← Cor W. R. J. Cremers

Papers by Cor W. R. J. Cremers

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51. GRM7 variants confer susceptibility to age-related hearing impairmentHuman Molecular Genetics · 2008
52. Speech perception in congenitally, pre‐lingually and post‐lingually deaf children expressed in an equivalent hearing loss valueClinical Otolaryngology · 2008
53. Clinical Outcome of the Simplified Surgical Technique for BAHA ImplantationOtology & Neurotology · 2008
54. Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTAAudiology and Neurotology · 2008
55. Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like proteinHuman Molecular Genetics · 2008
56. Audiological Application Criteria for Implantable Hearing Aid Devices: A Clinical Experience at the Nijmegen ORL ClinicThe Laryngoscope · 2008
57. Predictors of future growth of sporadic vestibular schwannomas obtained by history and radiologic assessment of the tumorEuropean Archives of Oto-Rhino-Laryngology · 2008
58. Hearing Impairment in Genotyped Wolfram Syndrome PatientsAnnals of Otology Rhinology & Laryngology · 2008
59. Occupational Noise, Smoking, and a High Body Mass Index are Risk Factors for Age-related Hearing Impairment and Moderate Alcohol Consumption is Protective: A European Population-based Multicenter StudyJournal of the Association for Research in Otolaryngology · 2008
60. SIX1mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BORHuman Mutation · 2008
61. Audiometric Characteristics of a Dutch Family Linked to DFNA15 With a Novel Mutation (p.L289F) in POU4F3Archives of Otolaryngology - Head and Neck Surgery · 2008
62. Missense mutations inPOU4F3cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA bindingHuman Mutation · 2008
63. Branchio-oto-renal syndrome (BOR): novel mutations in theEYA1gene, and a review of the mutational genetics of BORHuman Mutation · 2008
64. Bone-Anchored Hearing Aid System Application for Unilateral Congenital Conductive Hearing ImpairmentOtology & Neurotology · 2008
65. The Bone-Anchored Hearing Aid for children: Recent developmentsInternational Journal of Audiology · 2008
66. The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairmentHuman Molecular Genetics · 2007
67. MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutationAmerican Journal of Medical Genetics Part A · 2007
68. SonotubometryArchives of Otolaryngology - Head and Neck Surgery · 2007
69. Phenotype description of a Dutch otosclerosis family with suggestive linkage to OTSC7American Journal of Medical Genetics Part A · 2007
70. Involvement ofDFNB59 mutations in autosomal recessive nonsyndromic hearing impairmentHuman Mutation · 2007
71. Clinical Characteristics of a Dutch DFNA9 Family with a Novel COCH Mutation, G87WAudiology and Neurotology · 2006
72. Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9)American Journal of Medical Genetics Part A · 2006
73. Rehabilitation of Patients with Conductive Hearing Loss and Moderate Mental Retardation by Means of a Bone-Anchored Hearing AidOtology & Neurotology · 2006
74. Mutations in thelipoma HMGIC fusion partner-like 5 (LHFPL5)gene cause autosomal recessive nonsyndromic hearing lossHuman Mutation · 2006
75. Audiologic Performance and Benefit of Cochlear Implantation in Usher Syndrome Type IThe Laryngoscope · 2006
76. Cochleovestibular and Ocular Features in a Dutch DFNA11 FamilyOtology & Neurotology · 2006
77. The Phenotype of the First Otosclerosis Family Linked to OTSC5Otology & Neurotology · 2006
78. Validation of sonotubometry in healthy adultsThe Journal of Laryngology & Otology · 2006
79. Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunctionHuman Molecular Genetics · 2006
80. The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1Human Molecular Genetics · 2006
81. Voice Complaints, Risk Factors for Voice Problems and History of Voice Problems in Relation to Puberty in Female Student TeachersFolia Phoniatrica et Logopaedica · 2006
82. Fitting range of the BAHA CordelleInternational Journal of Audiology · 2006
83. Prevalence of Voice Complaints, Risk Factors and Impact of Voice Problems in Female Student TeachersFolia Phoniatrica et Logopaedica · 2006
84. Utility of the Type D Scale 16 and Voice Handicap Index to Assist Voice Care in Student Teachers and TeachersFolia Phoniatrica et Logopaedica · 2006
85. Bone-Anchored Hearing Aids in Unilateral Inner Ear Deafness: An Evaluation of Audiometric and Patient Outcome MeasurementsOtology & Neurotology · 2005
86. Vestibular Deterioration Precedes Hearing Deterioration in the P51S COCH Mutation (DFNA9): An Analysis in 74 Mutation CarriersOtology & Neurotology · 2005
87. Audiometric, Vestibular, and Genetic Aspects of a DFNA9 Family with a G88E COCH MutationOtology & Neurotology · 2005
88. Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1‐22.3American Journal of Medical Genetics Part A · 2005
89. Sonotubometry: Eustachian Tube Ventilatory Function Test: A State-of-the-Art ReviewOtology & Neurotology · 2005
90. Long-term Results of Bone-Anchored Hearing Aid Recipients Who Had Previously Used Air-Conduction Hearing AidsArchives of Otolaryngology - Head and Neck Surgery · 2005
91. Does the Bone-Anchored Hearing Aid Have a Complementary Effect on Audiological and Subjective Outcomes in Patients with Unilateral Conductive Hearing Loss?Audiology and Neurotology · 2005
92. Serial Audiometry and Speech Recognition Findings in Finnish Usher Syndrome Type III PatientsAudiology and Neurotology · 2005
93. Teunissen-Cremers Syndrome: A Clinical, Surgical, and Genetic ReportOtology & Neurotology · 2005
94. Phenotype Determination Guides Swift Genotyping of a DFNA2/KCNQ4 Family With a Hot Spot Mutation (W276S)Otology & Neurotology · 2005
95. Four novelTMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing lossHuman Mutation · 2005
96. Audiological Characteristics of Some Affected Members of a Dutch DFNA13/ COL11A2 FamilyAnnals of Otology Rhinology & Laryngology · 2004
97. Variable Clinical Features in Patients with CDH23 Mutations (USH1D-DFNB12)Otology & Neurotology · 2004
98. Longitudinal Phenotypic Analysis in Patients with Connexin 26 ( GJB2 ) (DFNB1) and Connexin 30 ( GJB6 ) MutationsAnnals of Otology Rhinology & Laryngology · 2004
99. The Bone-Anchored Hearing AidArchives of Otolaryngology - Head and Neck Surgery · 2004
100. Evaluation of visual impairment in Usher syndrome 1b and Usher syndrome 2aActa Ophthalmologica Scandinavica · 2004