PubMed

Further insight into West African crystalline maculopathy.

Rajak SN, Mohamed MD, Pelosini L.

Arch Ophthalmol. 2009 Jul;127(7):863-8.PMID: 19597105 [PubMed - indexed for MEDLINE]Related articles

A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration.

Ali M, Ramprasad VL, Soumittra N, Mohamed MD, Jafri H, Rashid Y, Danciger M, McKibbin M, Kumaramanickavel G, Inglehearn CF.

Mol Vis. 2008;14:1960-4. Epub 2008 Oct 30.PMID: 18978954 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.

den Hollander AI, Koenekoop RK, Mohamed MD, Arts HH, Boldt K, Towns KV, Sedmak T, Beer M, Nagel-Wolfrum K, McKibbin M, Dharmaraj S, Lopez I, Ivings L, Williams GA, Springell K, Woods CG, Jafri H, Rashid Y, Strom TM, van der Zwaag B, Gosens I, Kersten FF, van Wijk E, Veltman JA, Zonneveld MN, van Beersum SE, Maumenee IH, Wolfrum U, Cheetham ME, Ueffing M, Cremers FP, Inglehearn CF, Roepman R.

Nat Genet. 2007 Jul;39(7):889-95. Epub 2007 Jun 3.PMID: 17546029 [PubMed - indexed for MEDLINE]Related articles

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).

Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T.

Nat Genet. 2006 Jul;38(7):755-7. Epub 2006 Jun 11.PMID: 16767101 [PubMed - indexed for MEDLINE]Related articles

Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.

Woods CG, Cox J, Springell K, Hampshire DJ, Mohamed MD, McKibbin M, Stern R, Raymond FL, Sandford R, Malik Sharif S, Karbani G, Ahmed M, Bond J, Clayton D, Inglehearn CF.

Am J Hum Genet. 2006 May;78(5):889-96. Epub 2006 Mar 21.PMID: 16642444 [PubMed - indexed for MEDLINE]Related articlesFree article

Ultrasound biomicroscopy in the management of melanocytoma of the ciliary body with extrascleral extension.

Mohamed MD, Gupta M, Parsons A, Rennie IG.

Br J Ophthalmol. 2005 Jan;89(1):14-6.PMID: 15615738 [PubMed - indexed for MEDLINE]Related articlesFree article

A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2-24.2.

Pal B, Mohamed MD, Keen TJ, Williams GA, Bradbury JA, Sheridan E, Inglehearn CF.

J Med Genet. 2004 Oct;41(10):772-7. No abstract available. PMID: 15466012 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic, ophthalmic, morphometric and histopathological analysis of the Retinopathy Globe Enlarged (rge) chicken.

Inglehearn CF, Morrice DR, Lester DH, Robertson GW, Mohamed MD, Simmons I, Downey LM, Thaung C, Bridges LR, Paton IR, Smith J, Petersen-Jones S, Hocking PM, Burt DW.

Mol Vis. 2003 Jul 1;9:295-300.PMID: 12847422 [PubMed - indexed for MEDLINE]Related articlesFree article

Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36.

Keen TJ, Mohamed MD, McKibbin M, Rashid Y, Jafri H, Maumenee IH, Inglehearn CF.

Eur J Hum Genet. 2003 May;11(5):420-3.PMID: 12734549 [PubMed - indexed for MEDLINE]Related articlesFree article

Analysis of the rdd locus in chicken: a model for human retinitis pigmentosa.

Burt DW, Morrice DR, Lester DH, Robertson GW, Mohamed MD, Simmons I, Downey LM, Thaung C, Bridges LR, Paton IR, Gentle M, Smith J, Hocking PM, Inglehearn CF.

Mol Vis. 2003 Apr 30;9:164-70.PMID: 12724645 [PubMed - indexed for MEDLINE]Related articlesFree article

Further considerations of retinopathy with renal failure.

Mohamed MD, McKibbin MA.

Br J Ophthalmol. 2003 May;87(5):659. No abstract available. PMID: 12714427 [PubMed - indexed for MEDLINE]Related articlesFree article

Progression of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus.

Mohamed MD, Topping NC, Jafri H, Raashed Y, McKibbin MA, Inglehearn CF.

Br J Ophthalmol. 2003 Apr;87(4):473-5.PMID: 12642313 [PubMed - indexed for MEDLINE]Related articlesFree article

A new pedigree with recessive mapping to CHED2 locus on 20p13.

Mohamed MD, McKibbin M, Jafri H, Rasheed Y, Woods CG, Inglehearn CF.

Br J Ophthalmol. 2001 Jun;85(6):758-9. No abstract available. PMID: 11439918 [PubMed - indexed for MEDLINE]Related articlesFree article

Unidirectional dyslexia in a polyglot.

Mohamed MD, Elsherbiny SM, Goulding PJ.

J Neurol Neurosurg Psychiatry. 2000 Apr;68(4):537. No abstract available. PMID: 10847799 [PubMed - indexed for MEDLINE]Related articlesFree article