Oystreck DT - Search Results

1

Congenital cranial dysinnervation disorders: a concept in evolution.

Bosley TM, Abu-Amero KK, Oystreck DT. Bosley TM, et al. Among authors: oystreck dt. Curr Opin Ophthalmol. 2013 Sep;24(5):398-406. doi: 10.1097/ICU.0b013e3283645ad6. Curr Opin Ophthalmol. 2013. PMID: 23872818 Review.

2

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. Among authors: oystreck dt. Brain. 2006 Sep;129(Pt 9):2363-74. doi: 10.1093/brain/awl161. Epub 2006 Jun 30. Brain. 2006. PMID: 16815872

3

Bilateral synergistic convergence associated with homozygous ROB03 mutation (p.Pro771Leu).

Khan AO, Oystreck DT, Al-Tassan N, Al-Sharif L, Bosley TM. Khan AO, et al. Among authors: oystreck dt. Ophthalmology. 2008 Dec;115(12):2262-5. doi: 10.1016/j.ophtha.2008.08.010. Ophthalmology. 2008. PMID: 19041479

4

Synergistic divergence: a distinct ocular motility dysinnervation pattern.

Oystreck DT, Khan AO, Vila-Coro AA, Oworu O, Al-Tassan N, Chan WM, Engle EC, Bosley TM. Oystreck DT, et al. Invest Ophthalmol Vis Sci. 2009 Nov;50(11):5213-6. doi: 10.1167/iovs.08-2928. Epub 2009 Jul 2. Invest Ophthalmol Vis Sci. 2009. PMID: 19578026 Free PMC article.

5

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.

6

When straight eyes won't move: phenotypic overlap of genetically distinct ocular motility disturbances.

Oystreck DT, Salih MA, Bosley TM. Oystreck DT, et al. Can J Ophthalmol. 2011 Dec;46(6):477-80. doi: 10.1016/j.jcjo.2011.09.009. Can J Ophthalmol. 2011. PMID: 22153632

7

Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder.

Abu-Amero KK, Kondkar AA, Salih MA, Alorainy IA, Khan AO, Oystreck DT, Bosley TM. Abu-Amero KK, et al. Among authors: oystreck dt. Ophthalmic Genet. 2013 Mar-Jun;34(1-2):90-6. doi: 10.3109/13816810.2012.718850. Epub 2012 Sep 6. Ophthalmic Genet. 2013. PMID: 22950449

8

Xq26.3 microdeletion in a male with Wildervanck Syndrome.

Abu-Amero KK, Kondkar AA, Alorainy IA, Khan AO, Al-Enazy LA, Oystreck DT, Bosley TM. Abu-Amero KK, et al. Among authors: oystreck dt. Ophthalmic Genet. 2014 Mar;35(1):18-24. doi: 10.3109/13816810.2013.766218. Epub 2013 Feb 1. Ophthalmic Genet. 2014. PMID: 23373430

9

CCDD Phenotype Associated with a Small Chromosome 2 Deletion.

Abu-Amero KK, Bosley TM, Kondkar AA, Oystreck DT, Khan AO. Abu-Amero KK, et al. Among authors: oystreck dt. Semin Ophthalmol. 2015;30(5-6):435-42. doi: 10.3109/08820538.2013.874474. Epub 2014 Jan 29. Semin Ophthalmol. 2015. PMID: 24475916

10

Microdeletions involving chromosomes 12 and 22 associated with syndromic Duane retraction syndrome.

Abu-Amero KK, Kondkar AA, Oystreck DT, Khan AO, Bosley TM. Abu-Amero KK, et al. Among authors: oystreck dt. Ophthalmic Genet. 2014 Sep;35(3):162-9. doi: 10.3109/13816810.2014.921317. Epub 2014 May 27. Ophthalmic Genet. 2014. PMID: 24865192

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