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

Por Hendriks, Tom, Kunst, Henricus P. M., Huppelschoten, Maarten, Doorduin, Jonne, Ter Laan, Mark
Publicado no Acta Neurochir (Wien) (2020)

Pulsatile Tinnitus: Differential Diagnosis and Radiological Work-Up

Por Pegge, Sjoert A. H., Steens, Stefan C. A., Kunst, Henricus P. M., Meijer, Frederick J. A.
Publicado no Curr Radiol Rep (2017)

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

Por Blom, Stephanie S. A. H., Aarts, Henk, Wever, Capi C., Kunst, Henricus P. M., Semin, Gün R.
Publicado no Laryngoscope Investig Otolaryngol (2020)

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

Por Blom, Stephanie S. A. H., Aarts, Henk, Kunst, Henricus P. M., Wever, Capi C., Semin, Gün R.
Publicado no Brain Behav (2020)

What determines quality of life in patients with vestibular schwannoma?

Por Pruijn, Ineke M. J., Kievit, Wietske, Hentschel, Mayke A., Mulder, Jef J. S., Kunst, Henricus P. M.
Publicado no Clin Otolaryngol (2020)

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

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

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

Por Hentschel, Mayke A., Hannink, Gerjon, Steens, Stefan C. A., Mulder, Jef J. S., Rovers, Maroeska M., Kunst, Henricus P. M.
Publicado no Clin Otolaryngol (2020)

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

Por Vijverberg, Maarten A., Verhamme, Luc, van de Pol, Pascal, Kunst, Henricus P. M., Mylanus, Emmanuel A. M., Hol, Myrthe K. S.
Publicado no Eur Arch Otorhinolaryngol (2019)

Clinical relevance of occipital condyle fractures

Por van der Burg, Stijn J, Pouw, Martin H, Brink, Monique, Dekker, Helena, Kunst, Henricus P M, Hosman, Allard J F
Publicado no J Craniovertebr Junction Spine (2020)

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

Por Scholte, Mirre, Hentschel, Mayke A., Hannink, Gerjon, Kunst, Henricus P. M., Steens, Stefan C., Rovers, Maroeska M., Grutters, Janneke P. C.
Publicado no Clin Otolaryngol (2019)

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

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

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

Por 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.
Publicado em 2010

Paediatric Cochlear Implantation in Patients with Waardenburg Syndrome

Por 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.
Publicado no Audiol Neurootol (2016)

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

Por 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
Publicado em 2010

Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome

Por 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.
Publicado no 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

Por 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
Publicado em 2011

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

Por 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.
Publicado em 2011

Similar phenotypes caused by mutations in OTOG and OTOGL

Por 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.
Publicado em 2014

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

Por 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.
Publicado no Hum Mol Genet (2001)

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

Por 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
Publicado em 2010