UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Molecular screening of patients with profound hearing loss from Chengdu, China

Acta oto-laryngologica, 2022, Vol.142 (1), p.57-60

2022

Volltextzugriff (PDF)

The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in Austria

Acta oto-laryngologica, 2017-04, Vol.137 (4), p.356-360

2017

Volltextzugriff (PDF)

Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China

Acta oto-laryngologica, 2015-06, Vol.135 (6), p.586-591

2015

Volltextzugriff (PDF)

Is deafness etiology important for prediction of functional outcomes in pediatric cochlear implantation?

Acta oto-laryngologica, 2014-06, Vol.134 (6), p.571-578

2014

Volltextzugriff (PDF)

Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)

Acta oto-laryngologica, 2012-04, Vol.132 (4), p.377-384

2012

Volltextzugriff (PDF)

Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants

Acta oto-laryngologica, 2014-04, Vol.134 (4), p.373-381

2014

Volltextzugriff (PDF)

Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord

Acta oto-laryngologica, 2011-09, Vol.131 (9), p.976-982

2011

Volltextzugriff (PDF)

Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China

Acta oto-laryngologica, 2014-09, Vol.134 (9), p.924-929

2014

Volltextzugriff (PDF)

The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature review

Acta oto-laryngologica, 2015-09, Vol.135 (9), p.914-918

2015

Volltextzugriff (PDF)

Outcome of cochlear implantation in children with congenital cytomegalovirus infection or GJB2 mutation

Acta oto-laryngologica, 2012-06, Vol.132 (6), p.597-602

2012

Volltextzugriff (PDF)

Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China

Acta oto-laryngologica, 2013-09, Vol.133 (9), p.930-934

2013

Volltextzugriff (PDF)

Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss

Acta oto-laryngologica, 2013-08, Vol.133 (8), p.833-841

2013

Volltextzugriff (PDF)

GJB2 (Connexin 26) gene mutations among hearing-impaired persons in a Swedish cohort

Acta oto-laryngologica, 2012-12, Vol.132 (12), p.1301-1305

2012

Volltextzugriff (PDF)

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

Acta oto-laryngologica, 2011-02, Vol.131 (2), p.124-129

2011

Volltextzugriff (PDF)

Vestibular function of patients with profound deafness related to GJB2 mutation

Acta oto-laryngologica, 2010-09, Vol.130 (9), p.990-995

2010

Volltextzugriff (PDF)

Three common GJB2 mutations causing nonsyndromic hearing loss in Chinese populations are retained in the endoplasmic reticulum

Acta oto-laryngologica, 2010-07, Vol.130 (7), p.799-803

2010

Volltextzugriff (PDF)

Identification of a p.R143Q dominant mutation in the gap junction beta-2 gene in three Chinese patients with different hearing phenotypes

Acta oto-laryngologica, 2012, Vol.133 (1), p.55-58

2012

Volltextzugriff (PDF)

Impaired membrane targeting and aberrant cellular localization of human Cx26 mutants associated with inherited recessive hearing loss

Acta oto-laryngologica, 2011-01, Vol.131 (1), p.59-66

2011

Volltextzugriff (PDF)

Homozygous M34T mutation of the GJB2 gene associates with an autosomal recessive nonsyndromic sensorineural hearing impairment in Finnish families

Acta oto-laryngologica, 2012-08, Vol.132 (8), p.862-873

2012

Volltextzugriff (PDF)

Performance of speech perception after cochlear implantation in DFNB1 patients

Acta oto-laryngologica, 2009-01, Vol.129 (4), p.395-398

2009

Volltextzugriff (PDF)

Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations

Acta oto-laryngologica, 2011-11, Vol.131 (11), p.1232-1236

2011

Volltextzugriff (PDF)

Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation

Acta oto-laryngologica, 2011-09, Vol.131 (9), p.970-975

2011

Volltextzugriff (PDF)

Expression of the gap junction proteins connexin 26 and connexin 43 in human middle ear cholesteatoma

Acta oto-laryngologica, 2006-02, Vol.126 (2), p.138-143

2006

Volltextzugriff (PDF)

Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele

Acta oto-laryngologica, 2004-05, Vol.124 (552), p.29-34

2004

Volltextzugriff (PDF)

The responsible genes in Japanese deafness patients and clinical application using Invader assay

Acta oto-laryngologica, 2008-01, Vol.128 (4), p.446-454

2008

Volltextzugriff (PDF)

1 – 25 von 30

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieActa Oto-Laryngologica

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(30)
Mit Volltextzugriff
(30)

Publikationsform

Artikel
(30)

Sprache

Englisch
(30)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(30)
Otorhinolaryngology
(30)
Science & Technology
(30)
Connexin 26
(29)
Humans
(28)
Connexins - Genetics
(26)
Female
(20)
Male
(20)
Biological And Medical Sciences
(17)
Child
(16)
Medical Sciences
(16)
Otorhinolaryngology. Stomatology
(16)
Adult
(15)
Child, Preschool
(14)
Ear, Auditive Nerve, Cochleovestibular Tract, Facial Nerve: Diseases, Semeiology
(14)
Dna Mutational Analysis
(13)
Non Tumoral Diseases
(13)
Young Adult
(12)
Adolescent
(11)
Deafness - Genetics
(11)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

1 weiteren anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Acta Oto-Laryngologica. Supplement
(2)

Menü

Weitere Dienste

Einstellungen

Molecular screening of patients with profound hearing loss from Chengdu, China

The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in Austria

Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China

Is deafness etiology important for prediction of functional outcomes in pediatric cochlear implantation?

Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)

Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants

Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord

Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China

The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature review

Outcome of cochlear implantation in children with congenital cytomegalovirus infection or GJB2 mutation

Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China

Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss

GJB2 (Connexin 26) gene mutations among hearing-impaired persons in a Swedish cohort

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

Vestibular function of patients with profound deafness related to GJB2 mutation

Three common GJB2 mutations causing nonsyndromic hearing loss in Chinese populations are retained in the endoplasmic reticulum

Identification of a p.R143Q dominant mutation in the gap junction beta-2 gene in three Chinese patients with different hearing phenotypes

Impaired membrane targeting and aberrant cellular localization of human Cx26 mutants associated with inherited recessive hearing loss

Homozygous M34T mutation of the GJB2 gene associates with an autosomal recessive nonsyndromic sensorineural hearing impairment in Finnish families

Performance of speech perception after cochlear implantation in DFNB1 patients

Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations

Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation

Expression of the gap junction proteins connexin 26 and connexin 43 in human middle ear cholesteatoma

Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele

The responsible genes in Japanese deafness patients and clinical application using Invader assay

Aktive Filter

Suchergebnisse filtern