Robin Sequence
Mostrando 1-12 de 19 artigos, teses e dissertações.
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1. Intensive treatment of speech disorders in robin sequence: a case report
ABSTRACT Purpose To describe the speech of a patient with Pierre Robin Sequence (PRS) and severe speech disorders before and after participating in an Intensive Speech Therapy Program (ISTP). Methods The ISTP consisted of two daily sessions of therapy over a 36-week period, resulting in a total of 360 therapy sessions. The sessions included the phases of e
CoDAS. Publicado em: 23/10/2017
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2. Disgenesias dentárias na síndrome Richieri-Costa-Pereira / Tooth abnormalities in the Richieri-Costa-Pereira syndrome
Objetivo: Investigar a prevalência de disgenesias dentárias em indivíduos com síndrome Richieri-Costa-Pereira. Material e Métodos: 13 indivíduos, registrados no Hospital de Reabilitação de Anomalias Craniofaciais - Universidade de São Paulo (HRAC-USP), Bauru Brasil, com síndrome Richieri-Costa-Pereira, de ambos os gêneros, de etnia branca, acima d
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 05/12/2011
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3. Nasalidade de crianças com sequência de Robin após palatoplastia primária com as técnicas de Furlow ou von Langenbeck / Nasality in children with Robin sequence after primary palatoplasty with Furlow or von Langenbeck procedures
Objetivo: O objetivo deste estudo foi comparar nasalidade de fala em crianças com sequência de Robin isolada, operadas pela técnica de palatoplastia de Furlow, com a fala de crianças operadas pela técnica de von Langenbeck. Modelo: Estudo prospectivo. Local de execução: Setor de Fonoaudiologia e Laboratório de Fonética do Hospital de Reabilitação
Publicado em: 2009
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4. Assessment of self-care capacity of infant caretakers with Robin Sequence / Avaliação da capacidade de cuidadores de lactentes com Seqüência de Robin
Objetivos: Utilizando-se o referencial Teórico do autocuidado de Dorothea Orem o estudo tem como objetivo: avaliar a capacidade de autocuidado do agente de autocuidado (AAC) de lactentes com Seqüência de Robin isolada (SRI), quanto à manipulação e o tempo que o AAC levou para adquirir a capacidade de cuidados com a intubação nasofaríngea (INF); sond
Publicado em: 2008
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5. Perfil das crianças portadoras de disfagia orofaríngea associada às anomalias craniofaciais internadas no HRAC-USP / Profile of children with oropharyngeal dysphagia related to craniofacial deformities interned at HRAC-USP
Objective: To draw up guidelines for the treatment. Model: Retrospective analysis of historical of 236 children, during the period July 2003 to July 2006 and descriptive analysis of the results. Environment: Special Care Unit by HRAC-USP. Participants: 236 children with oropharyngeal dysphagia, aged 3 days to 8 years, 204 (86.4%) had cleft lip, and / or pala
Publicado em: 2008
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6. Audiologic triage in neonates with Robin sequence / Triagem audiológica em lactentes com seqüência de Robin
Objectives: To investigate the occurency of hearin problems in children with Robin Sequence (RS) aged 1 to 3 years old with cleft palate not submitted to palatoplasty. To compare the frequency of hearing problems in children with RS only (group 1), children with other anomalies associated to RS (group 2), at the some age, not submitted to palatoplasty. Resul
Publicado em: 2004
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7. Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2
BMJ Group.
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8. DNA Sequence Variation within vanA, vanB, vanC-1, and vanC-2/3 Genes of Clinical Enterococcus Isolates
We studied the DNA sequence variation of van genes of 34 isolates of Enterococcus spp. The isolates containing the vanB gene exhibited between 0 and 41 base pair changes per 801 bp studied when the vanB sequences were compared to that of the reference strain Enterococcus faecalis V583. The isolates carrying the vanC-2 gene exhibited between 0 and 23 base pai
American Society for Microbiology.
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9. The Biopesticide Paenibacillus popilliae Has a Vancomycin Resistance Gene Cluster Homologous to the Enterococcal VanA Vancomycin Resistance Gene Cluster
We have previously identified, in Paenibacillus popilliae, a 708-bp sequence which has homology to the sequence of the enterococcal vanA gene. We have performed further studies revealing five genes encoding homologues of VanY, VanZ, VanH, VanA, and VanX in P. popilliae. The predicted amino acid sequences are similar to those in VanA vancomycin-resistant ente
American Society for Microbiology.
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10. Induction of Host Gene Expression following Infection of Chicken Embryo Fibroblasts with Oncogenic Marek's Disease Virus
Microarrays containing 1,126 nonredundant cDNAs selected from a chicken activated T-cell expressed sequence tag database (http://chickest.udel.edu) were used to examine changes in host cell gene expression that accompany infection of chicken embryo fibroblasts (CEF) with Marek's disease virus (MDV). Host genes that were reproducibly induced by infection of C
American Society for Microbiology.
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11. The complete genome sequence of the Arabidopsis and tomato pathogen Pseudomonas syringae pv. tomato DC3000
We report the complete genome sequence of the model bacterial pathogen Pseudomonas syringae pathovar tomato DC3000 (DC3000), which is pathogenic on tomato and Arabidopsis thaliana. The DC3000 genome (6.5 megabases) contains a circular chromosome and two plasmids, which collectively encode 5,763 ORFs. We identified 298 established and putative virulence
National Academy of Sciences.
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12. PCR assay confirms diagnosis in syndrome with variably expressed phenotype: mutation detection in Stickler syndrome.
Stickler syndrome is an autosomal dominant disease with ocular (severe myopia, vitreal degeneration, and retinal detachment) and other systemic manifestations (hearing loss, cleft palate, epiphyseal dysplasia, and premature osteoarthritis). As with other dominantly inherited conditions, the clinical phenotype of Stickler syndrome varies considerably. To date