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Patient-preferred outcomes in patients with vestibular schwannoma: a qualitative content analysis of symptoms, side effects and their impact on health-related quality of life

Quality of life research, 2023-10, Vol.32 (10), p.2887-2897

2023

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The resilience of the inner ear—vestibular and audiometric impact of transmastoid semicircular canal plugging

Journal of neurology, 2022-10, Vol.269 (10), p.5229-5238

2022

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Skull Base Tumors: The Equilibrium between Curation and Preservation

Cancers, 2023-05, Vol.15 (10), p.2829

2023

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Gamma Knife radiosurgery for vestibular schwannomas: evaluation of tumor control and its predictors in a large patient cohort in The Netherlands

Journal of neurosurgery, 2016-06, Vol.124 (6), p.1619-1626

2016

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TcMEP threshold change is superior to A-train detection when predicting facial nerve outcome in CPA tumour surgery

Acta neurochirurgica, 2020-05, Vol.162 (5), p.1197-1203

2020

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A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis

Human genetics, 2022-04, Vol.141 (3-4), p.951-963

2022

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SDHAF2 (PGL2-SDH5) and Hereditary Head and Neck Paraganglioma

Clinical cancer research, 2011-01, Vol.17 (2), p.247-254

2011

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Skull-Base Chondrosarcoma: A Systematic Review of the Role of Postoperative Radiotherapy

Cancers, 2024-02, Vol.16 (5), p.856

2024

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Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment

American journal of human genetics, 2012-11, Vol.91 (5), p.883-889

2012

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Next-Generation Sequencing Identifies Mutations of SMPX, which Encodes the Small Muscle Protein, X-Linked, as a Cause of Progressive Hearing Impairment

American journal of human genetics, 2011-05, Vol.88 (5), p.628-634

2011

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Feasibility of a wait‐and‐scan period as initial management strategy for head and neck paraganglioma

Head & neck, 2017-10, Vol.39 (10), p.2088-2094

2017

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Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome

American journal of human genetics, 2015-04, Vol.96 (4), p.623-630

2015

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Radiomics-Based Prediction of Long-Term Treatment Response of Vestibular Schwannomas Following Stereotactic Radiosurgery

Otology & neurotology, 2020-12, Vol.41 (10), p.e1321

2020

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Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction

American journal of human genetics, 2010-04, Vol.86 (4), p.604-610

2010

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Development of a model to predict vestibular schwannoma growth: An opportunity to introduce new wait and scan strategies

Clinical otolaryngology, 2021-01, Vol.46 (1), p.273-283

2021

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Risk factors for complications in cochlear implant surgery

European archives of oto-rhino-laryngology, 2018-04, Vol.275 (4), p.895-903

2018

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Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma

Clinical cancer research, 2013-07, Vol.19 (14), p.3787-3795

2013

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Evaluation of the modified Pittsburgh classification for predicting the disease‐free survival outcome of squamous cell carcinoma of the external auditory canal

Head & neck, 2020-12, Vol.42 (12), p.3609-3622

2020

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A first exploration of the economic consequences of an autonomous surgical robot for lateral skull base surgery: an early health technology assessment

International journal of technology assessment in health care, 2023-07, Vol.39 (1), p.e46-e46, Article e46

2023

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Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment

American journal of human genetics, 2010-02, Vol.86 (2), p.138-147

2010

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Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations

Journal of the Association for Research in Otolaryngology, 2011-12, Vol.12 (6), p.753-766

2011

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Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5

European journal of human genetics : EJHG, 2015-02, Vol.23 (2), p.189-194

2015

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Disruption of Teashirt Zinc Finger Homeobox 1 Is Associated with Congenital Aural Atresia in Humans

American journal of human genetics, 2011-12, Vol.89 (6), p.813-819

2011

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Quality of life in children receiving treatment for Mycobacterium abscessus otomastoiditis

Clinical otolaryngology, 2022-07, Vol.47 (4), p.529-535

2022

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Patient-preferred outcomes in patients with vestibular schwannoma: a qualitative content analysis of symptoms, side effects and their impact on health-related quality of life

The resilience of the inner ear—vestibular and audiometric impact of transmastoid semicircular canal plugging

International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers

Skull Base Tumors: The Equilibrium between Curation and Preservation

Gamma Knife radiosurgery for vestibular schwannomas: evaluation of tumor control and its predictors in a large patient cohort in The Netherlands

TcMEP threshold change is superior to A-train detection when predicting facial nerve outcome in CPA tumour surgery

A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis

SDHAF2 (PGL2-SDH5) and Hereditary Head and Neck Paraganglioma

Skull-Base Chondrosarcoma: A Systematic Review of the Role of Postoperative Radiotherapy

Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment

Next-Generation Sequencing Identifies Mutations of SMPX, which Encodes the Small Muscle Protein, X-Linked, as a Cause of Progressive Hearing Impairment

Feasibility of a wait‐and‐scan period as initial management strategy for head and neck paraganglioma

Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome

Radiomics-Based Prediction of Long-Term Treatment Response of Vestibular Schwannomas Following Stereotactic Radiosurgery

Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction

Development of a model to predict vestibular schwannoma growth: An opportunity to introduce new wait and scan strategies

Risk factors for complications in cochlear implant surgery

Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma

Evaluation of the modified Pittsburgh classification for predicting the disease‐free survival outcome of squamous cell carcinoma of the external auditory canal

A first exploration of the economic consequences of an autonomous surgical robot for lateral skull base surgery: an early health technology assessment

Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment

Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations

Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5

Disruption of Teashirt Zinc Finger Homeobox 1 Is Associated with Congenital Aural Atresia in Humans

Quality of life in children receiving treatment for Mycobacterium abscessus otomastoiditis

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