FABIOLA JUSTE

(Fonte: Lattes)
Índice h a partir de 2011
7
Projetos de Pesquisa
Unidades Organizacionais
Departamento de Fisioterapia, Fonoaudiologia e Terapia Ocupacional, Faculdade de Medicina
LIM/34 - Laboratório de Ciências da Reabilitação, Hospital das Clínicas, Faculdade de Medicina

Resultados de Busca

Agora exibindo 1 - 3 de 3
  • article
    Aspectos da fluência da fala em crianças com distúrbio específico de linguagem
    (2014) ANDRADE, Cláudia Regina Furquim de; BEFI-LOPES, Debora Maria; JUSTE, Fabíola Staróbole; CÁCERES-ASSENÇO, Ana Manhani; FORTUNATO-TAVARES, Talita Maria
    Purpose The present study aimed to assess specific aspects of speech fluency in children with specific language impairment (SLI). This included examining the typology of speech disruption and rate (in words and syllables per minute), across different age groups. Methods A total of 50 children, aged 3 to 7 years old, presenting with nonverbal IQ and hearing thresholds within normal limits (without the presence of stuttering) participated in the study. Children were divided into two groups: G1 (SLI) included 25 children (7 girls and 18 boys) and G2 (typical development) included 25 children matched on age and gender with G1. Each child was shown a figure and asked to discuss what s/he liked about the figure. Each speech sample included 200 fluent syllables or 100 fluent words. Results Between-group analyses demonstrated that children aged 3 to 4 years old in G1 had lower speech rate than their age-matched peers from G2. Within-group analyses revealed no differences in disruption typologies between age groups in G1 participants. In contrast, hesitation was the most frequent typology for 4- to 5-year-old G2 children, whereas hesitation and word repetition typologies were observed in 6- to 7-year-old G2 children. Conclusion Children with suspected SLI between the ages of 3 to 4 years old showed a reduction in word and syllable production. Hesitation-type speech disruptions were prominently used by typically developing children, regardless of age, and were not observed in SLI children.
  • article 2 Citação(ões) na Scopus
    Self-perception of people who stutter regarding their experiences and results of stuttering treatments
    (2014) ANDRADE, Claudia Regina Furquim de; CUNHA, Maria Claudia; JUSTE, Fabiola Staróbole; RITTO, Ana Paula; ALMEIDA, Beatriz Paiva Bueno de
    Purpose: To investigate the opinion about stuttering treatments in people who stutter, based on their answers to two open questions. Methods: The participants were 40 adults of both genders, with self-reported stuttering. During the first phase of the research, we contacted two Brazilian nongovernmental organizations: the Brazilian Stuttering Association (ABRAGAGUEIRA) and the Brazilian Fluency Institute (IBF). These associations agreed to participate and were responsible for sending the research questions to their members via electronic mail. The first contact with the participants elucidated the purpose and method of our research and, after obtaining informed consent from participants, the two questions were sent. The research questions involved their opinion about cure, treatments to which the participants had been submitted, and their outcome. Results: After analysis, the answers obtained indicated that people who stutter believe in a cure for stuttering; that the ideal therapy would be the one that led to the disappearance of the symptoms; and the most frequently reported professional to treat the disorder is the speech-language pathologist. The results also indicated that although most of the participants had undergone speech-language treatment for stuttering, neither significant improvements were observed nor satisfaction was positive. Conclusion: The results indicate that the answers presented by the participants were not based on scientific knowledge about the disorder but on their wish that ""something could happen"" to make stuttering ""disappear."" Although in this study we did not investigate the type of treatment to which the patients were submitted, the results suggest that the factors that contribute to an effective treatment are contentious.
  • article 10 Citação(ões) na Scopus
    A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10
    (2014) DOMINGUES, C. E. F.; OLIVERA, C. M. C.; OLIVEIRA, B. V.; JUSTE, F. S.; ANDRADE, C. R. F.; GIACHETI, C. M.; MORETTI-FERREIRA, D.; DRAYNA, D.
    Although twin, adoption, and family studies demonstrate that genetic factors are involved in the origins of stuttering, the mode of transmission of the disorder in families is not well defined and stuttering is considered a genetically complex trait. We performed a genome-wide linkage scan in a group of 43 Brazilian families, each containing multiple cases of persistent developmental stuttering. Linkage analysis under a dominant model of inheritance generated significant evidence of linkage in two Brazilian families, with a combined maximum single-point LOD score of 4.02 and a multipoint LOD score of 4.28 on chromosome 10q21. This demonstrated the presence of a novel variant gene at this locus that predisposes individuals to stuttering, which provides an opportunity to identify novel genetic mechanisms that underlie this disorder.