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

od Hendriks, Tom, Kunst, Henricus P. M., Huppelschoten, Maarten, Doorduin, Jonne, Ter Laan, Mark
izdano v Acta Neurochir (Wien) (2020)

Pulsatile Tinnitus: Differential Diagnosis and Radiological Work-Up

od Pegge, Sjoert A. H., Steens, Stefan C. A., Kunst, Henricus P. M., Meijer, Frederick J. A.
izdano v Curr Radiol Rep (2017)

Quality of life, social function, emotion, and facial paresis in Dutch vestibular schwannoma patients

od Blom, Stephanie S. A. H., Aarts, Henk, Wever, Capi C., Kunst, Henricus P. M., Semin, Gün R.
izdano v Laryngoscope Investig Otolaryngol (2020)

Lateralization of facial emotion processing and facial paresis in Vestibular Schwannoma patients

od Blom, Stephanie S. A. H., Aarts, Henk, Kunst, Henricus P. M., Wever, Capi C., Semin, Gün R.
izdano v Brain Behav (2020)

What determines quality of life in patients with vestibular schwannoma?

od Pruijn, Ineke M. J., Kievit, Wietske, Hentschel, Mayke A., Mulder, Jef J. S., Kunst, Henricus P. M.
izdano v Clin Otolaryngol (2020)

Audiological Evaluation of Affected Members from a Dutch DFNA8/12 (TECTA) Family

od Plantinga, Rutger F., Cremers, Cor W.R.J., Huygen, Patrick L.M., Kunst, Henricus P.M., Bosman, Arjan J.
Izdano 2006

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

od Hentschel, Mayke A., Hannink, Gerjon, Steens, Stefan C. A., Mulder, Jef J. S., Rovers, Maroeska M., Kunst, Henricus P. M.
izdano v Clin Otolaryngol (2020)

Auricular prostheses attached to osseointegrated implants: multidisciplinary work-up and clinical evaluation

od Vijverberg, Maarten A., Verhamme, Luc, van de Pol, Pascal, Kunst, Henricus P. M., Mylanus, Emmanuel A. M., Hol, Myrthe K. S.
izdano v Eur Arch Otorhinolaryngol (2019)

Clinical relevance of occipital condyle fractures

od van der Burg, Stijn J, Pouw, Martin H, Brink, Monique, Dekker, Helena, Kunst, Henricus P M, Hosman, Allard J F
izdano v J Craniovertebr Junction Spine (2020)

In search of the most cost‐effective monitoring strategy for vestibular schwannoma: A decision analytical modelling study

od Scholte, Mirre, Hentschel, Mayke A., Hannink, Gerjon, Kunst, Henricus P. M., Steens, Stefan C., Rovers, Maroeska M., Grutters, Janneke P. C.
izdano v Clin Otolaryngol (2019)

A Novel TECTA Mutation in a Dutch DFNA8/12 Family Confirms Genotype–Phenotype Correlation

od Plantinga, Rutger F., de Brouwer, Arjan P.M., Huygen, Patrick L.M., Kunst, Henricus P.M., Kremer, Hannie, Cremers, Cor W.R.J.
Izdano 2006

Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1

od Hogewind, Barend F.T., Pennings, Ronald J.E., Hol, Frans A., Kunst, Henricus P.M., Hoefsloot, Elisabeth H., Cruysberg, Johannes R.M., Cremers, Cor W.R.J.
Izdano 2010

Paediatric Cochlear Implantation in Patients with Waardenburg Syndrome

od van Nierop, Josephine W.I., Snabel, Rebecca R., Langereis, Margreet, Pennings, Ronald J.E., Admiraal, Ronald J.C., Mylanus, Emmanuel A.M., Kunst, Henricus P.M.
izdano v Audiol Neurootol (2016)

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

od Schraders, Margit, Oostrik, Jaap, Huygen, Patrick L.M., Strom, Tim M., van Wijk, Erwin, Kunst, Henricus P.M., Hoefsloot, Lies H., Cremers, Cor W.R.J., Admiraal, Ronald J.C., Kremer, Hannie
Izdano 2010

Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome

od Bunn, Kieran J., Daniel, Phil, Rösken, Heleen S., O’Neill, Adam C., Cameron-Christie, Sophia R., Morgan, Tim, Brunner, Han G., Lai, Angeline, Kunst, Henricus P.M., Markie, David M., Robertson, Stephen P.
izdano v Am J Hum Genet (2015)

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

od Schraders, Margit, Haas, Stefan A., Weegerink, Nicole J.D., Oostrik, Jaap, Hu, Hao, Hoefsloot, Lies H., Kannan, Sriram, Huygen, Patrick L.M., Pennings, Ronald J.E., Admiraal, Ronald J.C., Kalscheuer, Vera M., Kunst, Henricus P.M., Kremer, Hannie
Izdano 2011

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

od Weegerink, Nicole J. D., Schraders, Margit, Oostrik, Jaap, Huygen, Patrick L. M., Strom, Tim M., Granneman, Susanne, Pennings, Ronald J. E., Venselaar, Hanka, Hoefsloot, Lies H., Elting, Mariet, Cremers, Cor W. R. J., Admiraal, Ronald J. C., Kremer, Hannie, Kunst, Henricus P. M.
Izdano 2011

Similar phenotypes caused by mutations in OTOG and OTOGL

od Oonk, Anne M.M., Leijendeckers, Joop M., Huygen, Patrick L.M., Schraders, Margit, del Campo, Miguel, del Castillo, Ignacio, Tekin, Mustafa, Feenstra, Ilse, Beynon, Andy J., Kunst, Henricus P.M., Snik, Ad F.M., Kremer, Hannie, Admiraal, Ronald J.C., Pennings, Ronald J.E.
Izdano 2014

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

od Bespalova, Irina N., Van Camp, Guy, Bom, Steven J.H., Brown, David J., Cryns, Kim, DeWan, Andrew T., Erson, Ayse E., Flothmann, Kris, Kunst, Henricus P.M., Kurnool, Purnima, Sivakumaran, Theru A., Cremers, Cor W.R.J., Leal, Suzanne M., Burmeister, Margit, Lesperance, Marci M.
izdano v Hum Mol Genet (2001)

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

od Schraders, Margit, Lee, Kwanghyuk, Oostrik, Jaap, Huygen, Patrick L.M., Ali, Ghazanfar, Hoefsloot, Lies H., Veltman, Joris A., Cremers, Frans P.M., Basit, Sulman, Ansar, Muhammad, Cremers, Cor W.R.J., Kunst, Henricus P.M., Ahmad, Wasim, Admiraal, Ronald J.C., Leal, Suzanne M., Kremer, Hannie
Izdano 2010