Kamron N Khan

Kamron N Khan

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Kamron N Khan

Kamron N Khan

Publications by authors named "Kamron N Khan"

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Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options.

Br J Ophthalmol 2020 Apr 8;104(4):451-460. Epub 2019 Nov 8.

Moorfields Eye Hospital, London, UK

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http://dx.doi.org/10.1136/bjophthalmol-2019-315086DOI Listing
April 2020

Loss-of-Function Mutations in the CFH Gene Affecting Alternatively Encoded Factor H-like 1 Protein Cause Dominant Early-Onset Macular Drusen.

Ophthalmology 2019 10 21;126(10):1410-1421. Epub 2019 Mar 21.

Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom; Manchester Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, St. Mary's Hospital, Manchester, United Kingdom. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S01616420183317
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http://dx.doi.org/10.1016/j.ophtha.2019.03.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856713PMC
October 2019

Retinopathy Associated with Biallelic Mutations in PYGM (McArdle Disease).

Ophthalmology 2019 02 11;126(2):320-322. Epub 2018 Oct 11.

UCL Institute of Ophthalmology, University College London, London, UK; Genetics and Medical Retina Services, Moorfields Eye Hospital, London, UK.

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https://linkinghub.elsevier.com/retrieve/pii/S01616420183225
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http://dx.doi.org/10.1016/j.ophtha.2018.09.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6347563PMC
February 2019

Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.

Ophthalmology 2018 05 6;125(5):735-746. Epub 2018 Jan 6.

Department of Genetics, University College London Institute of Ophthalmology, University College London, London, United Kingdom; Medical Retina Service, Moorfields Eye Hospital, London, United Kingdom. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S01616420173253
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http://dx.doi.org/10.1016/j.ophtha.2017.11.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917070PMC
May 2018

THE FUNDUS PHENOTYPE ASSOCIATED WITH THE p.Ala243Val BEST1 MUTATION.

Retina 2018 Mar;38(3):606-613

University College London Institute of Ophthalmology, University College London, London, Unite Kingdom.

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http://Insights.ovid.com/crossref?an=00006982-201803000-0002
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http://dx.doi.org/10.1097/IAE.0000000000001569DOI Listing
March 2018

DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISM.

Retina 2018 Mar;38(3):620-628

University College London Institute of Ophthalmology, University College London, London, United Kingdom.

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http://dx.doi.org/10.1097/IAE.0000000000001570DOI Listing
March 2018

NORMAL ELECTROOCULOGRAPHY IN BEST DISEASE AND AUTOSOMAL RECESSIVE BESTROPHINOPATHY.

Retina 2018 Feb;38(2):379-386

University College London Institute of Ophthalmology, University College London, London, United Kingdom.

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http://dx.doi.org/10.1097/IAE.0000000000001523DOI Listing
February 2018

Vitamin A deficiency due to bi-allelic mutation of RBP4: There's more to it than meets the eye.

Ophthalmic Genet 2017 Sep-Oct;38(5):465-466. Epub 2016 Nov 28.

a University College London Institute of Ophthalmology , University College London , London , UK.

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http://dx.doi.org/10.1080/13816810.2016.1227453DOI Listing
December 2017

FUNCTIONAL AND ANATOMICAL OUTCOMES OF CHOROIDAL NEOVASCULARIZATION COMPLICATING BEST1-RELATED RETINOPATHY.

Retina 2017 Jul;37(7):1360-1370

*University College London Institute of Ophthalmology, University College London, London, United Kingdom; †Medical Retina Service, Moorfields Eye Hospital, London, United Kingdom; ‡Department of Ophthalmology, Leeds Institute of Molecular Medicine, St James' University Hospital, Leeds, United Kingdom; and §Department of Ophthalmology, University of California San Francisco Medical School, San Francisco, California.

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http://dx.doi.org/10.1097/IAE.0000000000001357DOI Listing
July 2017

Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy.

JAMA Ophthalmol 2017 04;135(4):339-347

Genomic Medicine, Division of Evolution and Genomic Sciences, Faculty of Biology, Medicines and Health, University of Manchester, Manchester Academic Health Science Centre (MAHSC), Manchester, England2Manchester Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, MAHSC, Saint Mary's Hospital, Manchester, England.

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http://dx.doi.org/10.1001/jamaophthalmol.2017.0046DOI Listing
April 2017

Clinical and Genetic Features of Choroideremia in Childhood.

Ophthalmology 2016 10 6;123(10):2158-65. Epub 2016 Aug 6.

University College London Institute of Ophthalmology, University College London, London, United Kingdom; Medical Retina Service, Moorfields Eye Hospital, London, United Kingdom.

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http://dx.doi.org/10.1016/j.ophtha.2016.06.051DOI Listing
October 2016

Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy.

JAMA Ophthalmol 2016 Sep;134(9):992-1000

UCL (University College of London) Institute of Ophthalmology, London, England2Moorfields Eye Hospital, London, England.

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http://dx.doi.org/10.1001/jamaophthalmol.2016.2089DOI Listing
September 2016

Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes.

Prog Retin Eye Res 2016 07 10;53:70-106. Epub 2016 May 10.

University College London, Institute of Ophthalmology, 11-43 Bath Street, London EC1V 9EL, UK; Medical Retina Service, Moorfields Eye Hospital, 162 City Road, London EC1V 2PD, UK; Department of Ophthalmology, UCSF School of Medicine, San Francisco, CA 94143, USA.

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http://dx.doi.org/10.1016/j.preteyeres.2016.04.008DOI Listing
July 2016

Correspondence.

Retina 2014 Jan;34(1):e1

*Leeds Institute of Molecular Medicine, Leeds, United Kingdom †Calderdale Royal Infirmary, Halifax, United Kingdom.

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https://insights.ovid.com/crossref?an=00006982-201401000-000
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http://dx.doi.org/10.1097/IAE.0000000000000030DOI Listing
January 2014

Patterns of inheritance, not always easily visible.

BMJ 2013 Nov 6;347:f6610. Epub 2013 Nov 6.

Section of Ophthalmology and Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, St James's University Hospital, Leeds LS9 7TF, UK.

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http://dx.doi.org/10.1136/bmj.f6610DOI Listing
November 2013

A cautious approach to interpreting retrospective data.

Br J Ophthalmol 2013 Oct 21;97(10):1358. Epub 2013 Aug 21.

Department of ophthalmology, Leeds Institute of Molecular Medicine, , Leeds, UK.

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http://dx.doi.org/10.1136/bjophthalmol-2013-304051DOI Listing
October 2013

Changing the status quo bias.

Br J Ophthalmol 2011 Jul 17;95(7):1034. Epub 2011 Jan 17.

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http://dx.doi.org/10.1136/bjo.2010.200428DOI Listing
July 2011