Khan AO - Search Results

1

Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia.

Aldahmesh MA, Khan AO, Meyer BF, Alkuraya FS. Aldahmesh MA, et al. Among authors: khan ao. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4142-5. doi: 10.1167/iovs.08-3006. Epub 2009 Apr 15. Invest Ophthalmol Vis Sci. 2009. PMID: 19369245

2

A novel KERA mutation associated with autosomal recessive cornea plana.

Khan A, Al-Saif A, Kambouris M. Khan A, et al. Ophthalmic Genet. 2004 Jun;25(2):147-52. doi: 10.1080/13816810490514397. Ophthalmic Genet. 2004. PMID: 15370545

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

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. Ophthalmology. 2008 Dec;115(12):2262-5. doi: 10.1016/j.ophtha.2008.08.010. Ophthalmology. 2008. PMID: 19041479

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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