Results 161 to 170 of about 7,701,914 (336)
Que professoras/professores estamos sendo, em tempos difíceis como os de hoje, quando a escola caminha para funcionar, cada vez mais como empresa, sendo a educação, esvaziada de seu significado humano, sua mercadoria? Nesse processo de formação e nas relações de trabalho vividas, quem estamos sendo? Quem estamos chegando a ser?
openaire +1 more source
Poster advertising Summer Course in Descriptive Astronomy at Central College and a variety of equipment housed within the Observatory. Top picture is of exterior of Morrison Observatory; bottom picture is of the 17-foot Clark refractor ...
Central Methodist University; Smiley Memorial Library
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ABSTRACT Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%–5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce in the literature.
Gabriela Roldão Correia‐Costa +4 more
wiley +1 more source
ABSTRACT Mucopolysaccharidoses (MPS) are lysosomal storage disorders characterized by the accumulation of glycosaminoglycans (GAGs), which can lead to cytoplasmic alterations in leukocytes. The objective of this study was to characterize leukocyte inclusions in patients with different types of MPS and assess their diagnostic relevance.
Márcio A. W. Melo +5 more
wiley +1 more source
TUMOR ESTROMAL GASTROINTESTINAL COMO DIAGNÓSTICO DE MASSA DE SEPTO RETOVAGINAL
Priscilla Martins +6 more
doaj +1 more source
Concierto interpretado por Fábio Cury con acompañamiento en el piano de Alessandro Santoro. Las actividades musicales de Fábio Cury se han destacado principalmente por su eclecticismo: van desde el área de música orquestal hasta el mundo académico, desde
Cury, Fábio - Fagot (Brasil)
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Genetic Variation in ADHD‐Related Risk Genes in an Indigenous Population of the Amazon
ABSTRACT Attention‐Deficit/Hyperactivity Disorder (ADHD) is a highly heritable neurodevelopmental disorder; however, its genetic architecture remains poorly explored in Indigenous populations. This study aimed to analyze and characterize genetic variation in 11 genes (ADGRL3, CDH8, DCC, DUSP6, FOXP1, FOXP2, MEF2C, PCDH7, SEMA6D, SORCS3, and ST3GAL3 ...
Hirlesson Paixão de Matos +11 more
wiley +1 more source
CIRURGIA DE ALTEMEIER: UMA BOA OPÇÃO DE TRATAMENTO PARA PROCIDÊNCIA RETAL
Priscilla Martins +6 more
doaj +1 more source

