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1.
Photochem Photobiol ; 78(6): 603-6, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14743870

RESUMEN

Aspects of different calibration procedures for erythemally weighing broadband radiometers are presented in this study. These instruments are common in projects dealing with ultraviolet radiation effects on humans. Many erythemally weighing broadband radiometers are still operated using a single calibration factor (cf) that is provided with the instrument. The individual characteristics of every instrument are strongly dependent on the total ozone amount and the solar elevation. Therefore, a calibration procedure also has to take into account the ozone concentrations and the solar elevation to compensate for the effects of the individual characteristics and to provide comparable measurements. Given the variation of the ozone concentrations and the solar elevation, an individual cf has to be calculated for every measurement. Using a simplified version of the calibration procedure, which is presented in this study, can lessen this effort. Taking into account the relevant meteorological conditions for a measuring site, a single cf is calculated to compensate the individual characteristics of the instruments and therefore deliver comparable measurements with less effort.


Asunto(s)
Monitoreo de Radiación/métodos , Energía Solar , Rayos Ultravioleta , Calibración , Ozono , Monitoreo de Radiación/instrumentación
2.
Clin Genet ; 63(6): 462-75, 2003 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-12786753

RESUMEN

Predictive and pre-natal testing for Huntington's Disease (HD) has been available since 1987. Initially this was offered by linkage analysis, which was surpassed by the advent of the direct mutation test for HD in 1993. Direct mutation analysis provided an accurate test that not only enhanced predictive and pre-natal testing, but also permitted the diagnostic testing of symptomatic individuals. The objective of this study was to investigate the uptake, utilization, and outcome of predictive, pre-natal and diagnostic testing in Canada from 1987 to April 1, 2000. A retrospective design was used; all Canadian medical genetics centres and their affiliated laboratories offering genetic testing for HD were invited to participate. A total of 15 of 22 centres (68.2%), currently offering or ever having offered genetic testing for HD, responded, providing data on test results, demographics, and clinical history. A total of 1061 predictive tests, 15 pre-natal tests, and 626 diagnostic tests were performed. The uptake for predictive testing was approximately 18% of the estimated at-risk Canadian population, ranging from 12.5% in the Maritimes to 20.7% in British Columbia. There appears to have been a decline in the rate of testing in recent years. Of the predictive tests, 45.0% of individuals were found to have an increased risk, and a preponderance of females (60.2%) sought testing. A greater proportion of those at < or = 25% risk sought predictive testing once direct CAG mutation analysis had become available (10.9% after mutation analysis vs 4.7% before mutation analysis, p = 0.0077). Very few pre-natal tests were requested. Of the 15 pre-natal tests, 12 had an increased risk, resulting in termination of pregnancy in all but one. Diagnostic testing identified 68.5% of individuals to be positive by mutation analysis, while 31.5% of those with HD-like symptoms were not found to have the HD mutation. The positive diagnostic tests included 24.5% of individuals with no known prior family history of HD.


Asunto(s)
Enfermedad de Huntington/diagnóstico , Enfermedad de Huntington/genética , Diagnóstico Prenatal , Adolescente , Adulto , Edad de Inicio , Anciano , Anciano de 80 o más Años , Canadá , Femenino , Humanos , Masculino , Persona de Mediana Edad , Embarazo , Estudios Retrospectivos , Expansión de Repetición de Trinucleótido
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