Khan AO - Search Results

1

Genomic analysis of pediatric cataract in Saudi Arabia reveals novel candidate disease genes.

Aldahmesh MA, Khan AO, Mohamed JY, Hijazi H, Al-Owain M, Alswaid A, Alkuraya FS. Aldahmesh MA, et al. Among authors: khan ao. Genet Med. 2012 Dec;14(12):955-62. doi: 10.1038/gim.2012.86. Epub 2012 Aug 30. Genet Med. 2012. PMID: 22935719 Free article.

2

A novel missense Norrie disease mutation associated with a severe ocular phenotype.

Khan AO, Shamsi FA, Al-Saif A, Kambouris M. Khan AO, et al. J Pediatr Ophthalmol Strabismus. 2004 Nov-Dec;41(6):361-3. doi: 10.3928/01913913-20041101-10. J Pediatr Ophthalmol Strabismus. 2004. PMID: 15609522

3

Recessive cornea plana in the Kingdom of Saudi Arabia.

Khan AO, Aldahmesh M, Meyer B. Khan AO, et al. Ophthalmology. 2006 Oct;113(10):1773-8. doi: 10.1016/j.ophtha.2006.04.026. Ophthalmology. 2006. PMID: 17011957

4

Familial blepharophimosis-like syndrome with esotropia, uveal coloboma, and short stature.

Khan AO, Alam SK, Aldahmesh M, Rajab M, Meyer B. Khan AO, et al. Ophthalmic Genet. 2006 Sep;27(3):79-82. doi: 10.1080/13816810600862501. Ophthalmic Genet. 2006. PMID: 17050282

5

Corneal ectasia and hydrops in a patient with autosomal recessive cornea plana.

Khan AO, Aldahmesh M, Meyer B. Khan AO, et al. Ophthalmic Genet. 2006 Sep;27(3):99-101. doi: 10.1080/13816810600862469. Ophthalmic Genet. 2006. PMID: 17050286

6

The enhanced S-cone syndrome in children.

Khan AO, Aldahmesh M, Meyer B. Khan AO, et al. Br J Ophthalmol. 2007 Mar;91(3):394-6. doi: 10.1136/bjo.2006.097956. Br J Ophthalmol. 2007. PMID: 17322467 Free PMC article. No abstract available.

7

Recessive congenital total cataract with microcornea and heterozygote carrier signs caused by a novel missense CRYAA mutation (R54C).

Khan AO, Aldahmesh MA, Meyer B. Khan AO, et al. Am J Ophthalmol. 2007 Dec;144(6):949-952. doi: 10.1016/j.ajo.2007.08.005. Epub 2007 Oct 15. Am J Ophthalmol. 2007. PMID: 17937925

8

Correlation of ophthalmic examination with carrier status in females potentially harboring a severe Norrie disease gene mutation.

Khan AO, Aldahmesh MA, Meyer B. Khan AO, et al. Ophthalmology. 2008 Apr;115(4):730-3. doi: 10.1016/j.ophtha.2007.04.064. Ophthalmology. 2008. PMID: 18387409

9

PAX6 analysis of two unrelated families from the Arabian Peninsula with classic hereditary aniridia.

Khan AO, Aldahmesh MA. Khan AO, et al. Ophthalmic Genet. 2008 Sep;29(3):145-8. doi: 10.1080/13816810802078195. Ophthalmic Genet. 2008. PMID: 18766996

10

Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative example.

Aldahmesh MA, Abu-Safieh L, Khan AO, Al-Hassnan ZN, Shaheen R, Rajab M, Monies D, Meyer BF, Alkuraya FS. Aldahmesh MA, et al. Among authors: khan ao. Am J Med Genet A. 2009 Feb 15;149A(4):662-5. doi: 10.1002/ajmg.a.32753. Am J Med Genet A. 2009. PMID: 19283855

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