Neurodevelopment
Mostrando 25-36 de 38 artigos, teses e dissertações.
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25. Avaliação nutricional antropometrica de crianças com paralisia cerebral / Anthropometric status in children with cerebral palsy
Cerebral Palsy (CP) is a wide term, it includes a group of nonprogressive, but usually mutable, motor disorders which mean the effects of early cerebral injuries or malformation occurred in child neurodevelopment. Malnutrition is frequent in children with CP. Present research studied nutritional status in 114 children (2 to 12.9 years) with CP, from the gast
Publicado em: 2006
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26. Estudo de associação entre Síndrome de Tourette e genes da via Slit-Robo
Tourette syndrome (TS) is a neuropsichyatric disorder characterized by tics and familiar inheritance. Several research groups are investigating the genetic aspects of TS, however, frequently the findings are not replicated in subsequent studies. Study of gene Slit and trk-like family member 1 (SLITRK1) has shown correlation with TS in three non-related patie
Publicado em: 2006
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27. Evolução neurologica de recem-nascidos com asfixia neonatal
The aim of this study was to evaluate the neurological examination and neurodevelopment by Denver Development Screening Test (DDST) evolution, at one year and its association with clinical variables, in 81 term neonates with birth asphyxia, born in the Maternity Unit of the Center for Integral Assistance to Women?s Health at the State University of Campinas,
Publicado em: 2005
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28. Neurodevelopmental risk factors in schizophrenia
The authors review environmental and neurodevelopmental risk factors for schizophrenic disorders, with emphasis on minor physical anomalies, particularly craniofacial anomalies and dermatoglyphic variations. The high prevalence of these anomalies among schizophrenic subjects supports the neurodevelopmental theory of the etiology of schizophrenia, since they
Brazilian Journal of Medical and Biological Research. Publicado em: 2001-02
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29. Tetraploidy in a liveborn infant.
We report a 3 month old boy with tetraploidy, found in peripheral blood and skin fibroblast cultures, with severely delayed growth and neurodevelopment, and with a cleft lip; these findings have not been described before. This report brings to seven the total number of liveborn infants with a 92,XXYY karyotype.
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30. To sleep, perchance to enrich learning?
There is evidence that sleep enhances memory and learning. Childhood is a critical period for neurodevelopment, and minor but persistent disruption of sleep may have long‐term implications for cognitive performance. Sleep is critical for health and is undervalued both in our 24 h society and in paediatric clinical practice. Paediatricians need to underst
BMJ Group.
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31. A randomised multicentre study of human milk versus formula and later development in preterm infants.
Whether breast milk influences later neurodevelopment has been explored in non-randomised studies, potentially confounded by social and demographic differences between feed groups. Here in a strictly randomised prospective multicentre trial, Bayley psychomotor and mental development indices (PDI and MDI) were assessed at 18 months postterm in survivors of 50
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32. Cerebellin: a quantifiable marker for Purkinje cell maturation.
The cerebellum-specific hexadecapeptide cerebellin has been localized by immunocytochemical means to the perikarya and dendrites of cerebellar Purkinje cells. Biochemical analysis using ion-pairing HPLC shows cerebellin to first appear 5 days after birth, whereafter levels rise to a maximum at 25 days postpartum, and then decline to stable adult values. This
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33. Neonatal nasal intermittent positive pressure ventilation: what do we know in 2007?
Although neonatal nasal intermittent positive pressure ventilation (NIPPV) is widely used today, its place in neonatal respiratory support is yet to be fully defined. Current evidence indicates that NIPPV after extubation of very premature infants reduces the rate of reintubation. However, much is still not known about NIPPV including its mechanisms of actio
BMJ Group.
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34. Reelin molecules assemble together to form a large protein complex, which is inhibited by the function-blocking CR-50 antibody
Reelin is a key mediator of ordered neuronal alignment in the brain. Here, we demonstrate that Reelin molecules assemble with each other to form a huge protein complex both in vitro and in vivo. The Reelin–Reelin interaction clearly is inhibited by the function-blocking anti-Reelin antibody, CR-50, at a concentration known to inhibit Reelin function. This
The National Academy of Sciences.
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35. A Quantitative ELISA Assay for the Fragile X Mental Retardation 1 Protein
Non-coding (CGG-repeat) expansions in the fragile X mental retardation 1 (FMR1) gene result in a spectrum of disorders involving altered neurodevelopment (fragile X syndrome), neurodegeneration (late-onset fragile X-associated tremor/ataxia syndrome), or primary ovarian insufficiency. While reliable and quantitative assays for the number of CGG repeats and F
American Society for Investigative Pathology.
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36. The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome
Triple A syndrome is a human autosomal recessive disorder characterized by an unusual array of tissue-specific defects. Triple A syndrome arises from mutations in a WD-repeat protein of unknown function called ALADIN (also termed Adracalin or AAAS). We showed previously that ALADIN localizes to nuclear pore complexes (NPCs), large multiprotein assemblies tha
The National Academy of Sciences.