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← Cor W. R. J. Cremers

Papers by Cor W. R. J. Cremers

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  1. Bone-Anchored Hearing Aid in Unilateral Inner Ear Deafness: A Study of 20 PatientsAudiology and Neurotology · 2004
  2. Candidacy for the Bone-Anchored Hearing AidAudiology and Neurotology · 2004
  3. Evidence of progression and fluctuation of hearing impairment in branchio-oto-renal syndromeInternational Journal of Audiology · 2004
  4. A Novel Mutation Identified in the DFNA5 Gene in a Dutch Family: A Clinical and Genetic EvaluationAudiology and Neurotology · 2003
  5. Sex-Related Hearing Impairment in Wolfram Syndrome Patients Identified by Inactivating WFS1 MutationsAudiology and Neurotology · 2003
  6. Congenital Aural Atresia in 18q Deletion or de Grouchy SyndromeOtology & Neurotology · 2003
  7. Stapes Surgery in Osteogenesis Imperfecta: Results of a New SeriesOtology & Neurotology · 2003
  8. Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric diseaseHuman Mutation · 2003
  9. Progression of Low-Frequency Sensorineural Hearing Loss (DFNA6/14-WFS1)Archives of Otolaryngology - Head and Neck Surgery · 2003
  10. Cross-Sectional Analysis of Hearing Threshold in Relation to Age in a Large Family with Cochleovestibular Impairment Thoroughly Genotyped for DFNA9/ COCHAnnals of Otology Rhinology & Laryngology · 2003
  11. Bone-anchored Hearing Aids in Unilateral Inner Ear DeafnessActa Oto-Laryngologica · 2003
  12. Congenital Conductive Hearing Loss in DyschondrosteosisAnnals of Otology Rhinology & Laryngology · 2003
  13. Effect of Exogenous Surfactant on Ventilatory and Clearance Function of the Rat's Eustachian TubeOtology & Neurotology · 2003
  14. Characterizing and Distinguishing Progressive Phenotypes in Nonsyndromic Autosomal Dominant Hearing ImpairmentHearing Balance and Communication · 2003
  15. Pure Tone Hearing Thresholds and Speech Recognition Scores in Dutch Patients Carrying Mutations in the USH2A GeneOtology & Neurotology · 2003
  16. A Review of Progressive Phenotypes in Nonsyndromic Autosomal Dominant Hearing ImpairmentHearing Balance and Communication · 2003
  17. Craniofacial Titanium Implants and Chronic Pain: Histologic FindingsOtology & Neurotology · 2002
  18. Autosomal Dominant Low-Frequency Hearing Impairment (DFNA6/14)Otology & Neurotology · 2002
  19. Inner Ear Anomalies Are Frequent but Nonobligatory Features of the Branchio-oto-renal SyndromeArchives of Otolaryngology - Head and Neck Surgery · 2002
  20. A mutational hot spot in theKCNQ4 gene responsible for autosomal dominant hearing impairmentHuman Mutation · 2002
  21. Longitudinal and Cross-Sectional Phenotype Analysis in a New, Large Dutch DFNA2/ KCNQ4 FamilyAnnals of Otology Rhinology & Laryngology · 2002
  22. Temporal Bone Anomalies in the Branchio-Oto-Renal Syndrome: Detailed Computed Tomographic and Magnetic Resonance Imaging FindingsOtology & Neurotology · 2002
  23. Differences in Endolymphatic Sac Mitochondria‐Rich Cells Indicate Specific FunctionsThe Laryngoscope · 2002
  24. The Bone-Anchored Hearing Aid in Patients with a Unilateral Air-Bone GapOtology & Neurotology · 2002
  25. Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a familyClinical Otolaryngology · 2001
  26. Speech Recognition Scores Related to Age and Degree of Hearing Impairment in DFNA2/KCNQ4 and DFNA9/COCHArchives of Otolaryngology - Head and Neck Surgery · 2001
  27. A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutationJournal of Medical Genetics · 2001
  28. Histopathologic Features of the Temporal Bone in Usher Syndrome Type IArchives of Otolaryngology - Head and Neck Surgery · 2000
  29. Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21)Clinical Otolaryngology · 2000
  30. Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore regionAmerican Journal of Medical Genetics · 2000
  31. Progressive Cochleovestibular Impairment Caused by a Point Mutation in the COCH Gene at DFNA9The Laryngoscope · 1999
  32. A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusJournal of Medical Genetics · 1999
  33. The BAHA HC200/300 in comparison with conventional bone conduction hearing aidsClinical Otolaryngology · 1999
  34. Hearing Impairment Related to Age in Usher Syndrome Types 1B and 2AArchives of Otolaryngology - Head and Neck Surgery · 1999
  35. Genetic heterogeneity associated with branchio-oto-renal syndromeAmerican Journal of Medical Genetics · 1999
  36. Semen Analysis in the Usher Syndrome Type 2AORL · 1999
  37. Autosomal Dominant Non-syndromal Low-frequency Sensorineural Hearing Impairment Linked to Chromosome 4p16 (DFNA14): Statistical Analysis of Hearing Threshold in Relation to Age and Evaluation of Vestibulo-ocular FunctionsInternational Journal of Audiology · 1999
  38. Diagnosis and Management Strategies in Congenital Atresia of the External Auditory CanalBritish Journal of Audiology · 1999
  39. Non-Syndromal Autosomal Dominant Hearing Impairment: Ongoing Phenotypical Characterization of GenotypesBritish Journal of Audiology · 1999
  40. Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIaScience · 1998
  41. Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) Gene at 8q13American Journal of Medical Genetics · 1998
  42. Audiometric Results of Bilateral Bone‐Anchored Hearing Aid Application in Patients With Bilateral Congenital Aural AtresiaThe Laryngoscope · 1998
  43. Short- and Long-term Results With Implantable Transcutaneous and Percutaneous Bone-Conduction DevicesArchives of Otolaryngology - Head and Neck Surgery · 1998
  44. Binaural Application of the Bone-Anchored Hearing AidAnnals of Otology Rhinology & Laryngology · 1998
  45. A New More Powerful Bone-Anchored Hearing Aid: First ResultsScandinavian Audiology · 1998
  46. Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndromeHuman Mutation · 1998
  47. Nonsyndromic Autosomal Dominant Progressive Sensorineural Hearing Loss: Audiologic Analysis of a Pedigree Linked to DFNA2The Laryngoscope · 1998
  48. Inherited Nonsyndromic Hearing Loss: An Audiovestibular Study in a Large Family With Autosomal Dominant Progressive Hearing Loss Related to DFNA2Archives of Otolaryngology - Head and Neck Surgery · 1997
  49. The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: Identification of a somatic mosaicism for aPOU3F4 missense mutationHuman Mutation · 1997
  50. Branchio-Oto-Renal Syndrome: Identification of Novel Mutations, Molecular Characterization, Mutation Distribution, and Prospects for Genetic TestingGenetic Testing · 1997