J. Jansen

发表

Near-infrared fluorescence sentinel lymph node mapping of the oral cavity in head and neck cancer patients.

Cornelis J H van de Velde, Alexander L Vahrmeijer, John V Frangioni, 2013, Oral oncology.

Long-term voice outcomes of laryngeal framework surgery for unilateral vocal fold paralysis

B. Heijnen, J. Jansen, A. Langeveld, 2021, European Archives of Oto-Rhino-Laryngology.

Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum.

W. Dinjens, E. Korpershoek, E. Corssmit, 2015, The Journal of clinical endocrinology and metabolism.

Germline DLST variants promote epigenetic modifications in pheochromocytoma-paraganglioma.

P. Devilee, A. Gimenez-Roqueplo, J. Favier, 2020, Journal of Clinical Endocrinology and Metabolism.

Low penetrance of a SDHB mutation in a large Dutch paraganglioma family

H. Morreau, J. Romijn, M. Weiss, 2010, BMC Medical Genetics.

Emotional Intelligence in Association With Quality of Life in Patients Recently Diagnosed With Vestibular Schwannoma

H. Putter, A. V. D. van der Mey, A. Kaptein, 2014, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Two Immigrants with Tuberculosis of the Ear, Nose, and Throat Region with Skull Base and Cranial Nerve Involvement

R. Richardus, S. Steens, S. Arend, 2011, Case reports in medicine.

Estimation of growth rate in patients with head and neck paragangliomas influences the treatment proposal

A. V. D. van der Mey, J. Jansen, A. Zwinderman, 2000, Cancer.

Case of spontaneous regression of carotid body tumor in a SDHD mutant: a discussion on potential mechanisms based on a review of the literature

M. Kruit, F. Hes, J. Jansen, 2012, World Journal of Surgical Oncology.

First experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas).

P. Devilee, J. Oosterwijk, E. Bakker, 1996, Journal of medical genetics.

The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers

C. Leemans, H. Timmers, E. Corssmit, 2018, Clinical genetics.

Phenotype of SDHB mutation carriers in the Netherlands

C. Tops, E. Corssmit, F. Hes, 2014, Familial Cancer.

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 .

Muta (cid:415) on spectrum of the succinate dehydrogenase genes in the Netherlands

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

Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients

P. Devilee, J. Romijn, A. V. D. van der Mey, 2011, Clinical endocrinology.

Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene

P. Devilee, P. Taschner, C. Cornelisse, 2001, Genes, chromosomes & cancer.

Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomas.

J. Romijn, M. Weiss, A. V. D. van der Mey, 2009, Endocrine-Related Cancer.

Malignant paragangliomas associated with mutations in the succinate dehydrogenase D gene.

J. Romijn, A. V. D. van der Mey, E. Corssmit, 2007, The Journal of clinical endocrinology and metabolism.

Quality of Life in 807 Patients with Vestibular Schwannoma: Comparing Treatment Modalities

H. Putter, A. Stiggelbout, A. V. D. van der Mey, 2017, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Parent-of-origin tumorigenesis is mediated by an essential imprinted modifier in SDHD- linked paragangliomas: SLC22A18 and CDKN1C are candidate tumor modifiers

P. Devilee, C. Ruivenkamp, C. Ras, 2017 .

The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical features

P. Schofield, R. Badenhop, J. Jansen, 2004, Journal of Medical Genetics.

Founder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands.

P. Devilee, D. Prins, A. V. D. van der Mey, 1998, American journal of human genetics.

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.

Long-term in vitro 2D-culture of SDHB and SDHD-related human paragangliomas and pheochromocytomas

P. Devilee, E. Korpershoek, A. Schepers, 2022, PloS one.

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations

P. Devilee, W. Dinjens, E. Korpershoek, 2014, BMC Medical Genetics.

Phenotype of SDHB mutation carriers in the Netherlands

C. Tops, E. Corssmit, F. Hes, 2014, Familial Cancer.

No difference in phenotype of the main Dutch SDHD founder mutations

E. Corssmit, F. Hes, J. Jansen, 2013, Clinical endocrinology.

Long-Term Quality of Life of Vestibular Schwannoma Patients: A Longitudinal Analysis.

A. Stiggelbout, J. Jansen, E. Hensen, 2022, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

The impact of vestibular schwannoma and its management on employment

A. V. D. van der Mey, M. D. de Ridder, J. Jansen, 2021, European Archives of Oto-Rhino-Laryngology.

Pheochromocytomas detected by biochemical screening in predisposed subjects are associated with lower prevalence of clinical and biochemical manifestations and smaller tumors than pheochromocytomas detected by signs and symptoms.

J. Romijn, B. Bonsing, E. Corssmit, 2010, European journal of endocrinology.

Clinical progression and metachronous paragangliomas in a large cohort of SDHD germline variant carriers

A. V. D. van der Mey, E. Corssmit, Lisa M. H. de Pont, 2018, European Journal of Human Genetics.

Quality of life is decreased in patients with paragangliomas.

A. Kaptein, E. Corssmit, J. Smit, 2013, European journal of endocrinology.

Normal Life Expectancy for Paraganglioma Patients: A 50-Year-Old Cohort Revisited

A. V. D. van der Mey, E. Corssmit, F. Hes, 2011, Skull base : official journal of North American Skull Base Society ... [et al.].

Management of carotid body tumors.

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

Jugular and vagal paragangliomas: Systematic study of management with surgery and radiotherapy

W. Mendenhall, P. Strojan, C. Silver, 2013, Head & neck.

Nationwide study of patients with head and neck paragangliomas carrying SDHB germline mutations

C. Leemans, H. Timmers, E. Corssmit, 2018, BJS open.

Evaluation of subclasses for T4‐classified squamous cell carcinoma of the external auditory canal

C. R. Leemans, J. Bouček, B. F. van der Laan, 2022, Head & neck.

CD44 Expression Predicts Local Recurrence after Radiotherapy in Larynx Cancer

F. Hoebers, E. Schuuring, C. Rasch, 2010, Clinical Cancer Research.

EGFR and αvβ6 as Promising Targets for Molecular Imaging of Cutaneous and Mucosal Squamous Cell Carcinoma of the Head and Neck Region

A. Vahrmeijer, C. Sier, J. Jansen, 2020, Cancers.

Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients.

P. Devilee, S. Verhoef, M. Weiss, 2009, Endocrine-related cancer.

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma.

C. Cremers, P. de Knijff, P. Devilee, 2010, The Lancet. Oncology.

Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study

W. Dinjens, R. Oldenburg, C. Tops, 2018, The Journal of clinical endocrinology and metabolism.

Parent-of-origin tumourigenesis is mediated by an essential imprinted modifier in SDHD-linked paragangliomas: SLC22A18 and CDKN1C are candidate tumour modifiers.

P. Devilee, C. Ruivenkamp, C. Ras, 2016, Human molecular genetics.

Prognostic Factors for the Outcome of Translabyrinthine Surgery for Vestibular Schwannomas

S. Böhringer, A. V. D. van der Mey, M. Malessy, 2020, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

A prediction model for recurrence after translabyrinthine surgery for vestibular schwannoma: toward personalized postoperative surveillance

S. Böhringer, A. V. D. van der Mey, M. Malessy, 2022, European Archives of Oto-Rhino-Laryngology.

Mathematical Models for Tumor Growth and the Reduction of Overtreatment

A. V. D. van der Mey, E. Corssmit, Lisa M. H. de Pont, 2018, Journal of Neurological Surgery Part B: Skull Base.

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.

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

C. Cremers, H. Kremer, L. Hoefsloot, 2011, Clinical Cancer Research.

Regression and local control rates after radiotherapy for jugulotympanic paragangliomas: systematic review and meta-analysis.

O. Dekkers, E. Corssmit, J. A. Smit, 2013, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma

Peter Devilee, Edward Blair, Jean-Pierre Bayley, 2006, BMC Medical Genetics.

Chapter Penetrance and phenotype of the SDHD.D92Y muta (cid:415) on

P. Devilee, J. Oosterwijk, J. Jansen, 2012 .

The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients

P. Devilee, M. Losekoot, M. Weiss, 2009, BMC Medical Genetics.

Color Doppler imaging of paragangliomas in the neck

A. V. D. van der Mey, R. J. Baatenburg de Jong, J. Schipper, 1997, Journal of clinical ultrasound : JCU.

Increased Mortality in SDHB but Not in SDHD Pathogenic Variant Carriers

O. Dekkers, C. Leemans, H. Timmers, 2019, Cancers.

Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma–paraganglioma

P. Devilee, H. Neumann, D. Ascher, 2019, Journal of Medical Genetics.

The phenotype of SDHB germline mutation carriers: a nationwide study.

C. Leemans, C. Tops, H. Timmers, 2017, European journal of endocrinology.

Increased urinary excretion of 3-methoxytyramine in patients with head and neck paragangliomas.

J. Romijn, I. Kema, E. Corssmit, 2010, The Journal of clinical endocrinology and metabolism.

Age and Tumor Volume Predict Growth of Carotid and Vagal Body Paragangliomas

A. V. D. van der Mey, E. Corssmit, Lisa M. H. de Pont, 2017, Journal of Neurological Surgery Part B: Skull Base.

Reduced quality of life in patients with head-and-neck paragangliomas.

J. Romijn, A. V. D. van der Mey, E. Corssmit, 2008, European journal of endocrinology.

Management of vagal paraganglioma: is operative resection really the best option?

J. Jansen, J. Bradshaw, J. C. Jansen, 2005, Surgery.

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.

Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas.

P. Taschner, J. Romijn, M. Losekoot, 2005, European journal of endocrinology.

Effects of octreotide therapy in progressive head and neck paragangliomas: Case series

E. Corssmit, J. Smit, B. Verbist, 2013, Head & neck.

No evidence for increased mortality in SDHD variant carriers compared with the general population

O. Dekkers, E. Corssmit, F. Hes, 2015, European Journal of Human Genetics.

University of Groningen Increased Mortality in SDHB but Not in SDHD Pathogenic Variant Carriers Rijken

O. Dekkers, H. Timmers, E. Corssmit, 2019 .

Systemic and local human papillomavirus 16‐specific T‐cell immunity in patients with head and neck cancer

S. H. van der Burg, H. Gelderblom, V. Smit, 2012, International journal of cancer.

Recurrent Rhabdoid Meningioma: Case Report.

J. Sheehy, J. Jansen, P. Fagan, 2003, Skull base : official journal of North American Skull Base Society ... [et al.].

Validation of a gene expression signature for assessment of lymph node metastasis in oral squamous cell carcinoma.

Ed Schuuring, Frank K J Leusink, Paul Roepman, 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Carotid body tumors are not associated with an increased risk for sleep-disordered breathing

J. G. Dijk, J. Romijn, E. Corssmit, 2013, Sleep and Breathing.

Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas

E. Jordanova, P. Devilee, E. Korpershoek, 2017, Oncotarget.

Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants.

G. Wanna, J. Widimský, K. Pacak, 2023, The lancet. Diabetes & endocrinology.

Validating the Penn Acoustic Neuroma Quality of Life Scale in a Sample of Dutch Patients Recently Diagnosed With Vestibular Schwannoma

H. Putter, A. V. D. van der Mey, A. Kaptein, 2013, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

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

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

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

C. Leemans, N. Hanai, M. Wierzbicka, 2020, Head & neck.

Clinical progression and metachronous paragangliomas in a large cohort of SDHD germline variant carriers

A. V. D. van der Mey, E. Corssmit, Lisa M. H. de Pont, 2018, European Journal of Human Genetics.