_________Biblioteca
Virtual em Saúde___________
5
mouse model for nonsyndromic deafness (DFNB12) links hearing
loss to defects in tip links of mechanosensory hair cells.
6
Elucidation of separate, but collaborative functions of the
rRNA methyltransferase-related human mitochondrial transcription
factors B1 and B2 in mitochondrial biogenesis reveals new insight
into maternally inherited deafness.
7
GRM7 variants confer susceptibility to age-related hearing impairment.
15
Tone deafness: a new disconnection syndrome?
21
Morphology of the insula in relation to hearing status and sign
language experience.
22
Digenic inheritance of non-syndromic deafness caused by mutations
at the gap junction proteins Cx26 and Cx31.
24
The effect of long-term unilateral deafness on the activation
pattern in the auditory cortices of French-native speakers:
influence of deafness side.
32
Word recognition following implantation of conventional and
10-mm hybrid electrodes.
42
Método para medida do comprimento da cóclea por
meio de ressonância magnética/ A method for measuring
the length of the coclea through magnetic resonance imaging
45
TRPML3 mutations cause impaired mechano-electrical transduction
and depolarization by an inward-rectifier cation current in
auditory hair cells of varitint-waddler mice.
49
Cortical circuits for silent speechreading in deaf and hearing
people.
57
Effects of age at onset of deafness and electrical stimulation
on the developing cochlear nucleus in cats.
58
Effects of deafening and cochlear implantation procedures on
postimplantation psychophysical electrical detection thresholds.
60
Processing F0 with cochlear implants: Modulation frequency discrimination
and speech intonation recognition.
63
Using early language outcomes to predict later language ability
in children with cochlear implants.
66
Relational learning in children with deafness and cochlear implants.
68
Effect of instrument timbre on melodic contour identification
by cochlear implant users.
96
Deafness and visual enumeration: not all aspects of attention
are modified by deafness.
108
[Descriptive cross-sectional study of hearing-disabled children
at the National Institute for Education of the Deaf in Rio de
Janeiro, Brazil.]
118
Efeitos do potencial de ação neural sobre a percepção
de fala em usuários de implante coclear/ Influence of
evoked compound action potential on speech perception in cochlear
implant users
127
[Effect of sound amplification on parent's communicative modalities]
196
Brainstem auditory evoked response (BAER) testing in animals.
200
A investigação genética na surdez hereditária
não-sindrômica/ Genetic investigation of non-syndromic
hereditary deafness
203
Potencial cognitivo P300 realizado em campo livre: aplicabilidade
do teste/ P300 cognitive potencial in free field: applicability
test
204
Targeted disruption of the Kvlqt1 gene causes deafness and gastric
hyperplasia in mice.
206
Cadherin 23 and protocadherin 15 interact to form tip-link filaments
in sensory hair cells.
210
In vitro 3'-end endonucleolytic processing defect in a human
mitochondrial tRNA(Ser(UCN)) precursor with the U7445C substitution,
which causes non-syndromic deafness.
214
[Reproductive autonomy: a case study on deafness]
215
Oscillucusis and sudden deafness in a migraine patient
216
Treponema pallidum y la sordera de Ludwig van Beethoven/ Treponema
pallidum and Ludwig van Beethoven's deafness
218
Sindrome de Waardenburg: achados audiológicos em 2 irmãos/
Waardenburg's syndrome: audiological findings in 2 brothers
219
Perda auditiva genética/ Genetic hearing loss
77
Self-rated mental health, school adjustment, and substance use
in hard-of-hearing adolescents.
