A. Mey

发表

Mutations affecting BRAF, EGFR, PIK3CA, and KRAS are not associated with sporadic vestibular schwannomas

A. Cleton-Jansen, P. Hogendoorn, M. Malessy, 2013, Virchows Archiv.

High prevalence of occult paragangliomas in asymptomatic carriers of SDHD and SDHB gene mutations

J. Hamming, C. Tops, E. Corssmit, 2012, European Journal of Human Genetics.

Gene (cid:415) c and clinical characteris (cid:415) cs of Dutch paraganglioma pa (cid:415) ents

P. Devilee, J. Romijn, C. Tops, 2012 .

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families

E. Jordanova, P. Devilee, P. Taschner, 2004, Oncogene.

The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family

P. Devilee, C. Cornelisse, J. Oosterwijk, 2010, European Journal of Human Genetics.

The Respiratory Response to Carbon Dioxide in Humans with Unilateral and Bilateral Resections of the Carotid Bodies

Albert Dahan, M. Fatemian, P. Robbins, 2003, The Journal of physiology.

Confinement of PGL, an Imprinted Gene Causing Hereditary Paragangliomas, to a 2-cM Interval on 11q22–q23 and Exclusion of DRD2 and NCAM as Candidate Genes

J. Weissenbach, P. Devilee, C. Cornelisse, 1996, European journal of human genetics : EJHG.

Further Localization of the Gene for Hereditary Paragangliomas and Evidence for Linkage in Unrelated Families

P. Devilee, P. Heutink, B. Oostra, 1994, European journal of human genetics : EJHG.

Measurement of head and neck paragangliomas: is volumetric analysis worth the effort? A method comparison study

E. Corssmit, B. Verbist, F. Hes, 2016, Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery.

Validating the Penn Acoustic Neuroma Quality-of-Life Scale in Dutch Patients with Recently Diagnosed Vestibular Schwannoma

A. Kaptein, J. Jansen, A. Mey, 2012 .

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.

B. Devlin, W. Rubinstein, P. Devilee, 2000, Science.

Clinical infections and nonsurgical treatment of parapharyngeal space infections complicating throat infection.

A. V. D. van der Mey, G. Meerdink, J. V. D. van der Meer, 1989, Reviews of infectious diseases.

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.

J. Weber, P. Devilee, P. Heutink, 1992, Human molecular genetics.

Sensorineural hearing loss in adult onset Still's disease.

A. V. D. van der Mey, K. Heering, H. M. Markusse, 1988, Annals of the rheumatic diseases.

Management of carotid body tumors.

A. V. D. van der Mey, J. Jansen, J. V. van Baalen, 2001, Otolaryngologic clinics of North America.

Paragangliomas of the head and neck region show complete loss of heterozygosity at 11q22-q23 in chief cells and the flow-sorted DNA aneuploid fraction.

P. Devilee, M. Beekman, C. Cornelisse, 1998, Human pathology.

High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands

P. Devilee, E. Corssmit, C. Cornelisse, 2012, Clinical genetics.