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Cris Lanting, Ph.D.
Medical Physicist-Audiologist | Expertise in Hearing & Genes, Cochlear Implants, and Clinical Trials
Short blurb
As a Medical Physics Expert (MPE) - Audiologist, I focus on the intersection of clinical audiology, genetics, and auditory rehabilitation, emphasizing multidisciplinary collaboration to advance both patient care and scientific understanding. My work spans the discovery of genetic causes of hearing loss, e.g., the identification of a prevalent RIPOR2 mutation as a major factor in adult-onset hearing loss [(De Bruijn et al., 2021; Velde et al., 2023)], and international efforts to elucidate genotype-phenotype correlations, such as in TMPRSS3-related hearing loss [(Colbert et al., 2024)], and the evaluation of new therapies for treating sudden deafness and reducing treatment-related hearing loss in cisplatin chemoradiation [(Burger et al., 2024)].
I am committed to translating scientific insights into practical applications, exemplified by research on auditory profiling [(Lanting et al., 2022)], the development of remote cochlear implant assessments [(Wasmann et al., 2024)], and the evaluation of sound-level reduction interventions in critical care settings [(Vreman et al., 2024)]. Through collaborations with national and European networks and active participation in clinical trials, I aim to improve diagnostics, therapeutic options, and patient outcomes in audiology.
In addition to research, I contribute to academic and clinical audiology through teaching, supervision of Ph.D. students, and involvement in committees that promote team science and advance evidence-based care.
Clinical expertise:
In my clinical practice, I focus on providing comprehensive care for patients with complex auditory needs:
- Expertise Center Hearing & Implants As part of the largest implant center in the Netherlands, I contribute to a multidisciplinary “one-stop shop” for hearing rehabilitation, including cochlear implants and middle ear implants.
- Expertise Center Hearing & Genes I work within a multidisciplinary team addressing hereditary hearing loss, as part of the European Reference Network ERN-CRANIO.
- DOOFNL Diagnostiek & Onderzoek Oto-genotype Fenotype NederLand: I am involved in this unique collaboration of academic centers (ENT specialists, clinical geneticists, and audiologists) to advance the diagnosis and understanding of rare hearing disorders.
- Clinical Audiology: I specialize in diagnostics for pediatric hearing loss, including complex cases, and cochlear implants for children.
- Tinnitus and Hyperacusis: I provide diagnostics and management for these conditions.
- Accessibility of Care: I am engaged in developing regional care networks involving GPs, ENTs, and audiologists to improve access and streamline care pathways.
Academic focus:
My academic focus complements this clinical expertise and drives innovation in the field:
- Hearing and Genes: I investigate the perceptual consequences of genetic mutations, underlying mechanisms, and site-of-lesion testing, as demonstrated in several key publications (see e.g. research output).
- Auditory Profiling: I develop tools and methodologies to characterize auditory performance and measure outcomes.
- Inner Ear Therapy and Clinical Trials: I participate in Phase 1/2 trials, including therapies targeting gene defects and sudden deafness, with translational impact on patient care.
- Evaluation of Auditory Implants: My work includes sponsor-driven investigations of new implants and long-term evaluations of cochlear and middle ear implants, refining indication criteria and obtaining functional outcome measures.
This integration of clinical expertise and academic focus reflects my commitment to advancing audiological care through evidence-based practices, collaborative networks, and patient-centered innovation.
Experience
Radboud University Medical Center
2018 – Present | Medical Physics Expert (MPE) - Audiologist
- Expertise in hereditary hearing loss, cochlear implants, tinnitus, hyperacusis, and pediatric diagnostics.
- Phase 1 & 2 clinical trials for inner ear therapies (press release).
- Academic focus on genetic hearing loss, site-of-lesion testing, and auditory performance metrics.
University Medical Center Groningen
2013 – 2017 | Medical Physics Expert (MPE) - Audiologist in training
- Focus on tinnitus neuroimaging standards within TINNET.
- Contributed to national audiology training networks via KKAu.
- Board member of KLIFOP representing medical physicists in training.
Medical Research Councel (MRC) Institute of Hearing Research, Nottingham
2009 – 2012 | Career Development Fellow
- Research on ultrahigh-resolution fMRI of the auditory cortex at the MRC IHR.
- Investigated cortical frequency selectivity using EEG methods in collaboration with the SPMMRC.
University of Groningen
2005 – 2009 | Ph.D. in Biomedical Sciences
- Thesis: Functional Magnetic Resonance Imaging of Tinnitus.
- Focus on auditory neuroscience of tinnitus and imaging of brain activity.
- Defense date: March 31, 2010 (PDF).
Education
University of Groningen
1999 – 2005 | M.Sc. Applied Physics
- Specialized in Biomedical Engineering — Medical Imaging.
- Thesis: Perfusion Imaging using Arterial Spin Labeling.
Wessel Gansfort College
1993 – 1999 | Pre-University Education (VWO)
Certification and course
- 2024 Leergang Begeleiden van Promovendi / Supervising PhDs at Radboudumc.
- 2023 ISO 14155: 2020 Good Clinical Practice (GCP) for Site Staff}. Cochlear Academy
- 2022 ICH GOOD CLINICAL PRACTICE (GCP) E6 (R2)}. Globalhealthtrainingcentre.org/elearning
- 2019 Teach the teacher/Opleiden van aios in de klinische praktijk (OKP)
- **2017 NFU Basic Course Regulations and Organization for Clinical Investigators (BROK)} currently undergoing re-certification
Grants and Awards
- 2024: Donders Research Stimulation Fund 2024; “Ear and Hearing Focus group”
- 2024: Donders Research Stimulation Fund 2024; Collaboration fund with Marc van Wanrooij “Enhancing Auditory Profiles: A Cross-Center Approach to Understanding and Addressing Hearing Loss”
- 2022: Investigator Initiated Research (IIR) Grant with Cochlear Ltd on Genetic hearing loss influences outcomes of cochlear implantation, a PhD project 2020-2023
- 2011: Nomination for Best Ph.D. Thesis, BCN
- 2010: Thesis Grants
Committees and Activities
- Editor at Audiologieboek.nl, a National audiology syllabus
- Member of the Nederlandse Vereniging voor Klinisch Fysica (NKKF Wetenschap en Innovatie); developed a Kennisagenda 2020-2025
- User Committee, NWO TTW Project: OtoControl-2.0 (2024–2029)
- Member of the Kerngroep Klinische Audiologen (KKAu)
- Scientific Audiology advisor at ENT Clinical
- Member of the Workgroup Kennisagenda in de Kwaliteitscyclus of the NVKNO (development of a 3rd version of a Kennisagenda)
- Chair of the Workgroup Kennisagenda 2.0 of the NVKF (development of a 2nd version of a Kennisagenda 2025-2029)
- Member of the National Scientific Committee ESPCI 2023 Rotterdam
- Member of the Workgroup Neuroimaging COST action TINNET (Cost action BM1306)
Teaching and Supervision
Teaching
- 2023 - Now: Guest lecture Donderd Neurophysics course Physics of the The Auditory System: Hearing Impairment
- 2018 – Now: Lecturer, Minor Clinical Genomics, Radboudumc
- 2018 - 2022: Organised monthly Hearing & Implants meeting at Radboudumc and Donders Centre for Neuroscience, Department of Biophysics
- 2015 – 2017: Lecturer Capita Selecta, “From Sound to Hearing,” University of Groningen
- 2013 – 2017: Lecturer, Lecturer Vector Calculus and Mathematics for Neuroscientists, University of Groningen, Graduate school Behavioral and Cognitive Neurosciences
- 2005 – 2009: Lecturer fMRI Course Research Master, University of Groningen, Graduate school Behavioral and Cognitive Neurosciences
Supervision
- Ph.D. Students: Supervision as copromotor for ENT residents within the theme of Hearing & Genes, Hearing & Implants and Audiology (7 ongoing, 2 finished)
- Medical Physicists in Training: supervised two trainees for their scientific project
Research Output
Selected publications
- (De Bruijn et al., 2021)
- (Velde et al., 2023)
- (Colbert et al., 2024)
- (Lanting et al., 2022)
- (Wasmann et al., 2024)
- (Lanting et al., 2025)
Complete list
Journal Articles
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Vreman, J., Lanting, C., Frenzel, T., van der Hoeven, J. G., Lemson, J., & van den Boogaard, M. (2026). The Impact of a Noise Reduction Bundle on ICU Staff: A Stepped-Wedge Cluster Randomized Clinical Trial. Intensive and Critical Care Nursing, 93, 104306. https://doi.org/10.1016/j.iccn.2025.104306
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Fehrmann, M., Beynon, A., Huinck, W., Pennings, R., Mylanus, E., & Lanting, C. (2025). The Potential of Electrocochleography in Explaining the Variability in Cochlear Implant Outcomes: A Scoping Review. International Journal of Audiology, 1–15. https://doi.org/10.1080/14992027.2025.2459223
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Fehrmann, M. L. A., Haer-Wigman, L., Kremer, H., Yntema, H. G., Thijssen, M. E. G., Mylanus, E. A. M., Huinck, W. J., Lanting, C. P., & Pennings, R. J. E. (2025). Cochlear Implantation Outcomes in Genotyped Subjects with Sensorineural Hearing Loss. Journal of the Association for Research in Otolaryngology. https://doi.org/10.1007/s10162-025-00987-0
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Wijn, D. H., Fehrmann, M. L. A., Robijn, S. M. M., Velde, H. M., Smits, J. J., van Wijk, E., Beynon, A. J., Cals, F. L. J., Hoyng, C. B., Yzer, S., Lanting, C. P., & Pennings, R. J. E. (2025). From Sound to Stability: Lessons Learned From the CRUSH Study on Hearing Loss Progression and Vestibular Phenotype in Usher Syndrome Type 2A. Otology & Neurotology, 10.1097/MAO.0000000000004851. https://doi.org/10.1097/MAO.0000000000004851
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Lanting, C., Robijn, S., Nieratschker, M., Galetzka, C., Meis, A., Rommelspacher, H., Ahoud-Schoenmakers, S., Lackner, E., Zeitlinger, M., Bauer, M., Arnoldner, C., Pennings, R., & Schlingensiepen, R. (2025). Assessment of Safety, Tolerability, Pharmacokinetics, and Volume-Dependent Conductive Hearing Loss in Healthy Volunteers: First-in-Human, Open-Label, Placebo-Controlled Study of a Single Intratympanic Injection of AC102. Otology & Neurotology, 46(8), 884–894. https://doi.org/10.1097/MAO.0000000000004568
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Lanting, C. P. (2025). Geluid op de OK en daarbuiten. Operationeel, 2025(5), 84–87.
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Wasmann, J.-W. A., Huinck, W. J., & Lanting, C. P. (2024). Remote Cochlear Implant Assessments: Validity and Stability in Self-Administered Smartphone-Based Testing. Ear and Hearing, 45(1), 239–249. https://doi.org/10.1097/AUD.0000000000001422
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Kemps, G., Geven, L., Kunst, H., Mylanus, E., Mulder, J., Lanting, C., & Pennings, R. (2024). Surgical Treatment for Troublesome Mastoid Cavities: Canal Wall Reconstruction With Bony Obliteration Versus Subtotal Petrosectomy. Otology & Neurotology: Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 45(3), 273–280. https://doi.org/10.1097/MAO.0000000000004109
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Colbert, B. M., Lanting, C., Smeal, M., Blanton, S., Dykxhoorn, D. M., Tang, P.-C., Getchell, R. L., Velde, H., Fehrmann, M., Thorpe, R., Chapagain, P., Elkhaligy, H., Kremer, H., Yntema, H., Haer-Wigman, L., Redfield, S., Sun, T., Bruijn, S., Plomp, A., … Liu, X. Z. (2024). The Natural History and Genotype–Phenotype Correlations of TMPRSS3 Hearing Loss: An International, Multi-Center, Cohort Analysis. Human Genetics, 143(5), 721–734. https://doi.org/10.1007/s00439-024-02648-3
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Fehrmann, M. L. A., Meijer, F. J. A., Mylanus, E. A. M., Pennings, R. J. E., Lanting, C. P., & Huinck, W. J. (2024). Evaluating Cochlear Implant Outcomes in DFNA9 Subjects: A Comprehensive Study on Cerebral White Matter Lesions and Vestibular Abnormalities. European Archives of Oto-Rhino-Laryngology. https://doi.org/10.1007/s00405-024-08933-1
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Fehrmann, M. L. A., Lanting, C. P., Haer-Wigman, L., Mylanus, E. A. M., Huinck, W. J., & Pennings, R. J. E. (2024). Good Cochlear Implantation Outcomes in Subjects with Mono-Allelic WFS1- Associated Sensorineural Hearing Loss – a Case Series. International Journal of Audiology, 1–9. https://doi.org/10.1080/14992027.2024.2411579
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Velde, H. M., Vaseghi-Shanjani, M., Smits, J. J., Ramakrishnan, G., Oostrik, J., Wesdorp, M., Astuti, G., Yntema, H. G., Hoefsloot, L., Lanting, C. P., Huynen, M. A., Lehman, A., Turvey, S. E., DOOFNL Consortium, Aten, E., Van Den Boogaard, M. J., Cals, F. L. J., Van Dooren, M. F., Ebbens, F. A., … Kremer, H. (2024). Exome Variant Prioritization in a Large Cohort of Hearing-Impaired Individuals Indicates IKZF2 to Be Associated with Non-Syndromic Hearing Loss and Guides Future Research of Unsolved Cases. Human Genetics, 143(11), 1379–1399. https://doi.org/10.1007/s00439-024-02706-w
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Fehrmann, M. L. A., Lanting, C. P., Haer-Wigman, L., Yntema, H. G., Mylanus, E. A. M., Huinck, W. J., & Pennings, R. J. E. (2024). Long-Term Outcomes of Cochlear Implantation in Usher Syndrome. Ear and Hearing, 10.1097/AUD.0000000000001544. https://doi.org/10.1097/AUD.0000000000001544
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Vreman, J., Cris, L., Frenzel, T., van der Hoeven, J., Lemson, J., & van den Boogaard, M. (2024). Reduction of Sound Levels in the Intermediate Care Unit; a Quasi-Experimental Time-Series Design Study. Intensive and Critical Care Nursing, 85, 103810. https://doi.org/10.1016/j.iccn.2024.103810
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Velde, H. M., Huizenga, X. J. J., Yntema, H. G., Haer-Wigman, L., Beynon, A. J., Oostrik, J., Pegge, S. A. H., Kremer, H., Lanting, C. P., & Pennings, R. J. E. (2023). Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38. Genes, 14(2), 457. https://doi.org/10.3390/genes14020457
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Vreman, J., Lemson, J., Lanting, C., van der Hoeven, J., & van den Boogaard, M. (2023). The Effectiveness of the Interventions to Reduce Sound Levels in the ICU: A Systematic Review. Critical Care Explorations, 5(4), e0885. https://doi.org/10.1097/CCE.0000000000000885
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Velde, H. M., Homans, N. C., Goedegebure, A., Lanting, C. P., Pennings, R. J. E., & Kremer, H. (2023). Analysis of Rotterdam Study Cohorts Confirms a Previously Identified RIPOR2 In-Frame Deletion as a Prevalent Genetic Factor in Phenotypically Variable Adult-Onset Hearing Loss (DFNA21) in the Netherlands. Journal of Medical Genetics, 60(11), 1061–1066. https://doi.org/10.1136/jmg-2023-109146
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Fehrmann, M. L. A., Huinck, W. J., Thijssen, M. E. G., Haer-Wigman, L., Yntema, H. G., Rotteveel, L. J. C., Widdershoven, J. C. C., Goderie, T., Van Dooren, M. F., Hoefsloot, E. H., Van Der Schroeff, M. P., Mylanus, E. A. M., DOOFNL consortium, Van Dooren, M. F., Kant, S. G., De Gier, H. H. W., Hoefsloot, E. H., Van Der Schroeff, M. P., Rotteveel, L. J. C., … Pennings, R. J. E. (2023). Stable Long-Term Outcomes after Cochlear Implantation in Subjects with TMPRSS3 Associated Hearing Loss: A Retrospective Multicentre Study. Journal of Otolaryngology - Head & Neck Surgery, 52(1), 82. https://doi.org/10.1186/s40463-023-00680-3
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Robijn, S. M. M., Smits, J. J., Sezer, K., Huygen, P. L. M., Beynon, A. J., Van Wijk, E., Kremer, H., De Vrieze, E., Lanting, C. P., & Pennings, R. J. E. (2022). Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis. Biomolecules, 12(2), 220. https://doi.org/10.3390/biom12020220
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Smits, J. J., de Bruijn, S. E., Lanting, C. P., Oostrik, J., O’Gorman, L., Mantere, T., DOOFNL Consortium, Cremers, F. P. M., Roosing, S., Yntema, H. G., de Vrieze, E., Derks, R., Hoischen, A., Pegge, S. A. H., Neveling, K., Pennings, R. J. E., & Kremer, H. (2022). Exploring the Missing Heritability in Subjects with Hearing Loss, Enlarged Vestibular Aqueducts, and a Single or No Pathogenic SLC26A4 Variant. Human Genetics, 141(3-4), 465–484. https://doi.org/10.1007/s00439-021-02336-6
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Smits, J. J., De Bruijn, S. E., Lanting, C. P., Oostrik, J., O’Gorman, L., Mantere, T., DOOFNL Consortium, Van Dooren, M. F., Kant, S. G., De Gier, H. H. W., Hoefsloot, E. H., Van Der Schroeff, M. P., Rotteveel, L. J. C., Ropers, F. G., Widdershoven, J. C. C., Hof, J. R., Vanhoutte, E. K., Feenstra, I., Kremer, H., … Kremer, H. (2022). Correction to: Exploring the Missing Heritability in Subjects with Hearing Loss, Enlarged Vestibular Aqueducts, and a Single or No Pathogenic SLC26A4 Variant. Human Genetics, 141(3-4), 991–991. https://doi.org/10.1007/s00439-021-02377-x
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Consensus Statement on Bone Conduction Devices and Active Middle Ear Implants in Conductive and Mixed Hearing Loss. (2022). Otology & Neurotology, 43(5), 513–529. https://doi.org/10.1097/MAO.0000000000003491
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Lanting, C., Snik, A., Leijendeckers, J., Bosman, A., & Pennings, R. (2022). Genetic Hearing Loss Affects Cochlear Processing. Genes, 13(11), 1923. https://doi.org/10.3390/genes13111923
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Velde, H. M., Reurink, J., Held, S., Li, C. H. Z., Yzer, S., Oostrik, J., Weeda, J., Haer-Wigman, L., Yntema, H. G., Roosing, S., Pauleikhoff, L., Lange, C., Whelan, L., Dockery, A., Zhu, J., Keegan, D. J., Farrar, G. J., Kremer, H., Lanting, C. P., … Pennings, R. J. E. (2022). Usher Syndrome Type IV: Clinically and Molecularly Confirmed by Novel ARSG Variants. Human Genetics, 141(11), 1723–1738. https://doi.org/10.1007/s00439-022-02441-0
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Wasmann, J.-W. A., Lanting, C. P., Cris P. Lanting, Huinck, W. J., Mylanus, E. A. M., van der Laak, J. W. M., Govaerts, P., De Wet Swanepoel, Moore, D. R., & Barbour, D. L. (2021). Computational Audiology: New Approaches to Advance Hearing Health Care in the Digital Age. Ear and Hearing. https://doi.org/10.1097/aud.0000000000001041
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De Bruijn, S. E., Smits, J. J., Liu, C., Lanting, C. P., Beynon, A. J., Blankevoort, J., Oostrik, J., Koole, W., De Vrieze, E., Cremers, C. W. R. J., Cremers, F. P. M., Roosing, S., Yntema, H. G., Kunst, H. P. M., Zhao, B., Pennings, R. J. E., & Kremer, H. (2021). A RIPOR2 In-Frame Deletion Is a Frequent and Highly Penetrant Cause of Adult-Onset Hearing Loss. Journal of Medical Genetics, 58(2), 96–104. https://doi.org/10.1136/jmedgenet-2020-106863
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Smits, J. J., Van Beelen, E., Weegerink, N. J. D., Oostrik, J., Huygen, P. L. M., Beynon, A. J., Lanting, C. P., Kunst, H. P. M., Schraders, M., Kremer, H., De Vrieze, E., & Pennings, R. J. E. (2021). A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 Phenotype. Otology & Neurotology, 42(4), e399–e407. https://doi.org/10.1097/MAO.0000000000003004
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Chen, T., Rohacek, A. M., Caporizzo, M., Nankali, A., Smits, J. J., Oostrik, J., Lanting, C. P., Kücük, E., Gilissen, C., van de Kamp, J. M., Pennings, R. J. E., Rakowiecki, S. M., Kaestner, K. H., Ohlemiller, K. K., Oghalai, J. S., Kremer, H., Prosser, B. L., & Epstein, D. J. (2021). Cochlear Supporting Cells Require GAS2 for Cytoskeletal Architecture and Hearing. Developmental Cell, 56(10), 1526–1540.e7. https://doi.org/10.1016/j.devcel.2021.04.017
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Koops, E. A., Renken, R. J., Lanting, C. P., & Van Dijk, P. (2020). Cortical Tonotopic Map Changes in Humans Are Larger in Hearing Loss Than in Additional Tinnitus. The Journal of Neuroscience, 40(16), 3178–3185. https://doi.org/10.1523/JNEUROSCI.2083-19.2020
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Besle, J., Mougin, O., Sánchez-Panchuelo, R.-M., Lanting, C., Gowland, P., Bowtell, R., Francis, S., & Krumbholz, K. (2019). Is Human Auditory Cortex Organization Compatible With the Monkey Model? Contrary Evidence From Ultra-High-Field Functional and Structural MRI. Cerebral Cortex, 29(1), 410–428. https://doi.org/10.1093/cercor/bhy267
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DOOFNL Consortium, Smits, J. J., Oostrik, J., Beynon, A. J., Kant, S. G., De Koning Gans, P. A. M., Rotteveel, L. J. C., Klein Wassink-Ruiter, J. S., Free, R. H., Maas, S. M., Van De Kamp, J., Merkus, P., Koole, W., Feenstra, I., Admiraal, R. J. C., Lanting, C. P., Schraders, M., Yntema, H. G., Pennings, R. J. E., & Kremer, H. (2019). De Novo and Inherited Loss-of-Function Variants of ATP2B2 Are Associated with Rapidly Progressive Hearing Impairment. Human Genetics, 138(1), 61–72. https://doi.org/10.1007/s00439-018-1965-1
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Lanting, C. P., De Kleine, E., Langers, D. R. M., & Van Dijk, P. (2014). Unilateral Tinnitus: Changes in Connectivity and Response Lateralization Measured with fMRI. PLoS ONE, 9(10), e110704. https://doi.org/10.1371/journal.pone.0110704
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Lanting, C. P., Briley, P. M., Sumner, C. J., & Krumbholz, K. (2013). Mechanisms of Adaptation in Human Auditory Cortex. Journal of Neurophysiology, 110(4), 973–983. https://doi.org/10.1152/jn.00547.2012
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Crippa, A., Lanting, C. P., van Dijk, P., & Roerdink, J. B. T. M. (2010). A Diffusion Tensor Imaging Study on the Auditory System and Tinnitus. The Open Neuroimaging Journal, 4(1). https://doi.org/10.2174/1874440001004010016
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Lanting, C. P., De Kleine, E., Eppinga, R. N., & Van Dijk, P. (2010). Neural Correlates of Human Somatosensory Integration in Tinnitus. Hearing Research, 267(1-2), 78–88. https://doi.org/10.1016/j.heares.2010.04.006
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Lanting, C. P., De Kleine, E., & Van Dijk, P. (2009). Neural Activity Underlying Tinnitus Generation: Results from PET and fMRI. Hearing Research, 255(1-2), 1–13. https://doi.org/10.1016/j.heares.2009.06.009
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Lanting, C. P., De Kleine, E., Bartels, H., & Van Dijk, P. (2008). Functional Imaging of Unilateral Tinnitus Using fMRI. Acta Oto-Laryngologica, 128(4), 415–421. https://doi.org/10.1080/00016480701793743
Conference Articles
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Lanting, C., Schlingensiepen, R., Rommelspacher, H., Galetzka, C., Meis, A., & Nieratschker, M. (2024). Clinical Development of AC102 for the Treatment of Sudden Sensorineural Hearing Loss. DGHNO-KHC Annual Meeting 2024, 103(S 02), S283–S284. https://doi.org/10.1055/s-0044-1784948
Books
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Van Dijk, P., Başkent, D., Gaudrain, E., De Kleine, E., Wagner, A., & Lanting, C. (Eds.). (2016). Physiology, Psychoacoustics and Cognition in Normal and Impaired Hearing (Vol. 894). Springer International Publishing. https://doi.org/10.1007/978-3-319-25474-6
Book Chapters
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Lanting, C., WoźAniak, A., Van Dijk, P., & Langers, D. R. M. (2016). Tinnitus- and Task-Related Differences in Resting-State Networks. In P. Van Dijk, D. Başkent, E. Gaudrain, E. De Kleine, A. Wagner, & C. Lanting (Eds.), Physiology, Psychoacoustics and Cognition in Normal and Impaired Hearing (Vol. 894, pp. 175–187). Springer International Publishing. https://doi.org/10.1007/978-3-319-25474-6_19
Digital Presence
Last updated: November 2025