EY12498/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2000	1
2001	1
2002	2
2003	2
2004	2
2006	2
2007	1
2010	2
2011	1
2013	1
2024	0

1

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.

2

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.

3

The genetic basis of incomitant strabismus: consolidation of the current knowledge of the genetic foundations of disease.

Graeber CP, Hunter DG, Engle EC. Graeber CP, et al. Semin Ophthalmol. 2013 Sep-Nov;28(5-6):427-37. doi: 10.3109/08820538.2013.825288. Semin Ophthalmol. 2013. PMID: 24138051 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

Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A.

Bosley TM, Oystreck DT, Robertson RL, al Awad A, Abu-Amero K, Engle EC. Bosley TM, et al. Brain. 2006 Sep;129(Pt 9):2363-74. doi: 10.1093/brain/awl161. Epub 2006 Jun 30. Brain. 2006. PMID: 16815872

6

Congenital fibrosis syndrome associated with central nervous system abnormalities.

Pieh C, Goebel HH, Engle EC, Gottlob I. Pieh C, et al. Graefes Arch Clin Exp Ophthalmol. 2003 Jul;241(7):546-553. doi: 10.1007/s00417-003-0703-z. Epub 2003 Jun 18. Graefes Arch Clin Exp Ophthalmol. 2003. PMID: 12819981

7

A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).

Yazdani A, Chung DC, Abbaszadegan MR, Al-Khayer K, Chan WM, Yazdani M, Ghodsi K, Engle EC, Traboulsi EI. Yazdani A, et al. Am J Ophthalmol. 2003 Nov;136(5):861-5. doi: 10.1016/s0002-9394(03)00891-2. Am J Ophthalmol. 2003. PMID: 14597037

8

Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).

Yamada K, Chan WM, Andrews C, Bosley TM, Sener EC, Zwaan JT, Mullaney PB, Oztürk BT, Akarsu AN, Sabol LJ, Demer JL, Sullivan TJ, Gottlob I, Roggenkäemper P, Mackey DA, De Uzcategui CE, Uzcategui N, Ben-Zeev B, Traboulsi EI, Magli A, de Berardinis T, Gagliardi V, Awasthi-Patney S, Vogel MC, Rizzo JF 3rd, Engle EC. Yamada K, et al. Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2218-23. doi: 10.1167/iovs.03-1413. Invest Ophthalmol Vis Sci. 2004. PMID: 15223798

9

Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.

Nakano M, Yamada K, Fain J, Sener EC, Selleck CJ, Awad AH, Zwaan J, Mullaney PB, Bosley TM, Engle EC. Nakano M, et al. Nat Genet. 2001 Nov;29(3):315-20. doi: 10.1038/ng744. Nat Genet. 2001. PMID: 11600883

10

The molecular basis of the congenital fibrosis syndromes.

Engle EC. Engle EC. Strabismus. 2002 Jun;10(2):125-8. doi: 10.1076/stra.10.2.125.8142. Strabismus. 2002. PMID: 12221491

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