Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 55

1.

The association between petrous apex cephalocele and empty sella.

Jamjoom DZ, Alorainy IA.

Surg Radiol Anat. 2015 May 12. [Epub ahead of print]

PMID:
25963119
2.

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
3.

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. No abstract available.

PMID:
24878468
4.

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
5.

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
6.

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
7.

Preimplantation genetic diagnosis in isolated sulfite oxidase deficiency.

Salih MA, Bosley TM, Alorainy IA, Sabry MA, Rashed MS, Al-Yamani EA, El-Akoum S, Mohamed SH, Abu-Amero KK, Hellani AM.

Can J Neurol Sci. 2013 Jan;40(1):109-12. No abstract available.

PMID:
23250141
8.

A novel syndrome of lethal familial hyperekplexia associated with brain malformation.

Seidahmed MZ, Salih MA, Abdulbasit OB, Shaheed M, Al Hussein K, Miqdad AM, Al Rasheed AK, Alazami AM, Alorainy IA, Alkuraya FS.

BMC Neurol. 2012 Oct 27;12:125. doi: 10.1186/1471-2377-12-125.

9.

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.

Ophthalmic Genet. 2013 Mar-Jun;34(1-2):90-6. doi: 10.3109/13816810.2012.718850. Epub 2012 Sep 6.

PMID:
22950449
10.

Visual loss in orbitofacial neurofibromatosis type 1.

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

Ophthalmology. 2012 Oct;119(10):2168-73. doi: 10.1016/j.ophtha.2012.04.032. Epub 2012 Jun 17.

PMID:
22709421
11.

The neurology of carbonic anhydrase type II deficiency syndrome.

Bosley TM, Salih MA, Alorainy IA, Islam MZ, Oystreck DT, Suliman OS, al Malki S, Suhaibani AH, Khiari H, Beckers S, van Wesenbeeck L, Perdu B, AlDrees A, Elmalik SA, Van Hul W, Abu-Amero KK.

Brain. 2011 Dec;134(Pt 12):3502-15. doi: 10.1093/brain/awr302. Epub 2011 Nov 26.

12.

Horizontal gaze palsy and progressive scoliosis without ROBO3 mutations.

Abu-Amero KK, Faletra F, Gasparini P, Parentin F, Pensiero S, Alorainy IA, Hellani AM, Catalano D, Bosley TM.

Ophthalmic Genet. 2011 Nov;32(4):212-6. doi: 10.3109/13816810.2011.574186. Epub 2011 Apr 21.

PMID:
21510772
13.

A practical discussion to avoid common pitfalls when constructing multiple choice questions items.

Al-Faris EA, Alorainy IA, Abdel-Hameed AA, Al-Rukban MO.

J Family Community Med. 2010 May;17(2):96-102. doi: 10.4103/1319-1683.71992.

14.

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis.

Salih MA, Abu-Amero KK, Alrasheed S, Alorainy IA, Liu L, McGrath JA, Van Maldergem L, Al-Faky YH, AlSuhaibani AH, Oystreck DT, Bosley TM.

BMC Med Genet. 2011 Feb 24;12:31. doi: 10.1186/1471-2350-12-31.

15.

Pictorial Essay: Infants of diabetic mothers.

Alorainy IA, Barlas NB, Al-Boukai AA.

Indian J Radiol Imaging. 2010 Aug;20(3):174-81. doi: 10.4103/0971-3026.69349.

16.

Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy.

Abu-Amero KK, Hellani A, Salih MA, Alorainy IA, Zidan G, Kern KC, Sicotte NL, Bosley TM.

Ophthalmic Genet. 2010 Sep;31(3):147-54. doi: 10.3109/13816810.2010.492817.

PMID:
20565246
17.

Ophthalmologic abnormalities in a de novo terminal 6q deletion.

Abu-Amero KK, Hellani A, Salih MA, Al Hussain A, al Obailan M, Zidan G, Alorainy IA, Bosley TM.

Ophthalmic Genet. 2010 Mar;31(1):1-11. doi: 10.3109/13816810903312535.

PMID:
20141352
18.

Ophthalmic features of Joubert syndrome.

Khan AO, Oystreck DT, Seidahmed MZ, AlDrees A, Elmalik SA, Alorainy IA, Salih MA.

Ophthalmology. 2008 Dec;115(12):2286-9. doi: 10.1016/j.ophtha.2008.08.005.

PMID:
19041481
19.

A 45-year old man with headache, double vision, and facial numbness.

Alkali NH, Tahan AY, Al-Rikabi AC, Alorainy IA, Al-Balla SM.

Neurosciences (Riyadh). 2008 Jul;13(3):328; quiz 329. No abstract available.

PMID:
21063356
20.

The clinical spectrum of homozygous HOXA1 mutations.

Bosley TM, Alorainy IA, Salih MA, Aldhalaan HM, Abu-Amero KK, Oystreck DT, Tischfield MA, Engle EC, Erickson RP.

Am J Med Genet A. 2008 May 15;146A(10):1235-40. doi: 10.1002/ajmg.a.32262.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk