Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 16 de 16
Filtrar
1.
Rev Col Bras Cir ; 50: e20233521, 2023.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-37436282

RESUMEN

INTRODUCTION: cutaneous melanoma (MC) is a malignant neoplasm derived from melanocytic cells with an aggressive behavior. It is usually associated with the multifactorial interaction of genetic susceptibility and environmental exposure, usually ultraviolet radiation. Despite advances in treatment, the disease remains relentless with poor prognosis. Sentinel lymph node (SLN) biopsy is a technique used to screen patients in need of lymph node dissection. OBJECTIVES: to correlate the tumor burden in the SLN with the mortality of patients undergoing SLN biopsy. METHODOLOGY: the medical records and histological slides of patients with MC who underwent SLN biopsy treated at HC-Unicamp from 2001 to 2021 were retrospectively analyzed. The positive SLN were measured according to the size of the tumor infiltration area, for analysis of the depth of invasion (DI), closest proximity to the capsule (CPC) and tumor burden (TB). For statistical analysis, associations between variables were analyzed using Fishers exact test, with post Bonferroni test and Wilcoxon test. RESULTS: 105 records of patients who underwent SLN biopsy of MC were identified. Of these, nine (8.6%) had positive SLN and 81 (77.1%) had negative SLN. The performed lymphadenectomies resulted in 55.6% (n=5) affected, 22.2% (n=2) without disease and 22.2% (n=2) were not performed. Mean CPC, TB, and DI were 0.14mm, 32.10mm and 2.33mm, respectively. Patients with T2 and T3 tumors were more likely to show the SLN affected (p=0.022). No patient with positive SLN died during follow-up. CONCLUSION: patients who presented T3 staging are the ones who most presented positive SLN.


Asunto(s)
Melanoma , Ganglio Linfático Centinela , Neoplasias Cutáneas , Humanos , Melanoma/patología , Neoplasias Cutáneas/patología , Carga Tumoral , Ganglio Linfático Centinela/patología , Estudios Retrospectivos , Rayos Ultravioleta , Metástasis Linfática , Biopsia del Ganglio Linfático Centinela/métodos , Escisión del Ganglio Linfático , Pronóstico , Estadificación de Neoplasias , Melanoma Cutáneo Maligno
2.
Rev. Col. Bras. Cir ; 50: e20233521, 2023. tab, graf
Artículo en Inglés | LILACS-Express | LILACS | ID: biblio-1449189

RESUMEN

ABSTRACT Introduction: cutaneous melanoma (MC) is a malignant neoplasm derived from melanocytic cells with an aggressive behavior. It is usually associated with the multifactorial interaction of genetic susceptibility and environmental exposure, usually ultraviolet radiation. Despite advances in treatment, the disease remains relentless with poor prognosis. Sentinel lymph node (SLN) biopsy is a technique used to screen patients in need of lymph node dissection. Objectives: to correlate the tumor burden in the SLN with the mortality of patients undergoing SLN biopsy. Methodology: the medical records and histological slides of patients with MC who underwent SLN biopsy treated at HC-Unicamp from 2001 to 2021 were retrospectively analyzed. The positive SLN were measured according to the size of the tumor infiltration area, for analysis of the depth of invasion (DI), closest proximity to the capsule (CPC) and tumor burden (TB). For statistical analysis, associations between variables were analyzed using Fishers exact test, with post Bonferroni test and Wilcoxon test. Results: 105 records of patients who underwent SLN biopsy of MC were identified. Of these, nine (8.6%) had positive SLN and 81 (77.1%) had negative SLN. The performed lymphadenectomies resulted in 55.6% (n=5) affected, 22.2% (n=2) without disease and 22.2% (n=2) were not performed. Mean CPC, TB, and DI were 0.14mm, 32.10mm and 2.33mm, respectively. Patients with T2 and T3 tumors were more likely to show the SLN affected (p=0.022). No patient with positive SLN died during follow-up. Conclusion: patients who presented T3 staging are the ones who most presented positive SLN.


RESUMO Introdução: o melanoma cutâneo (MC) é uma neoplasia maligna de comportamento agressivo, derivada das células melanocíticas, geralmente causado pela associação de interação da suscetibilidade genética e a exposição ambiental. A biópsia do linfonodo sentinela (LNS) é um procedimento utilizado para rastreamento de doentes com necessidade ou não de linfadenectomia, diminuindo a exposição do paciente a cirurgias maiores. Objetivos: correlacionar a carga do tumor no LNS com a mortalidade de pacientes com MC. Métodos: foram examinados retrospectivamente prontuários e lâminas histológicas de doentes com MC submetidos a biópsia de LNS atendidos no HC-Unicamp entre o período compreendido de 2001 a 2021. Os LNS positivos foram mensurados quanto ao tamanho da área de infiltração do tumor, para análise da profundidade de invasão (PI), menor proximidade com a cápsula (MPC) e carga do tumor (CT). As associações entre as variáveis foram analisadas pelo teste Exato de Fisher, com pós teste de Bonferroni e Wilcoxon. Resultados: foram identificados 105 pacientes com biópsia de LNS, sendo nove (8,6%) casos com LNS positivo. A média de MDC, CT e PI foram 0,14 mm, 32,10 mm, e 2,33 mm, respectivamente. Doentes com tumores T2 e T3 apresentaram maior chance de acometimento do LNS (p=0,022). Nenhum paciente com LNS positivo foi a óbito durante o acompanhamento. Conclusão: doentes que apresentaram tumores maiores (T2 e T3) apresentaram maior chance de linfonodos sentinelas positivos. Além do tamanho do tumor, a presença de maior carga do tumor demonstrou que os mesmos podem ser beneficiados pela biópsia de LNS.

3.
Sensors (Basel) ; 22(14)2022 Jul 06.
Artículo en Inglés | MEDLINE | ID: mdl-35890747

RESUMEN

Laser-induced breakdown spectroscopy (LIBS) associated with machine learning algorithms (ML) was used to evaluate the Brachiaria seed physiological quality by discriminating the high and low vigor seeds. A 23 factorial design was used to optimize the LIBS experimental parameters for spectral analysis. A total of 120 samples from two distinct cultivars of Brachiaria brizantha seeds exhibiting high vigor (HV) and low vigor (LV) in standard tests were studied. The raw LIBS spectra were normalized and submitted to outlier verification, previously to the reduction data dimensionality from principal component analysis. Supervised machine learning algorithm parameters were chosen by leave-one-out cross-validation in the test samples, and it was tested by external validation using a new set of data. The overall accuracy in external validation achieved 100% for HV and LV discrimination, regardless of the cultivar or the classification algorithm.


Asunto(s)
Brachiaria , Rayos Láser , Aprendizaje Automático , Semillas , Análisis Espectral/métodos
4.
Sci Total Environ ; 837: 155699, 2022 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-35525359

RESUMEN

Double pulse laser-induced breakdown spectroscopy (DP LIBS) has attracted much attention for analyzing trace elements due to its higher sensitivity when compared to single pulse laser-induced breakdown spectroscopy (SP LIBS). However, the development of quantitative methods in LIBS for the analysis of complex samples, such as sediments, is a great challenge due to the matrix effects that are very accentuated in this technique. In this study, different spectral treatments and calibration strategies were investigated to obtain calibration models that allow determinations with satisfactory accuracy and precision of Cr, Cu, and Ni in river sediments from different hydrographic basins. The best model developed for Cr was using MMC without spectral normalization and for Cu and Ni it was using MMC with spectral normalization, and using inverse regression, an increase in the accuracy of the determinations of all analytes was obtained. These models showed limit of quantification (LOQ) of 7.87 mg kg-1, 1.62 mg kg-1, and 2.21 mg kg-1 and root mean square error of prediction (RMSEP) of 7.54 mg kg-1, 14.53 mg kg-1, and 8.29 mg kg-1 for Cr, Cu, and Ni, respectively. Therefore, the models have adequate sensitivity and precision for the quantification of the potentially toxic elements (PTEs) evaluated, since, according to Brazilian legislation, the lower concentration of threshold effect level (TEL) for Cr, Cu, and Ni is <37.3 mg kg-1, <35.7 mg kg-1, and <18 mg kg-1, respectively. The concentrations of Cr, Cu, and Ni determined by DP LIBS allowed to obtain a partial ecological risk assessment of the studied sediments. Also, the chemometric tool Kohonen self-organizing map (KSOM) were used for data interpretation.


Asunto(s)
Ríos , Oligoelementos , Monitoreo del Ambiente/métodos , Rayos Láser , Medición de Riesgo , Ríos/química , Análisis Espectral , Oligoelementos/análisis
5.
J Hazard Mater ; 399: 122831, 2020 11 15.
Artículo en Inglés | MEDLINE | ID: mdl-32531672

RESUMEN

Matrix-matching calibration (MMC), two-point calibration transfer (TP CT), one-point and multi-line calibration (OP MLC), single-sample calibration (SSC) and calibration free (CF) were evaluated in order to overcome matrix effects in laser-induced breakdown spectroscopy (LIBS). These calibration strategies were evaluated for direct determination of Al and Pb in waste printed circuit boards (PCB) using direct solids analysis by LIBS. Each strategy has limitations and advantages of its implementation, for the correction of matrix effects, so that it allows elementary determination with adequate accuracy. The MMC and CF proved to be excellent calibration strategies for the determination of strategic (Al) and toxic (Pb) elements by LIBS, with good recoveries (ranging from 80-120%) and low relative standard deviation (RSD%) values. A detailed discussion of the advantages and limitations of each of these five calibration strategies evaluated for LIBS is presented in this study. Lead concentrations in waste PCB samples are 5-12 times higher than established by Directive 2011/65/EU, and the samples analyzed contain between 3 and 55 g kg-1 Al, being an interesting economic and recycling source for this metal.

6.
Talanta ; 208: 120443, 2020 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-31816804

RESUMEN

This study is dedicated to the direct determination of base (B and Fe) and some rare earth elements (REE; Dy, Gd, Nd, Pr, Sm and Tb) in hard disk magnets. Five calibration strategies were tested and compared. Two of them are related to multivariate calibration: multiple linear regression (MLR) and partial least squares (PLS). Both presented adequate trueness values within a range of 80-120% for almost all analytes. The only exception was Tb, which was probably due to matrix effects. The use of MLR and PLS permits the testing of calibration models in the presence of interference, but matrix effects are not corrected. Because of this, three other univariate calibration methods were also tested and compared: multi-energy calibration (MEC), one-point gravimetric standard addition (OP GSA) and two-point calibration transfer (TP CT). These three calibration approaches permit matrix effects corrections, but an appropriate selection of the blank and standard is mandatory. The standard error obtained ranged from 0.01 to 6% using these univariate calibration methods.

7.
J Pharm Biomed Anal ; 174: 471-478, 2019 Sep 10.
Artículo en Inglés | MEDLINE | ID: mdl-31228850

RESUMEN

This study proposes an analytical procedure for microwave-assisted sample preparation of dietary supplements for athletes using dilute nitric acid solution followed by determination of elemental impurities (As, Cd, Hg and Pb) by inductively coupled plasma mass spectrometry (ICP-MS) according to the United States Pharmacopeia Chapters 2232 and 233. Calibration strategies as internal standardization (IS), multi-isotope calibration (MICal), and one-point standard addition (OP SA) were applied for correction of matrix effects. The optimization of the sample preparation procedure was performed using Doehlert experimental design based on overall desirability results (residual acidity, dissolved organic carbon and recoveries reached for certified reference material of Typical Diet) for each calibration method evaluated. Accuracy was also evaluated by recovery experiments according to the permissible daily exposure specific for each element and samples were spiked with element concentrations of 0.5J and 1.5J in order to check accuracies for As, Cd, Hg and Pb. Recoveries ranged from 82 to 120% using IS, 90 to 125% using MICal, 88 to 120% using OP SA and the repeatability was demonstrated by a precision lower than 10% RSD. Ten samples of dietary sport supplements were analyzed using the three calibration methods evaluated and the concentrations of As, Cd and Pb determined in eight samples were lower than the limits established by the Chapter 2232.


Asunto(s)
Arsénico/análisis , Cadmio/análisis , Suplementos Dietéticos/análisis , Plomo/análisis , Mercurio/análisis , Microondas , Ácido Nítrico/química , Calibración , Límite de Detección , Espectrometría de Masas , Estándares de Referencia , Reproducibilidad de los Resultados , Oligoelementos/análisis
8.
Food Chem ; 273: 91-98, 2019 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-30292381

RESUMEN

This study aims to develop methods for determination of Ca, K, Mg and Na by laser-induced breakdown spectroscopy (LIBS) and Ca, K, Mg, Na, P, S, Fe and Zn by wavelength dispersive X-ray fluorescence (WDXRF) in pressed pellets bivalve mollusks. LIBS and WDXRF calibration models were built with references values determined by inductively coupled plasma optical emission spectrometry (ICP OES) after acid digestion. The calibration models for LIBS and WDXRF were obtained from 28 samples (14 for calibration and 14 for validation). It was possible to implement a validation between LIBS and WDXRF methods for elements Ca, K, Mg and Na. The proposed calibration model obtained using LIBS and WDXRF data presented a good correlation with reference values obtained by ICP OES.


Asunto(s)
Bivalvos/química , Metales/análisis , Mariscos/análisis , Análisis Espectral/métodos , Animales , Calcio/análisis , Calibración , Análisis de los Alimentos/métodos , Rayos Láser , Espectrometría de Fluorescencia/métodos , Rayos X
11.
Orphanet J Rare Dis ; 12(1): 155, 2017 09 15.
Artículo en Inglés | MEDLINE | ID: mdl-28915903

RESUMEN

BACKGROUND: We aim to delineate the progression of cerebellar syndrome in children with phosphomannomutase-deficiency (PMM2-CDG) using the International Cooperative Ataxia Rating Scale (ICARS). We sought correlation between cerebellar volumetry and clinical situation. We prospectively evaluated PMM2-CDG patients aged from 5 to 18 years through ICARS at two different time points set apart by at least 20 months. We reviewed available MRIs and performed volumetric analysis when it was possible. RESULTS: From the eligible 24, four patients were excluded due to severe mental disability (n = 2) and supratentorial lesions (n = 2). Two different ICARS evaluations separated by more than 20 months were available for 14 patients showing an improvement in the cerebellar syndrome: ICARS1: 35.71 versus ICARS2: 30.07 (p < 0.001). When we considered time, we saw an improvement of 2.64 points in the ICARS per year with an SD of 1.97 points (p < 0.001). The ICARS subscales results improved with time, reaching statistical significance in "Posture and gait" (p < 0.001), "Kinetic functions" (p = 0.04) and "Speech abnormalities" (p = 0.045). We found a negative correlation between the ICARS results and total cerebellar volume (r = -0.9, p = 0.037) in a group of five patients with available volumetric study, meaning that the higher the ICARS score, the more severe was the cerebellar atrophy. CONCLUSIONS: Our study shows a stabilization or mild improvement in the cerebellar functions of paediatric PMM2-CDG patients despite cerebellar volume loss. ICARS is a valid scale to quantify the evolution of cerebellar syndrome in PMM2-CDG patients. The availability of ICARS and other reliable and sensitive follow-up tools may prove essential for the evaluation of potential therapies.


Asunto(s)
Enfermedades Cerebelosas/diagnóstico , Enfermedades Cerebelosas/enzimología , Fosfotransferasas (Fosfomutasas)/deficiencia , Adolescente , Enfermedades Cerebelosas/patología , Niño , Preescolar , Femenino , Humanos , Masculino , Neuroimagen , Fosfotransferasas (Fosfomutasas)/genética
13.
J Inherit Metab Dis ; 40(5): 709-713, 2017 09.
Artículo en Inglés | MEDLINE | ID: mdl-28341975

RESUMEN

OBJECTIVE: We aim to delineate the progression of cerebellar atrophy (the primary neuroimaging finding) in children with phosphomannomutase-deficiency (PMM2-CDG) by analyzing longitudinal MRI studies and performing cerebellar volumetric analysis and a 2D cerebellar measurement. METHODS: Statistical analysis was used to compare MRI measurements [midsagittal vermis relative diameter (MVRD) and volume] of children with PMM2-CDG and sex- and age-matched controls, and to determine the rate of progression of cerebellar atrophy at different ages. RESULTS: Fifty MRI studies of 33 PMM2-CDG patients were used for 2D evaluation, and 19 MRI studies were available for volumetric analysis. Results from a linear regression model showed that patients have a significantly lower MVRD and cerebellar volume compared to controls (p < 0.001 and p < 0.001 respectively). There was a significant negative correlation between age and MVRD for patients (p = 0.014). The rate of cerebellar atrophy measured by the loss of MVRD and cerebellar volume per year was higher at early ages (r = -0.578, p = 0.012 and r = -0.323, p = 0.48 respectively), particularly in patients under 11 years (p = 0.004). There was a significant positive correlation between MVRD and cerebellar volume in PMM2-CDG patients (r = 0.669, p = 0.001). CONCLUSIONS: Our study quantifies a progression of cerebellar atrophy in PMM2-CDG patients, particularly during the first decade of life, and suggests a simple and reliable measure, the MVRD, to monitor cerebellar atrophy. Quantitative measurement of MVRD and cerebellar volume are essential for correlation with phenotype and outcome, natural follow-up, and monitoring in view of potential therapies in children with PMM2-CDG.


Asunto(s)
Atrofia/metabolismo , Atrofia/patología , Cerebelo/metabolismo , Cerebelo/patología , Fosfotransferasas (Fosfomutasas)/deficiencia , Fosfotransferasas (Fosfomutasas)/metabolismo , Niño , Estudios de Cohortes , Progresión de la Enfermedad , Femenino , Humanos , Estudios Longitudinales , Imagen por Resonancia Magnética/métodos , Masculino
14.
Talanta ; 152: 457-62, 2016 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-26992542

RESUMEN

A new method is proposed for the simultaneous determination of Mo and Ni in plant materials by high-resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS GFAAS), employing direct solid sample analysis (DSS) and internal standardization (IS). Cobalt was used as internal standard to minimize matrix effects during Ni determinations, enabling the use of aqueous standards for calibration. Correlation coefficients for the calibration curves were typically better than 0.9937. The performance of the method was checked by analysis of six plant certified reference materials, and the results for Mo and Ni were in agreement with the certified values (95% confidence level, t-test). Analysis was made of different types of plant materials used as renewable sources of energy, including sugarcane leaves, banana tree fiber, soybean straw, coffee pods, orange bagasse, peanut hulls, and sugarcane bagasse. The concentrations found for Mo and Ni ranged from 0.08 to 0.63 ng mg(-1) and from 0.41 to 6.92 ng mg(-1), respectively. Precision (RSD) varied from 2.1% to 11% for Mo and from 3.7% to 10% for Ni. Limits of quantification of 0.055 and 0.074 ng were obtained for Mo and Ni, respectively.


Asunto(s)
Grafito/química , Molibdeno/análisis , Níquel/análisis , Plantas/química , Espectrofotometría Atómica/normas , Calibración , Cobalto/análisis , Calor , Hojas de la Planta/química , Estándares de Referencia , Factores de Tiempo
15.
Orphanet J Rare Dis ; 10: 138, 2015 Oct 26.
Artículo en Inglés | MEDLINE | ID: mdl-26502900

RESUMEN

BACKGROUND: Phosphomannomutase deficiency (PMM2-CDG) is the most frequent congenital disorder of glycosylation. The cerebellum is nearly always affected in PMM2-CDG patients, a cerebellar atrophy progression is observed, and cerebellar dysfunction is their main daily functional limitation. Different therapeutic agents are under development, and clinical evaluation of drug candidates will require a standardized score of cerebellar dysfunction. We aim to assess the validity of the International Cooperative Ataxia Rating Scale (ICARS) in children and adolescents with genetically confirmed PMM2-CDG deficiency. We compare ICARS results with the Nijmegen Pediatric CDG Rating Scale (NPCRS), neuroimaging, intelligence quotient (IQ) and molecular data. METHODS: Our observational study included 13 PMM2-CDG patients and 21 control subjects. Ethical permissions and informed consents were obtained. Three independent child neurologists rated PMM2-CDG patients and control subjects using the ICARS. A single clinician administered the NPCRS. All patients underwent brain MRI, and the relative diameter of the midsagittal vermis was measured. Psychometric evaluations were available in six patients. The Mann-Whitney U test was used to compare ICARS between patients and controls. To evaluate inter-observer agreement in patients' ICARS ratings, intraclass correlation coefficients (ICC) were calculated. ICARS internal consistency was evaluated using Cronbach's alpha. Spearman's rank correlation coefficient test was used to correlate ICARS with NPCRS, midsagittal vermis relative diameter and IQ. RESULTS: ICARS and ICARS subscores differed between patients and controls (p < 0.001). Interobserver agreement of ICARS was "almost perfect" (ICC = 0.99), with a "good" internal reliability (Cronbach's alpha = 0.72). ICARS was significantly correlated with the total NPCRS score (rs 0.90, p < 0.001). However, there was no agreement regarding categories of severity. Regarding neuroimaging, inverse correlations between ICARS and midsagittal vermis relative diameter (rs -0.85, p = 0.003) and IQ (rs -0.94, p = 0.005) were found. Patients bearing p.E93A, p.C241S or p.R162W mutations presented a milder phenotype. CONCLUSIONS: ICARS is a reliable instrument for assessment of PMM2-CDG patients, without significant inter-rater variability. Despite our limited sample size, the results show a good correlation between functional cerebellar assessment, IQ and neuroimaging. For the first a correlation between ICARS, neuroimaging and IQ in PMM2-CDG patients has been demonstrated.


Asunto(s)
Ataxia Cerebelosa/diagnóstico , Cerebelo/patología , Trastornos Congénitos de Glicosilación/diagnóstico , Fosfotransferasas (Fosfomutasas)/deficiencia , Índice de Severidad de la Enfermedad , Adolescente , Ataxia Cerebelosa/enzimología , Ataxia Cerebelosa/genética , Niño , Preescolar , Trastornos Congénitos de Glicosilación/enzimología , Trastornos Congénitos de Glicosilación/genética , Femenino , Humanos , Masculino , Fosfotransferasas (Fosfomutasas)/genética
16.
Invest Ophthalmol Vis Sci ; 51(7): 3509-14, 2010 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20237253

RESUMEN

PURPOSE. Primary open-angle glaucoma (POAG) is a complex disease with a genetic architecture that can be simplified through the investigation of individual traits underlying disease risk. It has been well studied in twin models, and this study was undertaken to investigate the heritability of some of these key endophenotypes in extended pedigrees. METHODS. These data are derived from a large, multicenter study of extended, Caucasian POAG families from Australia and the United States. The study included 1181 people from 22 extended pedigrees. Variance components modeling was used to determine the heritabilities of maximum intraocular pressure (IOP), maximum vertical cup-to-disc ratio (VCDR), and mean central corneal thickness (CCT). Bivariate quantitative genetic analysis between these eye-related phenotypes and POAG itself was performed to determine whether any of these traits represent true endophenotypes. RESULTS. Heritability estimates for IOP, VCDR, and CCT (0.42, 0.66, and 0.72, respectively) were significant and show strong concordance with data in previous studies. Bivariate analysis revealed that both IOP (RhoG = 0.80; P = 9.6 x 10(-6)) and VCDR (RhoG = 0.76; P = 4.8 x 10(-10)) showed strong evidence of genetic correlation with POAG susceptibility. These two traits also correlated genetically with each other (RhoG = 0.45; P = 0.0012). Alternatively, CCT did not correlate genetically with risk of POAG. CONCLUSIONS. All the proposed POAG-related traits have genetic components. However, the significant genetic correlations observed between IOP, VCDR, and POAG itself suggest that they most likely represent true endophenotypes that could aid in the identification of genes underlying POAG susceptibility. CCT did not correlate genetically with disease and is unlikely to be a useful surrogate endophenotype for POAG.


Asunto(s)
Córnea/patología , Predisposición Genética a la Enfermedad , Glaucoma de Ángulo Abierto/genética , Presión Intraocular/genética , Disco Óptico/patología , Femenino , Estudios de Asociación Genética , Ligamiento Genético , Glaucoma de Ángulo Abierto/diagnóstico , Humanos , Masculino , Persona de Mediana Edad , Fibras Nerviosas/patología , Linaje , Fenotipo , Células Ganglionares de la Retina/patología , Factores de Riesgo , Tonometría Ocular
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA