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Results: 7

1.

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.

Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2218-23.

PMID:
15223798
[PubMed - indexed for MEDLINE]
Free Article
2.

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.

Arch Ophthalmol. 2005 Sep;123(9):1254-9. Review.

PMID:
16157808
[PubMed - indexed for MEDLINE]
3.

Congenital fibrosis of the extraocular muscles.

Heidary G, Engle EC, Hunter DG.

Semin Ophthalmol. 2008 Jan-Feb;23(1):3-8. doi: 10.1080/08820530701745181. Review.

PMID:
18214786
[PubMed - indexed for MEDLINE]
4.

[Congenital fibrosis of extraocular muscles (CFEOM) and other phenotypes of congenital cranial dysinnervation syndromes (CCDD)].

Hanisch F, Bau V, Zierz S.

Nervenarzt. 2005 Apr;76(4):395-402. Review. German.

PMID:
15221064
[PubMed - indexed for MEDLINE]
5.

Applications of molecular genetics to the understanding of congenital ocular motility disorders.

Engle EC.

Ann N Y Acad Sci. 2002 Apr;956:55-63. Review.

PMID:
11960793
[PubMed - indexed for MEDLINE]
6.

The genetic basis of complex strabismus.

Engle EC.

Pediatr Res. 2006 Mar;59(3):343-8. Review.

PMID:
16492969
[PubMed - indexed for MEDLINE]
7.

[Ophthalmoplegia].

Numabe H.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):378-9. Review. Japanese. No abstract available.

PMID:
11528793
[PubMed - indexed for MEDLINE]

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