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Iron deficiency in infancy: applying a physiologic framework for prediction
(AMER SOC CLINICAL NUTRITION, 2006-12)
Background: Infants aged 6-24 mo are at high risk of iron deficiency. Numerous studies worldwide have sought to identify predictors of iron deficiency in this age group.
Objective: The objectives of the study were to apply ...
Descrição do conceito de deficiência a partir da mídia cinematográfica: uma análise comportamental
(2010-07-23)
This work pointed out forming elements from the conception of special necessities that the media show the audience by the movies. An expression description has established special needs and they were identified as keywords ...
Descrição do conceito de deficiência a partir da mídia cinematográfica: uma análise comportamental
(2010-07-23)
This work pointed out forming elements from the conception of special necessities that the media show the audience by the movies. An expression description has established special needs and they were identified as keywords ...
Educação inclusiva e inclusão social
(Universidade Federal de Santa MariaBrasilUFSMCentro de Ciências Sociais e Humanas, 2016-01-05)
The article makes a survey about the legal principles and protections of Inclusive Education in Brazil. We live in a country that seeks to live diversity in general, for this it is necessary to understand the guiding ...
Image segmentation with artificial neural network for nutrient deficiency in cotton crop
(2014-01-01)
The leaf analysis in a crop can present the need of a nutrient determined in the plant. The macronutrients deficiency in the cotton crop can be identified by specific type of colors variation by leaves images. Early ...
Rare detection of bordetella pertussis pertactin-deficient strains in Argentina
(Centers Disease Control, 2019-11)
Pertussis resurgence had been attributed to waning vaccine immunity and Bordetella pertussis adaptation to escape vaccine-induced immunity. Circulating bacteria differ genotypically from strains used in production of ...
Lesch-Nyhan disease and its variants: Phenotypic and mutation spectrum of Hypoxanthine-Guanine Phosphoribosyltransferase deficiency in Argentine patients
(Scielo, 2021-03)
Hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency is a disorder of purine metabolism responsible for Lesch-Nyhan Disease (LND) and its variants, HPRT-related hyperuricemia with neurologic dysfunction (HND) ...