Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Nayara Thais de Oliveira Costa"'
Publikováno v:
International Archives of Otorhinolaryngology, Vol 17, Iss 04, Pp 395-402 (2013)
Abstract Introduction For infants under 6 months, the literature recommends 1,000-Hz tympanometry, which has a greater sensitivity for the correct identification of middle ear disorders in this population. Objective To systematically analyze nati
Externí odkaz:
https://doaj.org/article/e368cb7e8675490383278014a9c77e65
Publikováno v:
International Archives of Otorhinolaryngology v.17 n.4 2013
International Archives of Otorhinolaryngology
Fundação Otorrinolaringologia (FORL)
instacron:FORL
International Archives of Otorhinolaryngology, Vol 17, Iss 04, Pp 395-402 (2013)
International Archives of Otorhinolaryngology, Volume: 17, Issue: 4, Pages: 395-402, Published: 2013
International Archives of Otorhinolaryngology
Fundação Otorrinolaringologia (FORL)
instacron:FORL
International Archives of Otorhinolaryngology, Vol 17, Iss 04, Pp 395-402 (2013)
International Archives of Otorhinolaryngology, Volume: 17, Issue: 4, Pages: 395-402, Published: 2013
Introduction For infants under 6 months, the literature recommends 1,000-Hz tympanometry, which has a greater sensitivity for the correct identification of middle ear disorders in this population. Objective To systematically analyze national and inte
Autor:
Ana Claudia Martinho-Carvalho, Nayara Thais de Oliveira Costa, Maria Claudia Cunha, Doris Ruthi Lewis
Publikováno v:
Jornal da Sociedade Brasileira de Fonoaudiologia v.24 n.2 2012
Jornal da Sociedade Brasileira de Fonoaudiologia
Sociedade Brasileira de Fonoaudiologia (SBF)
instacron:SBF
Jornal da Sociedade Brasileira de Fonoaudiologia, Volume: 24, Issue: 2, Pages: 181-187, Published: 2012
Jornal da Sociedade Brasileira de Fonoaudiologia
Sociedade Brasileira de Fonoaudiologia (SBF)
instacron:SBF
Jornal da Sociedade Brasileira de Fonoaudiologia, Volume: 24, Issue: 2, Pages: 181-187, Published: 2012
This study had the aim to investigate the auditory and communicative abilities of children diagnosed with Auditory Neuropathy Spectrum Disorder due to mutation in the Otoferlin gene. It is a descriptive and qualitative study in which two siblings wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccfb3ac032d63bd1dbac0a92ca2d1f15
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2179-64912012000200016
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2179-64912012000200016