منابع مشابه
MASCARA (Manejo del Síndrome Coronario Agudo. Registro Actualizado) study. General findings.
INTRODUCTION AND OBJECTIVES To investigate the clinical characteristics and treatment of acute coronary syndromes (ACS), and to determine the effects of an early invasive strategy (EIS) in non-ST-elevation ACS (NSTEACS) and of primary percutaneous coronary intervention (PCI) in ST-elevation ACS (STEACS). METHODS Data were collected prospectively for 9 months during 2004-2005 from 50 hospitals...
متن کاملPrevalencia de alteraciones estructurales
Resumen Intro duc ción: Los es tu dios ar te ria les no-in va si vos se em plean en adul tos para va lo ra ción de daño de ór ga no blan co, re-cla si fi ca ción de ries go car dio vas cu lar y/o de tec ción tem pra na de al te ra cio nes en es truc tu ra y fun ción ar te rial. Re cien te men te, se re co men dó su em pleo en ni ños, dado que per mi ti rían de tec tar aque llos con ma yor sus c...
متن کاملMaxillary Sinus Septa Prevalence and Morphology-Computed Tomography Based Analysis Prevalencia y Morfología del Septo del Seno Maxilar. Análisis Basado en Estudios de Tomografía Computadorizada
The aim of this study was to examine the prevalence, location and morphology of maxillary sinus septa, and in particular sagittally orientated forms, which cannot be visualized by classic 2D x-rays. Thereby authors would like to provide information about the potential patient group, to be referred for the computed tomography scan before sinus lift procedure. The analysis was based on 216 comput...
متن کاملSíndrome de Cogan Reese Cogan Reese syndrome
Estudo realizado para descrever um caso da síndrome de Cogan Reese. Paciente do sexo feminino, 55 anos, com diagnóstico de síndrome de Cogan Reese. Melhor acuidade visual de 0,67 em olho direito e 0,2 em olho esquerdo. Pelo exame biomicroscópico não se detectou anormalidades no olho direito. No olho esquerdo haviam nódulos pigmentados na superfície anterior da íris, irregularidades corneanas e ...
متن کاملFragile X Syndrome Síndrome de X
190 Abstract Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full mutation (greater than 200 CGG repeats), in the FMR1 gene locus Xq27.3; which leads to an hypermethylated region in the gene promoter therefore silencing it and lowering the expression levels of FMRP, a protein involved in synaptic plasticity and maturation. Individuals with FXS present w...
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ژورنال
عنوان ژورنال: Revista Alergia México
سال: 2014
ISSN: 2448-9190,0002-5151
DOI: 10.29262/ram.v61i1.16