Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 42

1.

NEW OBSERVATIONS REGARDING THE RETINOPATHY OF GENETICALLY CONFIRMED KEARNS-SAYRE SYNDROME.

Kozak I, Oystreck DT, Abu-Amero KK, Nowilaty SR, Alkhalidi H, Elkhamary SM, Mohamed S, Hamad MH, Salih MA, Blakely EL, Taylor RW, Bosley TM.

Retin Cases Brief Rep. 2016 Dec 19. doi: 10.1097/ICB.0000000000000503. [Epub ahead of print]

PMID:
28296806
2.

The genetics of nonsyndromic bilateral Duane retraction syndrome.

Abu-Amero KK, Khan AO, Oystreck DT, Kondkar AA, Bosley TM.

J AAPOS. 2016 Oct;20(5):396-400.e2. doi: 10.1016/j.jaapos.2016.06.008. Epub 2016 Sep 20.

PMID:
27658539
3.

Duane Retraction Syndrome Associated with a Small X Chromosome Deletion.

Abu-Amero KK, Kondkar AA, Odan HA, Khan AO, Oystreck DT, Bosley TM.

Can J Neurol Sci. 2016 May;43(3):445-7. doi: 10.1017/cjn.2015.358. Epub 2016 Jan 25. No abstract available.

PMID:
26891113
4.

Duane retraction syndrome in a patient with Duchenne muscular dystrophy.

Bosley TM, Salih MA, Alkhalidi H, Oystreck DT, El Khashab HY, Kondkar AA, Abu-Amero KK.

Ophthalmic Genet. 2016 Sep;37(3):276-80. doi: 10.3109/13816810.2015.1039139. Epub 2016 Feb 5.

PMID:
26849454
5.

Ocular motility abnormalities in orbitofacial neurofibromatosis type 1.

Oystreck DT, Alorainy IA, Morales J, Chaudhry IA, Elkhamary SM, Bosley TM.

J AAPOS. 2014 Aug;18(4):338-43. doi: 10.1016/j.jaapos.2014.02.018.

PMID:
25173895
6.

Retinal Dysfunction in Patients with Congenital Fibrosis of the Extraocular Muscles Type 2.

Khan AO, Almutlaq M, Oystreck DT, Engle EC, Abu-Amero K, Bosley T.

Ophthalmic Genet. 2016 Jun;37(2):130-6. doi: 10.3109/13816810.2014.926942. Epub 2014 Jun 18.

7.

HOXA1 Mutations are Not Commonly Associated with Non-Syndromic Deafness.

Abu-Amero KK, Hagr Aa, Almomani MO, Azad TA, Alorainy IA, Oystreck DT, Bosley TM.

Can J Neurol Sci. 2014 Jul;41(4):448-51.

PMID:
24878468
8.

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

Abu-Amero KK, Kondkar AA, Oystreck DT, Khan AO, Bosley TM.

Ophthalmic Genet. 2014 Sep;35(3):162-9. doi: 10.3109/13816810.2014.921317. Epub 2014 May 27.

PMID:
24865192
9.

Diagnostic distinctions and genetic analysis of patients diagnosed with moebius syndrome.

MacKinnon S, Oystreck DT, Andrews C, Chan WM, Hunter DG, Engle EC.

Ophthalmology. 2014 Jul;121(7):1461-8. doi: 10.1016/j.ophtha.2014.01.006. Epub 2014 Mar 6.

10.

CCDD Phenotype Associated with a Small Chromosome 2 Deletion.

Abu-Amero KK, Bosley TM, Kondkar AA, Oystreck DT, Khan AO.

Semin Ophthalmol. 2015;30(5-6):435-42. doi: 10.3109/08820538.2013.874474. Epub 2014 Jan 29.

PMID:
24475916
11.

Neurologic injury in isolated sulfite oxidase deficiency.

Bosley TM, Alorainy IA, Oystreck DT, Hellani AM, Seidahmed MZ, Osman Mel F, Sabry MA, Rashed MS, Al-Yamani EA, Abu-Amero KK, Salih MA.

Can J Neurol Sci. 2014 Jan;41(1):42-8.

PMID:
24384336
12.

Nicotinic Receptor Mutation in a Mildly Dysmorphic Girl with Duane Retraction Syndrome.

Abu-Amero KK, Kondkar A, Hellani AM, Oystreck DT, Khan AO, Bosley TM.

Ophthalmic Genet. 2015 Jun;36(2):99-104. doi: 10.3109/13816810.2013.835431. Epub 2013 Sep 3.

PMID:
24001015
13.

Comitant strabismus: Perspectives, present and future.

Oystreck DT, Lyons CJ.

Saudi J Ophthalmol. 2012 Jul;26(3):265-70. doi: 10.1016/j.sjopt.2012.05.002. Epub 2012 May 23.

14.

Partial duplication of chromosome 19 associated with syndromic duane retraction syndrome.

Abu-Amero KK, Kondkar AA, Al Otaibi A, Alorainy IA, Khan AO, Hellani AM, Oystreck DT, Bosley TM.

Ophthalmic Genet. 2015 Mar;36(1):14-20. doi: 10.3109/13816810.2013.827218. Epub 2013 Aug 19.

PMID:
23952617
15.

Congenital cranial dysinnervation disorders: a concept in evolution.

Bosley TM, Abu-Amero KK, Oystreck DT.

Curr Opin Ophthalmol. 2013 Sep;24(5):398-406. doi: 10.1097/ICU.0b013e3283645ad6. Review.

PMID:
23872818
16.

Variable ptosis after botulinum toxin type a injection with positive ice test mimicking ocular myasthenia gravis.

Alaraj AM, Oystreck DT, Bosley TM.

J Neuroophthalmol. 2013 Jun;33(2):169-71. doi: 10.1097/WNO.0b013e31828bb19b.

PMID:
23681240
17.

A newly recognized autosomal recessive syndrome affecting neurologic function and vision.

Salih MA, Tzschach A, Oystreck DT, Hassan HH, AlDrees A, Elmalik SA, El Khashab HY, Wienker TF, Abu-Amero KK, Bosley TM.

Am J Med Genet A. 2013 Jun;161A(6):1207-13. doi: 10.1002/ajmg.a.35850. Epub 2013 Apr 30.

PMID:
23633300
18.

Ophthalmologic observations in a patient with partial mosaic trisomy 8.

Abu-Amero KK, Kondkar AA, Salih MA, Al-Husain M, Al Shammari M, Zeidan G, Oystreck DT, Hellani AM, Kentab AY, Bosley TM.

Ophthalmic Genet. 2013 Dec;34(4):249-53. doi: 10.3109/13816810.2012.762933. Epub 2013 Feb 13.

PMID:
23406309
19.

A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3.

Chew S, Balasubramanian R, Chan WM, Kang PB, Andrews C, Webb BD, MacKinnon SE, Oystreck DT, Rankin J, Crawford TO, Geraghty M, Pomeroy SL, Crowley WF Jr, Jabs EW, Hunter DG, Grant PE, Engle EC.

Brain. 2013 Feb;136(Pt 2):522-35. doi: 10.1093/brain/aws345. Epub 2013 Jan 31.

20.

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.

Ophthalmic Genet. 2014 Mar;35(1):18-24. doi: 10.3109/13816810.2013.766218. Epub 2013 Feb 1.

PMID:
23373430

Supplemental Content

Loading ...
Support Center