Hodgkins PR - Search Results

1

Association of HLA class I and class II polymorphisms with age-related macular degeneration.

Goverdhan SV, Howell MW, Mullins RF, Osmond C, Hodgkins PR, Self J, Avery K, Lotery AJ. Goverdhan SV, et al. Among authors: hodgkins pr. Invest Ophthalmol Vis Sci. 2005 May;46(5):1726-34. doi: 10.1167/iovs.04-0928. Invest Ophthalmol Vis Sci. 2005. PMID: 15851575

2

Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus.

Self JE, Shawkat F, Malpas CT, Thomas NS, Harris CM, Hodgkins PR, Chen X, Trump D, Lotery AJ. Self JE, et al. Among authors: hodgkins pr. Arch Ophthalmol. 2007 Sep;125(9):1255-63. doi: 10.1001/archopht.125.9.1255. Arch Ophthalmol. 2007. PMID: 17846367

3

Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3.

Self JE, Ennis S, Collins A, Shawkat F, Harris CM, Mackey DA, Hodgkins PR, Temple IK, Chen X, Lotery AJ. Self JE, et al. Among authors: hodgkins pr. Mol Vis. 2006 Oct 18;12:1211-6. Mol Vis. 2006. PMID: 17102799 Free article.

4

Infantile nystagmus and late onset ataxia associated with a CACNA1A mutation in the intracellular loop between s4 and s5 of domain 3.

Self J, Mercer C, Boon EM, Murugavel M, Shawkat F, Hammans S, Hodgkins P, Griffiths H, Lotery A. Self J, et al. Eye (Lond). 2009 Dec;23(12):2251-5. doi: 10.1038/eye.2008.389. Eye (Lond). 2009. PMID: 19182766

5

Incidence and patterns of detection and management of childhood-onset hereditary retinal disorders in the UK.

Hamblion EL, Moore AT, Rahi JS; British Childhood Onset Hereditary Retinal Disorders Network. Hamblion EL, et al. Br J Ophthalmol. 2012 Mar;96(3):360-5. doi: 10.1136/bjo.2010.201178. Epub 2011 Jun 7. Br J Ophthalmol. 2012. PMID: 21653210

6

Bilateral retinoblastoma presenting at retinopathy of prematurity screening.

Self J, Bush K, Baral VR, Puvanachandra N, Puddy VF, Hodgkins P. Self J, et al. Arch Dis Child Fetal Neonatal Ed. 2010 Jul;95(4):F292. doi: 10.1136/adc.2009.178780. Arch Dis Child Fetal Neonatal Ed. 2010. PMID: 20576664 No abstract available.

7

Immunophenotyping in presumed ocular histoplasmosis like retinopathy.

Hodgkins PR, Lane AC, Chisholm IH, Absolon MJ, Elkington AR, Smith JL. Hodgkins PR, et al. Eye (Lond). 1995;9 ( Pt 1):56-63. doi: 10.1038/eye.1995.8. Eye (Lond). 1995. PMID: 7713251

8

Current practice of cataract extraction and anaesthesia.

Hodgkins PR, Luff AJ, Morrell AJ, Botchway LT, Featherston TJ, Fielder AR. Hodgkins PR, et al. Br J Ophthalmol. 1992 Jun;76(6):323-6. doi: 10.1136/bjo.76.6.323. Br J Ophthalmol. 1992. PMID: 1622939 Free PMC article.

9

Hereditary hyperferritinemia cataract syndrome: ocular, genetic, and biochemical findings.

Ismail AR, Lachlan KL, Mumford AD, Temple IK, Hodgkins PR. Ismail AR, et al. Among authors: hodgkins pr. Eur J Ophthalmol. 2006 Jan-Feb;16(1):153-60. doi: 10.1177/112067210601600125. Eur J Ophthalmol. 2006. PMID: 16496261

10

Anterior chamber eye anomalies, redundant skin and syndactyly--a new syndrome associated with breakpoints at 2q37.2 and 7q36.3.

Temple IK, Browne C, Hodgkins P. Temple IK, et al. Clin Dysmorphol. 1999 Jul;8(3):157-63. Clin Dysmorphol. 1999. PMID: 10457847

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