Search Results - "Morillo, María José"
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Characterization of Electrospun BDMC-Loaded PLA Nanofibers with Drug Delivery Function and Anti-Inflammatory Activity
Published in International journal of molecular sciences (01-06-2023)“…Controlled drug release systems are the subject of many investigations to achieve the therapeutic effect of drugs. They have numerous advantages, such as…”
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The emerging role of mesenchymal stem cell-derived extracellular vesicles to ameliorate hippocampal NLRP3 inflammation induced by binge-like ethanol treatment in adolescence
Published in Neural regeneration research (01-04-2025)“…JOURNAL/nrgr/04.03/01300535-202504000-00030/figure1/v/2024-07-06T104127Z/r/image-tiff Our previous studies have reported that activation of the NLRP3 (NOD-,…”
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3
Expanding the phenotype of THRB : a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing variant
Published in Frontiers in cell and developmental biology (21-07-2023)“…Inherited retinal dystrophies (IRDs) are a clinically and genetically heterogeneous group of disorders that often severely impair vision. Some patients…”
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A comprehensive WGS-based pipeline for the identification of new candidate genes in inherited retinal dystrophies
Published in Npj genomic medicine (04-03-2022)“…To enhance the use of Whole Genome Sequencing (WGS) in clinical practice, it is still necessary to standardize data analysis pipelines. Herein, we aimed to…”
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All is land, but not all is landscape: social discourses around the landscape
Published in Landscape research (04-07-2023)“…Political and academic discourses generally argue that it is possible for all land to be viewed as landscape. Research into social discourse about the…”
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Multidisciplinary approach to inherited causes of dual sensory impairment
Published in Graefe's archive for clinical and experimental ophthalmology (01-03-2024)“…Purpose This article presents a review of the main causes of inherited dual sensory impairment (DSI) with an emphasis on the multidisciplinary approach…”
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The Effects of Parenteral K1 Administration in Pseudoxanthoma Elasticum Patients Versus Controls. A Pilot Study
Published in Frontiers in medicine (16-04-2018)“…Pseudoxanthoma elasticum (PXE) is a rare disease caused by mutations in the ABCC6 gene. Vitamin K1 is involved in the posttranslational carboxylation of some…”
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Novel BEST1 mutations and clinical characteristics of autosomal recessive bestrophinopathy in a Spanish patient
Published in European journal of ophthalmology (01-09-2022)“…Purpose: To describe the clinical and genetic characteristics (novel mutation in BEST1 gene) of a Spanish patient with autosomal recessive bestrophinopathy…”
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Macular choroidal thickness in patients with pseudoxanthoma elasticum measured by enhanced-depth imaging spectral-domain optical coherence tomography
Published in International ophthalmology (01-07-2020)“…Background/objectives To analyze macular choroidal thickness in patients with pseudoxanthoma elasticum (PXE) by enhanced depth imaging optical coherence…”
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Unusual clinical phenotype of Stargardt disease
Published in Arquivos brasileiros de oftalmologia (01-01-2021)“…Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phenotypes have also been associated with mutations in this gene…”
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Dissecting the role of EYS in retinal degeneration: clinical and molecular aspects and its implications for future therapy
Published in Orphanet journal of rare diseases (17-05-2021)“…Mutations in the EYS gene are one of the major causes of autosomal recessive retinitis pigmentosa. EYS-retinopathy presents a severe clinical phenotype, and…”
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Role of mitochondria ROS generation in ethanol-induced NLRP3 inflammasome activation and cell death in astroglial cells
Published in Frontiers in cellular neuroscience (01-08-2014)“…Toll-like receptors (TLRs) and NOD-like receptors (NLRs) are innate immunity sensors that provide an early/effective response to pathogenic or injury…”
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Posterior microphthalmos, retinitis pigmentosa, and foveoschisis caused by a mutation in the MFRP gene: a familial study
Published in Ophthalmic genetics (04-05-2019)“…Background: To characterize the phenotype and genotype of a rare syndrome associating posterior microphthalmos (PM), retinitis pigmentosa (RP), and…”
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Magnetic reconnection, plasmoids and numerical resolution
Published 13-06-2024“…Explaining fast magnetic reconnection in electrically conducting plasmas has been a theoretical challenge in plasma physics since its first description by…”
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PP-12 ARTIFICIAL COLLAPSE OF HUMAN BLASTOCYSTS, BEFORE VITRIFICATION, IMPROVES SURVIVAL AND PREGNANCY RATES
Published in Reproductive biomedicine online (01-04-2012)Get full text
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The Effect of Peripapillary Detachment on Retinal Nerve Fiber Layer Measurement by Spectral Domain Optical Coherence Tomography in High Myopia
Published in Ophthalmologica (Basel) (01-01-2015)“…The aim of this study was to investigate the repercussions of peripapillary detachment on retinal nerve fiber layer (RNFL) measurements in patients with highly…”
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Fenótipo clínico incomum da doença de Stargardt
Published in Arquivos brasileiros de oftalmologia (2021)Get full text
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Unusual clinical phenotype of Stargardt disease
Published in Arquivos brasileiros de oftalmologia (2021)“…ABSTRACT Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phenotypes have also been associated with mutations in…”
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Chorioretinal Atrophy after Spontaneous Resolution of Myopic Foveoschisis
Published in Case reports in ophthalmological medicine (01-01-2014)“…Myopic foveoschisis is one of the major complications of pathologic myopia, and it was most recently identified by new imaging modalities. During the natural…”
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Two- and three-dimensional topographic analysis of pathologically myopic eyes with dome-shaped macula and inferior staphyloma by spectral domain optical coherence tomography
Published in Graefe's archive for clinical and experimental ophthalmology (01-05-2017)“…Purpose To investigate the posterior anatomical structure of pathologically myopic eyes with dome-shaped macula and inferior staphyloma using spectral domain…”
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