Pal B - Search Results

1

Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism.

Poulter JA, Al-Araimi M, Conte I, van Genderen MM, Sheridan E, Carr IM, Parry DA, Shires M, Carrella S, Bradbury J, Khan K, Lakeman P, Sergouniotis PI, Webster AR, Moore AT, Pal B, Mohamed MD, Venkataramana A, Ramprasad V, Shetty R, Saktivel M, Kumaramanickavel G, Tan A, Mackey DA, Hewitt AW, Banfi S, Ali M, Inglehearn CF, Toomes C. Poulter JA, et al. Among authors: pal b. Am J Hum Genet. 2013 Dec 5;93(6):1143-50. doi: 10.1016/j.ajhg.2013.11.002. Epub 2013 Nov 27. Am J Hum Genet. 2013. PMID: 24290379 Free PMC article. Review.

2

A new recessively inherited disorder composed of foveal hypoplasia, optic nerve decussation defects and anterior segment dysgenesis maps to chromosome 16q23.3-24.1.

Al-Araimi M, Pal B, Poulter JA, van Genderen MM, Carr I, Cudrnak T, Brown L, Sheridan E, Mohamed MD, Bradbury J, Ali M, Inglehearn CF, Toomes C. Al-Araimi M, et al. Among authors: pal b. Mol Vis. 2013 Nov 1;19:2165-72. eCollection 2013. Mol Vis. 2013. PMID: 24194637 Free PMC article.

3

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. Pal B, et al. J Med Genet. 2004 Oct;41(10):772-7. doi: 10.1136/jmg.2004.020040. J Med Genet. 2004. PMID: 15466012 Free PMC article. No abstract available.

4

Genotype-phenotype correlation for leber congenital amaurosis in Northern Pakistan.

McKibbin M, Ali M, Mohamed MD, Booth AP, Bishop F, Pal B, Springell K, Raashid Y, Jafri H, Inglehearn CF. McKibbin M, et al. Among authors: pal b. Arch Ophthalmol. 2010 Jan;128(1):107-13. doi: 10.1001/archophthalmol.2010.309. Arch Ophthalmol. 2010. PMID: 20065226

5

Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2.

Subash M, Rotsos T, Wright GA, Devery S, Holder GE, Robson AG, Pal B, Tufail A, Webster AR, Moore AT, Michaelides M. Subash M, et al. Among authors: pal b. Br J Ophthalmol. 2012 May;96(5):719-22. doi: 10.1136/bjophthalmol-2011-300964. Epub 2011 Dec 15. Br J Ophthalmol. 2012. PMID: 22174098

6

Unilateral pigmentary retinopathy: a retrospective case series.

Errera MH, Robson AG, Wong T, Hykin PG, Pal B, Sagoo MS, Pavesio CE, Moore AT, Webster AR, MacLaren RE, Holder GE. Errera MH, et al. Among authors: pal b. Acta Ophthalmol. 2019 Jun;97(4):e601-e617. doi: 10.1111/aos.13981. Epub 2018 Dec 31. Acta Ophthalmol. 2019. PMID: 30597758 Free article.

7

Responsiveness of choroidal neovascular membranes in patients with R345W mutation in fibulin 3 (Doyne honeycomb retinal dystrophy) to anti-vascular endothelial growth factor therapy.

Sohn EH, Patel PJ, MacLaren RE, Adatia FA, Pal B, Webster AR, Tufail A. Sohn EH, et al. Among authors: pal b. Arch Ophthalmol. 2011 Dec;129(12):1626-8. doi: 10.1001/archophthalmol.2011.338. Arch Ophthalmol. 2011. PMID: 22159686 No abstract available.

8

Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy.

Graham PS, Kaidonis G, Abhary S, Gillies MC, Daniell M, Essex RW, Chang JH, Lake SR, Pal B, Jenkins AJ, Hewitt AW, Lamoureux EL, Hykin PG, Petrovsky N, Brown MA, Craig JE, Burdon KP. Graham PS, et al. Among authors: pal b. BMC Med Genet. 2018 May 8;19(1):71. doi: 10.1186/s12881-018-0587-8. BMC Med Genet. 2018. PMID: 29739359 Free PMC article.

9

Phenotypic progression in X-linked retinitis pigmentosa secondary to a novel mutation in the RPGR gene.

Al-Maskari A, O'grady A, Pal B, McKibbin M. Al-Maskari A, et al. Among authors: pal b. Eye (Lond). 2009 Mar;23(3):519-21. doi: 10.1038/eye.2008.427. Epub 2009 Feb 13. Eye (Lond). 2009. PMID: 19218993

10

Genetic study of diabetic retinopathy: recruitment methodology and analysis of baseline characteristics.

Kaidonis G, Abhary S, Daniell M, Gillies M, Fogarty R, Petrovsky N, Jenkins A, Essex R, Chang JH, Pal B, Hewitt AW, Burdon KP, Craig JE. Kaidonis G, et al. Among authors: pal b. Clin Exp Ophthalmol. 2014 Jul;42(5):486-93. doi: 10.1111/ceo.12239. Epub 2013 Oct 28. Clin Exp Ophthalmol. 2014. PMID: 24112246

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