EY013583/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2002	2
2003	1
2004	2
2005	2
2006	5
2007	5
2008	1
2009	2
2010	5
2011	2
2012	1
2014	1
2025	0

1

The genetic basis of complex strabismus.

Engle EC. Engle EC. Pediatr Res. 2006 Mar;59(3):343-8. doi: 10.1203/01.pdr.0000200797.91630.08. Pediatr Res. 2006. PMID: 16492969 Review.

2

Human genetic disorders of axon guidance.

Engle EC. Engle EC. Cold Spring Harb Perspect Biol. 2010 Mar;2(3):a001784. doi: 10.1101/cshperspect.a001784. Cold Spring Harb Perspect Biol. 2010. PMID: 20300212 Free PMC article. Review.

3

Recent progress in understanding congenital cranial dysinnervation disorders.

Oystreck DT, Engle EC, Bosley TM. Oystreck DT, et al. J Neuroophthalmol. 2011 Mar;31(1):69-77. doi: 10.1097/WNO.0b013e31820d0756. J Neuroophthalmol. 2011. PMID: 21317732 Free PMC article. Review.

4

Expansion of the CHN1 strabismus phenotype.

Miyake N, Demer JL, Shaaban S, Andrews C, Chan WM, Christiansen SP, Hunter DG, Engle EC. Miyake N, et al. Invest Ophthalmol Vis Sci. 2011 Aug 11;52(9):6321-8. doi: 10.1167/iovs.11-7950. Invest Ophthalmol Vis Sci. 2011. PMID: 21715346 Free PMC article.

5

Distinct alpha- and beta-tubulin isotypes are required for the positioning, differentiation and survival of neurons: new support for the 'multi-tubulin' hypothesis.

Tischfield MA, Engle EC. Tischfield MA, et al. Biosci Rep. 2010 Apr 15;30(5):319-30. doi: 10.1042/BSR20100025. Biosci Rep. 2010. PMID: 20406197 Free PMC article. Review.

6

Evidence supporting extraocular muscle pulleys: refuting the platygean view of extraocular muscle mechanics.

Demer JL. Demer JL. J Pediatr Ophthalmol Strabismus. 2006 Sep-Oct;43(5):296-305. doi: 10.3928/01913913-20060901-05. J Pediatr Ophthalmol Strabismus. 2006. PMID: 17022164 Free PMC article. Review.

7

Human CFEOM1 mutations attenuate KIF21A autoinhibition and cause oculomotor axon stalling.

Cheng L, Desai J, Miranda CJ, Duncan JS, Qiu W, Nugent AA, Kolpak AL, Wu CC, Drokhlyansky E, Delisle MM, Chan WM, Wei Y, Propst F, Reck-Peterson SL, Fritzsch B, Engle EC. Cheng L, et al. Neuron. 2014 Apr 16;82(2):334-49. doi: 10.1016/j.neuron.2014.02.038. Epub 2014 Mar 20. Neuron. 2014. PMID: 24656932 Free PMC article.

8

A novel KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Marcus Gunn jaw-winking phenomenon.

Yamada K, Hunter DG, Andrews C, Engle EC. Yamada K, et al. Arch Ophthalmol. 2005 Sep;123(9):1254-9. doi: 10.1001/archopht.123.9.1254. Arch Ophthalmol. 2005. PMID: 16157808 Review.

9

KIF21A mutations in two Chinese families with congenital fibrosis of the extraocular muscles (CFEOM).

Yang X, Yamada K, Katz B, Guan H, Wang L, Andrews C, Zhao G, Engle EC, Chen H, Tong Z, Kong J, Hu C, Kong Q, Fan G, Wang Z, Ning M, Zhang S, Xu J, Zhang K. Yang X, et al. Mol Vis. 2010 Oct 13;16:2062-70. Mol Vis. 2010. PMID: 21042561 Free PMC article.

10

Magnetic resonance imaging of the endophenotype of a novel familial Möbius-like syndrome.

Dumars S, Andrews C, Chan WM, Engle EC, Demer JL. Dumars S, et al. J AAPOS. 2008 Aug;12(4):381-9. doi: 10.1016/j.jaapos.2008.01.018. Epub 2008 May 2. J AAPOS. 2008. PMID: 18455936 Free PMC article.

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