Meyer BF - 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: meyer bf. 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 form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14.

Hodgkinson CA, Bohlega S, Abu-Amero SN, Cupler E, Kambouris M, Meyer BF, Bharucha VA. Hodgkinson CA, et al. Among authors: meyer bf. Neurology. 2002 Dec 24;59(12):1905-9. doi: 10.1212/01.wnl.0000036909.49629.21. Neurology. 2002. PMID: 12499481

3

Pellucid marginal degeneration coexistent with cornea plana in one member of a family exhibiting a novel KERA mutation.

Khan AO, Aldahmesh M, Al-Saif A, Meyer B. Khan AO, et al. Br J Ophthalmol. 2005 Nov;89(11):1538-40. doi: 10.1136/bjo.2005.073510. Br J Ophthalmol. 2005. PMID: 16234475 Free PMC article. No abstract available.

4

Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria.

Al-Sayed M, Alahmed S, Alsmadi O, Khalil H, Rashed MS, Imtiaz F, Meyer BF. Al-Sayed M, et al. Among authors: meyer bf. J Inherit Metab Dis. 2005;28(6):877-83. doi: 10.1007/s10545-005-0081-2. J Inherit Metab Dis. 2005. PMID: 16435180

5

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

6

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

7

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

8

Mutations underlying 3-hydroxy-3-methylglutaryl CoA lyase deficiency in the Saudi population.

Al-Sayed M, Imtiaz F, Alsmadi OA, Rashed MS, Meyer BF. Al-Sayed M, et al. Among authors: meyer bf. BMC Med Genet. 2006 Dec 16;7:86. doi: 10.1186/1471-2350-7-86. BMC Med Genet. 2006. PMID: 17173698 Free PMC article.

9

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.

10

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

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