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J C Jansen

Showing results (21-30 of 56) with videos related to

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Journal of Medical Genetics|July 6, 2004
The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical featuresR F Badenhop, J C Jansen, P A Fagan, et al.
Leukemia|April 22, 2005
Identification of e19a2 BCR-ABL fusions (mu-BCR breakpoints) at the DNA level by ligation-mediated PCRN Boeckx, M W J C Jansen, C Haskovec, et al.
Leukemia|April 6, 2007
Complex MLL rearrangements in t(4;11) leukemia patients with absent AF4.MLL fusion alleleE Kowarz, T Burmeister, L Lo Nigro, et al.
The Journal of Clinical Endocrinology and Metabolism|January 18, 2007
Malignant paragangliomas associated with mutations in the succinate dehydrogenase D geneB Havekes, E P M Corssmit, J C Jansen, et al.
Genes and Immunity|April 16, 2004
Interleukin 10-2849AA genotype protects against pre-eclampsiaC J M de Groot, M W J C Jansen, R M Bertina, et al.
Pediatric Blood & Cancer|February 18, 2004
Acute lymphoblastic leukemia followed by a clonally-unrelated EBV-positive non-Hodgkin lymphoma and a clonally-related myelomonocytic leukemia cutisTomasz Szczepański, Gerard A M de Vaan, Auke Beishuizen, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|October 11, 2015
Measurement of head and neck paragangliomas: is volumetric analysis worth the effort? A method comparison studyB L Heesterman, B M Verbist, A G L van der Mey, et al.
Journal of Medical Genetics|May 1, 1996
First experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas)J C Oosterwijk, J C Jansen, E M van Schothorst, et al.
European Journal of Endocrinology|May 4, 2010
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 symptomsN van Duinen, D Steenvoorden, B A Bonsing, et al.
European Journal of Endocrinology|February 9, 2013
Quality of life is decreased in patients with paragangliomasL T van Hulsteijn, A Louisse, B Havekes, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|July 6, 2004
The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical featuresR F Badenhop, J C Jansen, P A Fagan, et al.
Leukemia|April 22, 2005
Identification of e19a2 BCR-ABL fusions (mu-BCR breakpoints) at the DNA level by ligation-mediated PCRN Boeckx, M W J C Jansen, C Haskovec, et al.
Leukemia|April 6, 2007
Complex MLL rearrangements in t(4;11) leukemia patients with absent AF4.MLL fusion alleleE Kowarz, T Burmeister, L Lo Nigro, et al.
The Journal of Clinical Endocrinology and Metabolism|January 18, 2007
Malignant paragangliomas associated with mutations in the succinate dehydrogenase D geneB Havekes, E P M Corssmit, J C Jansen, et al.
Genes and Immunity|April 16, 2004
Interleukin 10-2849AA genotype protects against pre-eclampsiaC J M de Groot, M W J C Jansen, R M Bertina, et al.
Pediatric Blood & Cancer|February 18, 2004
Acute lymphoblastic leukemia followed by a clonally-unrelated EBV-positive non-Hodgkin lymphoma and a clonally-related myelomonocytic leukemia cutisTomasz Szczepański, Gerard A M de Vaan, Auke Beishuizen, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|October 11, 2015
Measurement of head and neck paragangliomas: is volumetric analysis worth the effort? A method comparison studyB L Heesterman, B M Verbist, A G L van der Mey, et al.
Journal of Medical Genetics|May 1, 1996
First experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas)J C Oosterwijk, J C Jansen, E M van Schothorst, et al.
European Journal of Endocrinology|May 4, 2010
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 symptomsN van Duinen, D Steenvoorden, B A Bonsing, et al.
European Journal of Endocrinology|February 9, 2013
Quality of life is decreased in patients with paragangliomasL T van Hulsteijn, A Louisse, B Havekes, et al.
Pageof 6