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R H Boerman

Showing results (21-30 of 31) with videos related to

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Journal of Neuro-Oncology|January 5, 2000
Suramin treatment of human glioma xenografts; effects on tumor vasculature and oxygenation statusH J Bernsen, P F Rijken, J P Peters, et al.
Journal of Neuro-Oncology|June 2, 2001
The relationship between genetic aberrations as detected by comparative genomic hybridization and vascularization in glioblastoma xenograftsH J Gilhuis, H J Bernse, J W Jeuken, et al.
Clinical Neurology and Neurosurgery|January 13, 2001
Comparative genomic hybridization of medulloblastomas and clinical relevance: eleven new cases and a review of the literatureH J Gilhuis, K L Anderl, R H Boerman, et al.
Archives of Neurology|June 1, 1995
Molecular genetic reevaluation of the Dutch hyperekplexia familyM A Tijssen, R Shiang, J van Deutekom, et al.
Journal of Virological Methods|August 1, 1989
Polymerase chain reaction and viral culture techniques to detect HSV in small volumes of cerebrospinal fluid; an experimental mouse encephalitis studyR H Boerman, E P Arnoldus, A K Raap, et al.
Journal of Neuropathology and Experimental Neurology|June 22, 1999
Identification of subgroups of high-grade oligodendroglial tumors by comparative genomic hybridizationJ W Jeuken, S H Sprenger, P Wesseling, et al.
Journal of Neuropathology and Experimental Neurology|September 1, 1996
The glial and mesenchymal elements of gliosarcomas share similar genetic alterationsR H Boerman, K Anderl, J Herath, et al.
Journal of Neuro-Oncology|March 16, 2004
Inverse correlation between genetic aberrations and malignancy grade in ependymal tumors: a paradox?H J Gilhuis, J van der Laak, P Wesseling, et al.
Journal of Neurosurgery|April 13, 2000
Genetic reflection of glioblastoma biopsy material in xenografts: characterization of 11 glioblastoma xenograft lines by comparative genomic hybridizationJ W Jeuken, S H Sprenger, P Wesseling, et al.
Journal of Medical Genetics|January 1, 1995
Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysisR H Boerman, R A Ophoff, T P Links, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Journal of Neuro-Oncology|January 5, 2000
Suramin treatment of human glioma xenografts; effects on tumor vasculature and oxygenation statusH J Bernsen, P F Rijken, J P Peters, et al.
Journal of Neuro-Oncology|June 2, 2001
The relationship between genetic aberrations as detected by comparative genomic hybridization and vascularization in glioblastoma xenograftsH J Gilhuis, H J Bernse, J W Jeuken, et al.
Clinical Neurology and Neurosurgery|January 13, 2001
Comparative genomic hybridization of medulloblastomas and clinical relevance: eleven new cases and a review of the literatureH J Gilhuis, K L Anderl, R H Boerman, et al.
Archives of Neurology|June 1, 1995
Molecular genetic reevaluation of the Dutch hyperekplexia familyM A Tijssen, R Shiang, J van Deutekom, et al.
Journal of Virological Methods|August 1, 1989
Polymerase chain reaction and viral culture techniques to detect HSV in small volumes of cerebrospinal fluid; an experimental mouse encephalitis studyR H Boerman, E P Arnoldus, A K Raap, et al.
Journal of Neuropathology and Experimental Neurology|June 22, 1999
Identification of subgroups of high-grade oligodendroglial tumors by comparative genomic hybridizationJ W Jeuken, S H Sprenger, P Wesseling, et al.
Journal of Neuropathology and Experimental Neurology|September 1, 1996
The glial and mesenchymal elements of gliosarcomas share similar genetic alterationsR H Boerman, K Anderl, J Herath, et al.
Journal of Neuro-Oncology|March 16, 2004
Inverse correlation between genetic aberrations and malignancy grade in ependymal tumors: a paradox?H J Gilhuis, J van der Laak, P Wesseling, et al.
Journal of Neurosurgery|April 13, 2000
Genetic reflection of glioblastoma biopsy material in xenografts: characterization of 11 glioblastoma xenograft lines by comparative genomic hybridizationJ W Jeuken, S H Sprenger, P Wesseling, et al.
Journal of Medical Genetics|January 1, 1995
Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysisR H Boerman, R A Ophoff, T P Links, et al.
Pageof 4