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Ana Rakita et al.
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Bong Jik Kim et al.
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Erika Woodson et al.
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Angel Ramos-Macias et al.
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Jourdan T. Holder et al.
OTOLOGY & NEUROTOLOGY (2019)
Initial surgical and clinical experience with the Nucleus C1532 slim modiolar electrode in the UK
Manuel Gomez Serrano et al.
COCHLEAR IMPLANTS INTERNATIONAL (2019)
Long-Term Outcomes of Cochlear Implantation in Patients With High-Frequency Hearing Loss
J. Thomas Roland et al.
LARYNGOSCOPE (2018)
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Hela Azaiez et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss
Andrea M. Oza et al.
HUMAN MUTATION (2018)
Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss
Rongrong Wang et al.
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Electrode Location and Audiologic Performance After Cochlear Implantation: A Comparative Study Between Nucleus CI422 and CI512 Electrode Arrays
Brendan P. O'Connell et al.
OTOLOGY & NEUROTOLOGY (2016)
Novel Mutations in LRTOMT Associated With Moderate Progressive Hearing Loss in Autosomal Recessive Inheritance
Aya Ichinose et al.
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Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population
Nayoung K. D. Kim et al.
GENETICS IN MEDICINE (2015)
Effects of steep high-frequency hearing loss on speech recognition using temporal fine structure in low-frequency region
Bei Li et al.
HEARING RESEARCH (2015)
Morphological correlates of hearing loss after cochlear implantation and electro-acoustic stimulation in a hearing-impaired Guinea pig model
Lina A. J. Reiss et al.
HEARING RESEARCH (2015)
Utilizing Ethnic-Specific Differences in Minor Allele Frequency to Recategorize Reported Pathogenic Deafness Variants
A. Eliot Shearer et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
Impact of Electrode Design and Surgical Approach on Scalar Location and Cochlear Implant Outcomes
George B. Wanna et al.
LARYNGOSCOPE (2014)
Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication
Joo Hyun Park et al.
ORPHANET JOURNAL OF RARE DISEASES (2014)
Towards a consensus on a hearing preservation classification system
Henryk Skarzynski et al.
ACTA OTO-LARYNGOLOGICA (2013)
Diagnostic Application of Targeted Resequencing for Familial Nonsyndromic Hearing Loss
Byung Yoon Choi et al.
PLOS ONE (2013)
A Brief Overview of Factors Affecting Speech Intelligibility of People With Hearing Loss: Implications for Amplification
Teresa Y. C. Ching et al.
AMERICAN JOURNAL OF AUDIOLOGY (2013)
The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population
Majida Charif et al.
MOLECULAR BIOLOGY REPORTS (2012)
Long-Term Performance of Cochlear Implants in Postlingually Deafened Adults
Minoo Lenarz et al.
OTOLARYNGOLOGY-HEAD AND NECK SURGERY (2012)
A 1 bp Deletion in the Dual Reading Frame Deafness Gene LRTOMT Causes a Frameshift From the First Into the Second Reading Frame
Maarten Vanwesemael et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans
Zubair M. Ahmed et al.
NATURE GENETICS (2008)
A catechol-O-methyltransferase that is essential for auditory function in mice and humans
Xin Du et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
The importance of high-frequency audibility in the speech and language development of children with hearing loss
PG Stelmachowicz et al.
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY (2004)
Recognition of low-pass-filtered consonants in noise with normal and impaired high-frequency hearing
AR Horwitz et al.
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA (2002)