[Multiple evanescent white dot syndrome. A diagnostic dilemma]

Autor: C, Vázquez Marouschek, F, López Checa

Publikováno v: Archivos de la Sociedad Espanola de Oftalmologia. 78(8)

We present a patient with multiple evanescent white-dot syndrome (MEWDS). On presentation the patient was not initially diagnosed. The diagnosis was established eighteen months later by the clinical, angiographic and electrophysiologic features. We e

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c31d675add7dd10161994857d1afa70f
https://pubmed.ncbi.nlm.nih.gov/12955626

OHP-002 Financial impact of the use of bevacizumab in the treatment of macular oedema secondary to retinal vein occlusion

Autor: FJ Bautista Paloma, S Flores Moreno, A Villalba Moreno, C Vázquez Marouschek, MA Perez Moreno, ER Alfaro Lara

Publikováno v: European Journal of Hospital Pharmacy. 21:A185.2-A185

Background After the Pharmacy and Therapeutics Committee of a tertiary hospital had evaluated ranibizumab and bevacizumab for the treatment of macular oedema secondary to retinal vein occlusion (RVO) based on the available evidence, the two drugs wer

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8b0a89e1b33f950ecb7c2feb26ca869f
https://doi.org/10.1136/ejhpharm-2013-000436.454

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Deciphering intrafamilial phenotypic variability by exome sequencing in a Bardet-Biedl family.

Autor: González-Del Pozo M; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville, University Hospital Virgen del Rocio/Consejo Superior de Investigaciones Científicas/University of Seville Seville, Spain ; Centre for Biomedical Network Research on Rare Diseases (CIBERER) Seville, Spain., Méndez-Vidal C; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville, University Hospital Virgen del Rocio/Consejo Superior de Investigaciones Científicas/University of Seville Seville, Spain ; Centre for Biomedical Network Research on Rare Diseases (CIBERER) Seville, Spain., Santoyo-Lopez J; Medical Genome Project, Genomics and Bioinformatics Platform of Andalusia (GBPA) Seville, Spain., Vela-Boza A; Medical Genome Project, Genomics and Bioinformatics Platform of Andalusia (GBPA) Seville, Spain., Bravo-Gil N; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville, University Hospital Virgen del Rocio/Consejo Superior de Investigaciones Científicas/University of Seville Seville, Spain., Rueda A; Medical Genome Project, Genomics and Bioinformatics Platform of Andalusia (GBPA) Seville, Spain., García-Alonso L; Department of Computational Genomics, Centro de Investigación Príncipe Felipe (CIPF) Valencia, Spain., Vázquez-Marouschek C; Department of Ophthalmology, University Hospital Virgen del Rocío Seville, Spain., Dopazo J; Medical Genome Project, Genomics and Bioinformatics Platform of Andalusia (GBPA) Seville, Spain ; Department of Computational Genomics, Centro de Investigación Príncipe Felipe (CIPF) Valencia, Spain ; Functional Genomics Node (INB), CIPF Valencia, Spain., Borrego S; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville, University Hospital Virgen del Rocio/Consejo Superior de Investigaciones Científicas/University of Seville Seville, Spain ; Centre for Biomedical Network Research on Rare Diseases (CIBERER) Seville, Spain., Antiñolo G; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville, University Hospital Virgen del Rocio/Consejo Superior de Investigaciones Científicas/University of Seville Seville, Spain ; Centre for Biomedical Network Research on Rare Diseases (CIBERER) Seville, Spain ; Medical Genome Project, Genomics and Bioinformatics Platform of Andalusia (GBPA) Seville, Spain.

Publikováno v: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2014 Mar; Vol. 2 (2), pp. 124-33. Date of Electronic Publication: 2013 Dec 03.