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

nork Hendriks, Tom, Kunst, Henricus P. M., Huppelschoten, Maarten, Doorduin, Jonne, Ter Laan, Mark
Argitaratua izan da Acta Neurochir (Wien) (2020)

Pulsatile Tinnitus: Differential Diagnosis and Radiological Work-Up

nork Pegge, Sjoert A. H., Steens, Stefan C. A., Kunst, Henricus P. M., Meijer, Frederick J. A.
Argitaratua izan da Curr Radiol Rep (2017)

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

nork Blom, Stephanie S. A. H., Aarts, Henk, Wever, Capi C., Kunst, Henricus P. M., Semin, Gün R.
Argitaratua izan da Laryngoscope Investig Otolaryngol (2020)

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

nork Blom, Stephanie S. A. H., Aarts, Henk, Kunst, Henricus P. M., Wever, Capi C., Semin, Gün R.
Argitaratua izan da Brain Behav (2020)

What determines quality of life in patients with vestibular schwannoma?

nork Pruijn, Ineke M. J., Kievit, Wietske, Hentschel, Mayke A., Mulder, Jef J. S., Kunst, Henricus P. M.
Argitaratua izan da Clin Otolaryngol (2020)

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

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

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

nork Hentschel, Mayke A., Hannink, Gerjon, Steens, Stefan C. A., Mulder, Jef J. S., Rovers, Maroeska M., Kunst, Henricus P. M.
Argitaratua izan da Clin Otolaryngol (2020)

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

nork Vijverberg, Maarten A., Verhamme, Luc, van de Pol, Pascal, Kunst, Henricus P. M., Mylanus, Emmanuel A. M., Hol, Myrthe K. S.
Argitaratua izan da Eur Arch Otorhinolaryngol (2019)

Clinical relevance of occipital condyle fractures

nork van der Burg, Stijn J, Pouw, Martin H, Brink, Monique, Dekker, Helena, Kunst, Henricus P M, Hosman, Allard J F
Argitaratua izan da J Craniovertebr Junction Spine (2020)

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

nork Scholte, Mirre, Hentschel, Mayke A., Hannink, Gerjon, Kunst, Henricus P. M., Steens, Stefan C., Rovers, Maroeska M., Grutters, Janneke P. C.
Argitaratua izan da Clin Otolaryngol (2019)

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

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

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

nork 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.
Argitaratua 2010

Paediatric Cochlear Implantation in Patients with Waardenburg Syndrome

nork 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.
Argitaratua izan da Audiol Neurootol (2016)

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

nork 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
Argitaratua 2010

Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome

nork 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.
Argitaratua izan da 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

nork 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
Argitaratua 2011

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

nork 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.
Argitaratua 2011

Similar phenotypes caused by mutations in OTOG and OTOGL

nork 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.
Argitaratua 2014

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

nork 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.
Argitaratua izan da Hum Mol Genet (2001)

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

nork 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
Argitaratua 2010