Pathology and genetics of tumours of the nervous system.
By P. Kleihues, W. Cavenee. 2000
1,451 citations recorded by the source corpus.
View Paper: https://www.semanticscholar.org/paper/5bba2907282b09915b92dbce6a900d1b3975b117
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- H. Ohgaki
- P. Kleihues
- D. Louis
- S. Pollard
- M. Westphal
- H. Phillips
- N. Shinojima
- K. Yoshikawa
Citations in the corpus
- Molecular subclasses of high-grade glioma predict prognosis, delineate a pattern of disease progression, and resemble stages in neurogenesis. (2006, methodology): “Cases were graded according to WHO criteria (Kleihues and Cavenee, 2000; see Table S2), and sections from frozen tissues were examined by a neuropathologist (K.A.) to ensure that R90% of the sample represented tumor.”
- Prognostic value of epidermal growth factor receptor in patients with glioblastoma multiforme. (2003, methodology): “K. and Y. I.) according to criteria published by WHO (51, 52); tumors exhibiting prominent microvascular proliferation and/or necrosis, in addition to high cellularity, marked nuclear atypia, and remarkable mitotic activity were diagnosed as GBM.”
- Neurofibromas in NF1: Schwann Cell Origin and Role of Tumor Environment (2002, background): “More detailed histological analysis of cranial nerves and spinal nerve roots revealed that each mouse with this genotype had extensive proliferation of delicate, elongated, bipolar cells identical to those seen in human neurofibromas (14) (Fig.”
- Population-based studies on incidence, survival rates, and genetic alterations in astrocytic and oligodendroglial gliomas. (2005, methodology): “Histologic diagnoses were reevaluated according to the new WHO classification of tumors of the nervous system (9, 10).”
- Glioma stem cell lines expanded in adherent culture have tumor-specific phenotypes and are suitable for chemical and genetic screens. (2009, background): “Gliomas are classified as astrocytoma, oligodendroglioma, or ependymoma, based on the glial cell type that predominates in the tumor (Kleihues and Cavenee, 2000).”