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Mostrando ítems 61-70 de 93
Deficiência auditiva referida em inquérito de saúde no município de Botucatu, ISA-SP, 2001-02
(Universidade Estadual Paulista (Unesp), 2007-05-07)
Estimar a prevalência de deficiência auditiva na população urbana de Botucatu-SP e analisar as condições de vida e uso dos serviços de saúde das pessoas que relataram tal agravo. Análise do banco de dados pertencente ao ...
Associação entre otalgia, zumbido, vertigem e hipoacusia com desordens temporomandibulares
(2009-01-01)
Because nonespecific symptoms and signs are associated with others well-established in the temporomandibular disorders, it is difficult for the clinician to decide what symptoms and signs should be considered during the ...
Associação entre otalgia, zumbido, vertigem e hipoacusia com desordens temporomandibulares
(2009-01-01)
Because nonespecific symptoms and signs are associated with others well-established in the temporomandibular disorders, it is difficult for the clinician to decide what symptoms and signs should be considered during the ...
Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss
(Elsevier MassonIssy les Moulineaux, 2014-03)
In 20% of cases, hereditary non-syndromic hearing loss has an autosomal dominant inheritance (ADNSHL). To date, more than 50 loci for ADNSHL have been mapped to different chromosomal regions. In order to verify whether ...
Autism associated to a deficiency of complexes III and IV of the mitochondrial respiratory chain.
(Universidad del Zulia, 2013)
Chromosome imbalances in syndromic hearing loss
(WILEY-BLACKWELL PUBLISHING, INC, 2009)
The cause of hearing impairment has not been elucidated in a large proportion of patients. We screened by 1-Mb array-based comparative genomic hybridization (aCGH) 29 individuals with syndromic hearing impairment whose ...
Deficiência auditiva referida em inquérito de saúde no município de Botucatu, ISA-SP, 2001-02
(Universidade Estadual Paulista (UNESP), 2014)