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Prelingual Deafness
Known as:
Deafness, Prelingual
National Institutes of Health
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Related topics
Related topics
1 relation
Deaf Mutism
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects
Yufen Guo
,
Xiao-wen Liu
,
+5 authors
Qiuju Wang
Acta Oto-Laryngologica
2008
Corpus ID: 28096922
Conclusion. This genetic epidemiological study demonstrated that 26.65% of the prelingual deafness in Northern Chinese patients…
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2007
2007
Prevalence of prelingual deafness in Italy.
L. Bubbico
,
A. Rosano
,
A. Spagnolo
Acta otorhinolaryngologica italica
2007
Corpus ID: 18737684
Neonatal hearing loss is the most frequent sensorial congenital defect in newborns. No data are available on worldwide prevalence…
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Highly Cited
2003
Highly Cited
2003
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey
Mustafa Tekin
,
T. Duman
,
+6 authors
Nejat Akar
European Journal of Pediatrics
2003
Corpus ID: 2999286
Considerable differences on the frequencies of the mitochondrial 12S rRNA A1555G and tRNASer(UCN) A7445G mutations have been…
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Highly Cited
2003
Highly Cited
2003
Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness
H. Hwa
,
T. Ko
,
+5 authors
Chia-Kai Hsu
Genetics in Medicine
2003
Corpus ID: 36827005
Purpose: To determine the mutation spectrum of the connexin 26 gene among 324 Taiwanese patients with prelingual deafness and the…
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Highly Cited
2002
Highly Cited
2002
Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East
Hashem Shahin
,
T. Walsh
,
+4 authors
Moien Kanaan
Human Genetics
2002
Corpus ID: 15202450
Abstract. In some Palestinian communities, the prevalence of inherited prelingual deafness is among the highest in the world. As…
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Highly Cited
2002
Highly Cited
2002
Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan
Yi-Chun Wang
,
Chiu-Yun Kung
,
+5 authors
Shuan-yow Li
European Journal of Human Genetics
2002
Corpus ID: 1644733
Mutations in the Cx26 (GJB2) gene have been shown to be responsible for a major part of autosomal recessive non-syndromic…
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Highly Cited
2000
Highly Cited
2000
Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.
Takayuki Kudo
,
K. Ikeda
,
+6 authors
T. Takasaka
American journal of medical genetics
2000
Corpus ID: 1188066
Mutations in the connexin 26 gene (GJB2), which encodes a gap-junction protein and is expressed in the inner ear, have been shown…
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Highly Cited
2000
Highly Cited
2000
Syntactic and Semantic Processing in Hebrew Readers with Prelingual Deafness
P. Miller
American Annals of the Deaf
2000
Corpus ID: 10802051
The experimenter investigated the effect of semantic clues on the reading comprehension of deaf and hearing Israeli children. Two…
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Highly Cited
1997
Highly Cited
1997
Speech perception skills and speech production intelligibility in French children with prelingual deafness and cochlear implants.
M. Mondain
,
M. Sillon
,
+4 authors
A. Uziel
Archives of Otolaryngology - Head and Neck…
1997
Corpus ID: 36371994
OBJECTIVE To examine speech perception and production intelligibility in French children with prelingual deafness who received…
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Highly Cited
1994
Highly Cited
1994
Results of multichannel cochlear implants in congenital and acquired prelingual deafness in children: five-year follow-up.
B. Gantz
,
R. Tyler
,
G. Woodworth
,
N. Tye‐Murray
,
H. Fryauf-Bertschy
American Journal of Otology
1994
Corpus ID: 26756767
Postlingually deafened children, using multichannel cochlear implants, have achieved substantial improvement in their speech…
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