Biblioteca
Virtual em Saúde
224
[X ring chromosome]
29
[Hypoacusis-deafness related to perinatal adverse conditions.
According to the register available in a specialized unit of
Ciudad de Mexico. Analysis according to birth weight]
30
Hipoacusia-sordera asociada a condiciones perinatales adversas
según registro en unidad especializada de la ciudad de
México. Análisis en función del peso al
nacimiento/ Hypoacusis-deafness related to perinatal adverse
conditions. According to the register available in a specialized
unit of ciudad de Mexico. Analysis according to birth weight
31
'Some aspects of cognitive and social development in children
with cochlear implant'.
36
Deafness, culture, and choice.
39
Electronystagmography in a patient with a sudden unilateral
sensorineural hearing loss.
41
[Congenital rubella syndrome developing after a 1987-1988 epidemic
in Japan]
46
Obstetric handling of a deaf patient.
47
Is there a coherent social conception of disability?
48
Otological evaluation of newborns who failed otoacoustic emission
screening.
53
[Hyperbaric oxygen therapy (indications and uses)]
56
Partial and double-array implantation of the ossified cochlea.
65
Oto-palato-digital syndrome with features of type I and II in
brothers.
86
Síndrome da rubéola congênita relacionada
ao período gestacional de aquisiçäo da doença:
características audiológicas/ Congenital rubella
syndrome related to the period of onset of the disease during
pregnancy: audiological findings
87
Safety issues in magnetic resonance imaging.
106
Toxoplasmosis: maternal and pediatric findings in 23,000 pregnancies.
107
Previously undescribed syndrome of craniofacial, hand anomalies,
and sensorineural deafness.
115
Relationship of growth and psychoneurologic status of 2-year-old
children of birthweight 500-999 g.
118
Histopathologic and experimental models for sensory and neural
deafness.
130
Intrauterinely acquired Pseudomonas infection in the neonate.
131
A prospective study of children [quot ]at risk[quot ] for deafness.
132
In search of the aetiology of deafness in Nigeria--the probable
role of rubella infection.
133
[Rubella deafness. Audiometric, ophthalmologic, epidemiological
aspects]
134
Retrospective rubella review, Maldives.
135
Analysis of a cohort of children with sensory hearing loss using
the SCALE systematic nomenclature.
138
Cytomegalovirus reactivation in pregnancy and subsequent isolated
bilateral hearing loss in the infant.
145
Molecular basis of congenital and acquired deafness.
146
[Early diagnosis of childhood deafness: detection protocol in
high-risk neonates]
147
Diagnóstico precoz de hipoacusia infantil: protocolo
de detección en neonatos de alto riesgo/ Early diagnosis
of childhood deafness: detection protocol in high-risk neonates
148
'Glue ear' in perspective.
149
Variation in the vitreous phenotype of Stickler syndrome can
be caused by different amino acid substitutionsin the X position
of the type II collagen Gly-X-Y triple helix.
150
Deafblindness: living with sensory deprivation.
151
Global problem of drug-induced hearing loss.
152
Probably Norrie's disease due to mutation. Two sporadic sibships
of two males each, a necropsy of one case, and, given Norrie's
disease, a calculation of the gene mutation frequency.
153
Potential pitfalls of initiating a newborn hearing screening
program.
154
Health status of a population of infants born before 26 weeks
gestation derived from routine data collected between 21 and
27 months post-delivery.
155
Preference for infant-directed singing in 2-day-old hearing
infants of deaf parents.
156
A stepwise approach to the diagnosis and treatment of hereditary
hearing loss.
157
Amplification for infants: selection and verification.
158
Genetics and molecular biology of deafness.
159
Preconditions of language development in deaf children.
160
Two cases of Townes-Brocks syndrome.
161
Lullabies for Sophia.
162
Feingold syndrome--a cause of profound deafness.
163
Premature cataracts associated with generalized lentigo.
164
The need for universal neonatal hearing screening--some aspects
of epidemiology and identification.
165
Automated auditory brainstem response in neonatal hearing screening.
166
Controlled trial of universal neonatal screening for early identification
of permanent childhood hearing impairment: coverage, positive
predictive value, effect on mothers and incremental yield. Wessex
Universal Neonatal Screening Trial Group.
167
[Quality control of an early detection, diagnosis and early
intervention program for deafness in newborn. Official document
of the Early Detection Comission of Deafness in Newborn (CODEPEH)]
168
Control de calidad de un programa de detección, diagnóstico
e intervención precoz de la hipoacusia en recién
nacidos. Documento oficial de la comisión para la Detección
de la Hipoacusia en Recién Nacidos (CODEPEH)/ Quality
control of an early detection, diagnosis and early intervention
program for deafness in newborn. Official document of the Early
Detection Comission of Deafness in Newborn (CODEPEH)
169
Genetic causes of goiter and deafness: Pendred syndrome in a
girl and cooccurrence of Pendred syndrome and resistance to
thyroid hormone in her sister.
