct;164A(10):2656-62. doi: 10.1002/ajmg.a.36685. Epub 2014 Aug 4. Am J Med Genet A. 2014. PMID: 25091416 Free PMC article.

7

Deficient motion perception in the fellow eye of amblyopic children.

Ho CS, Giaschi DE, Boden C, Dougherty R, Cline R, Lyons C. Ho CS, et al. Vision Res. 2005 Jun;45(12):1615-27. doi: 10.1016/j.visres.2004.12.009. Vision Res. 2005. PMID: 15781077 Free article.

8

Psychophysical indexes of temporal processing abnormalities in children with developmental dyslexia.

Edwards VT, Giaschi DE, Dougherty RF, Edgell D, Bjornson BH, Lyons C, Douglas RM. Edwards VT, et al. Dev Neuropsychol. 2004;25(3):321-54. doi: 10.1207/s15326942dn2503_5. Dev Neuropsychol. 2004. PMID: 15148002

9

Conscious visual abilities in a patient with early bilateral occipital damage.

Giaschi D, Jan JE, Bjornson B, Young SA, Tata M, Lyons CJ, Good WV, Wong PK. Giaschi D, et al. Among authors: lyons cj. Dev Med Child Neurol. 2003 Nov;45(11):772-81. doi: 10.1111/j.1469-8749.2003.tb00888.x. Dev Med Child Neurol. 2003. PMID: 14580134 Free article.

10

Cerebrovasculopathy in NF1 associated with ocular and scalp defects.

Smith M, Heran MK, Connolly MB, Heran HK, Friedman JM, Jett K, Lyons CJ, Steinbok P, Armstrong L. Smith M, et al. Among authors: lyons cj. Am J Med Genet A. 2011 Feb;155A(2):380-5. doi: 10.1002/ajmg.a.33788. Epub 2010 Dec 22. Am J Med Genet A. 2011. PMID: 21271658

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