David Rivera-de Parra

David Rivera-de la Parra

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David Rivera-de Parra

David Rivera-de la Parra

Publications by authors named "David Rivera-de la Parra"

7Publications

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1PubMed Central Citations

PARACENTRAL ACUTE MIDDLE MACULOPATHY IN PURTSCHER RETINOPATHY.

Retin Cases Brief Rep 2017 Dec 27. Epub 2017 Dec 27.

Retina Division,Asociación Para Evitar la Ceguera en México I.A.P., México City, México.

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http://dx.doi.org/10.1097/ICB.0000000000000696DOI Listing
December 2017

MULTICOLOR SCANNING LASER IMAGING IN LIPEMIA RETINALIS.

Retin Cases Brief Rep 2017 Winter;11 Suppl 1:S132-S135

*Centro de atención integral del paciente con diabetes, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico; †Instituto de Oftalmología "Fundación Conde de Valenciana" I.A.P., Mexico City, Mexico; ‡Florida State University College of Medicine, Bonita Springs, Florida; §Arizona Eye Consultants, Tucson, Arizona; and ¶Jules Stein Eye Institute, University of California Los Angeles, Los Angeles, California.

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http://dx.doi.org/10.1097/ICB.0000000000000469DOI Listing
June 2017

CHEMOTHERAPEUTIC NADIR-ASSOCIATED RETINOPATHY.

Retin Cases Brief Rep 2017 Winter;11 Suppl 1:S38-S40

*Centro de atención integral del paciente con diabetes, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico city, Mexico; and†Instituto de Oftalmología "Fundación Conde de Valenciana" I.A.P., Mexico city, Mexico.

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http://dx.doi.org/10.1097/ICB.0000000000000396DOI Listing
March 2017

Identification of unsuspected Wolfram syndrome cases through clinical assessment and WFS1 gene screening in type 1 diabetes mellitus patients.

Gene 2015 Jul 17;566(1):63-7. Epub 2015 Apr 17.

Department of Genetics-Research Unit, Institute of Ophthalmology "Conde de Valenciana", Mexico City, Mexico; Department of Biochemistry, Faculty of Medicine, UNAM, Mexico City, Mexico. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2015.04.040DOI Listing
July 2015

Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome.

Cornea 2014 Mar;33(3):247-51

*Section of Ophthalmology and Neuroscience, Leeds Institute of Biomedical and Clinical Sciences, University of Leeds, Leeds, United Kingdom; †Department of Ophthalmology, St James's University Hospital, Leeds, United Kingdom; ‡Department of Biochemistry, Faculty of Medicine, National Autonomous University of Mexico (UNAM), Mexico City, Mexico; §Department of Genetics, Institute of Ophthalmology "Conde de Valenciana," Mexico City, Mexico; and ¶Department of Ophthalmology, Bradford Royal Infirmary, Bradford, United Kingdom.

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http://dx.doi.org/10.1097/ICO.0000000000000041DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195577PMC
March 2014

A new GJA1 (connexin 43) mutation causing oculodentodigital dysplasia associated to uncommon features.

Ophthalmic Genet 2007 Dec;28(4):198-202

Research Unit, Institute of Ophthalmology Conde de Valenciana, Mexico City, Mexico.

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http://dx.doi.org/10.1080/13816810701538620DOI Listing
December 2007