-
1
-
-
0000168230
-
Von Hippel-Lindau disease and capillary haemangioblastoma
-
Kleihues P., and Cavenee W.K. (Eds), WHO, Lyon
-
Bohling T., Plate K.H., Haltia M.J., Alitalo K., and Neumann H.P.H. Von Hippel-Lindau disease and capillary haemangioblastoma. In: Kleihues P., and Cavenee W.K. (Eds). Pathology & Genetics. Tumours of the nervous system (2000), WHO, Lyon 223-226
-
(2000)
Pathology & Genetics. Tumours of the nervous system
, pp. 223-226
-
-
Bohling, T.1
Plate, K.H.2
Haltia, M.J.3
Alitalo, K.4
Neumann, H.P.H.5
-
2
-
-
0035349415
-
Characteristic chromosomal aberrations in sporadic cerebellar hemangioblastomas revealed by comparative genomic hybridization
-
Sprenger S.H., Gijtenbeek J.M., Wesseling P., et al. Characteristic chromosomal aberrations in sporadic cerebellar hemangioblastomas revealed by comparative genomic hybridization. J Neurooncol 52 (2001) 241-247
-
(2001)
J Neurooncol
, vol.52
, pp. 241-247
-
-
Sprenger, S.H.1
Gijtenbeek, J.M.2
Wesseling, P.3
-
3
-
-
0036800998
-
Analysis of von Hippel-Lindau mutations with comparative genomic hybridization in sporadic and hereditary hemangioblastomas: possible genetic heterogeneity
-
Gijtenbeek J.M., Jacobs B., Sprenger S.H., et al. Analysis of von Hippel-Lindau mutations with comparative genomic hybridization in sporadic and hereditary hemangioblastomas: possible genetic heterogeneity. J Neurosurg 97 (2002) 977-982
-
(2002)
J Neurosurg
, vol.97
, pp. 977-982
-
-
Gijtenbeek, J.M.1
Jacobs, B.2
Sprenger, S.H.3
-
4
-
-
27944507362
-
Cellular and reticular variants of haemangioblastoma revisited: a clinicopathologic study of 88 cases
-
Hasselblatt M., Jeibmann A., Gerss J., et al. Cellular and reticular variants of haemangioblastoma revisited: a clinicopathologic study of 88 cases. Neuropathol Appl Neurobiol 31 (2005) 618-622
-
(2005)
Neuropathol Appl Neurobiol
, vol.31
, pp. 618-622
-
-
Hasselblatt, M.1
Jeibmann, A.2
Gerss, J.3
-
5
-
-
0001119370
-
Tumors of vascular origin
-
Bigner D.D., McLendon R.E., and Bruner J.M. (Eds), Arnold, London
-
Bruner J.M., Tien R.D., and McLendon R.E. Tumors of vascular origin. In: Bigner D.D., McLendon R.E., and Bruner J.M. (Eds). Russel and Rubinstein's pathology of tumors of the nervous system. 6th ed. (1998), Arnold, London 239-256
-
(1998)
Russel and Rubinstein's pathology of tumors of the nervous system. 6th ed.
, pp. 239-256
-
-
Bruner, J.M.1
Tien, R.D.2
McLendon, R.E.3
-
6
-
-
2442715146
-
Comparative genomic hybridization in central and peripheral nervous system tumors of childhood and adolescence
-
Rickert C.H., and Paulus W. Comparative genomic hybridization in central and peripheral nervous system tumors of childhood and adolescence. J Neuropathol Exp Neurol 63 (2004) 399-417
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, pp. 399-417
-
-
Rickert, C.H.1
Paulus, W.2
-
7
-
-
4444383870
-
Loss of heterozygosity reveals non-VHL allelic loss in hemangioblastomas at 22q13
-
Beckner M.E., Sasatomi E., Swalsky P.A., Hamilton R.L., Pollack I.F., and Finkelstein S.D. Loss of heterozygosity reveals non-VHL allelic loss in hemangioblastomas at 22q13. Hum Pathol 35 (2004) 1105-1111
-
(2004)
Hum Pathol
, vol.35
, pp. 1105-1111
-
-
Beckner, M.E.1
Sasatomi, E.2
Swalsky, P.A.3
Hamilton, R.L.4
Pollack, I.F.5
Finkelstein, S.D.6
-
8
-
-
0036211802
-
Recurrent DNA sequence copy losses on chromosomal arm 6q in capillary hemangioblastoma
-
Lemeta S., Aalto Y., Niemela M., et al. Recurrent DNA sequence copy losses on chromosomal arm 6q in capillary hemangioblastoma. Cancer Genet Cytogenet 133 (2002) 174-178
-
(2002)
Cancer Genet Cytogenet
, vol.133
, pp. 174-178
-
-
Lemeta, S.1
Aalto, Y.2
Niemela, M.3
-
9
-
-
5644246051
-
Loss of heterozygosity at 6q is frequent and concurrent with 3p loss in sporadic and familial capillary hemangioblastomas
-
Lemeta S., Pylkkanen L., Sainio M., et al. Loss of heterozygosity at 6q is frequent and concurrent with 3p loss in sporadic and familial capillary hemangioblastomas. J Neuropathol Exp Neurol 63 (2004) 1072-1079
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, pp. 1072-1079
-
-
Lemeta, S.1
Pylkkanen, L.2
Sainio, M.3
-
10
-
-
33745210767
-
Chromosomal imbalances in clear cell ependymomas
-
[in press]
-
Rickert C.H., Korshunov A., and Paulus W. Chromosomal imbalances in clear cell ependymomas. Mod Pathol (2006) [in press]
-
(2006)
Mod Pathol
-
-
Rickert, C.H.1
Korshunov, A.2
Paulus, W.3
-
11
-
-
2942559003
-
Chromosome imbalances in oligodendroglial tumors detected by comparative genomic hybridization
-
Bourdon V., Plessis G., Chapon F., Guarnieri J., Derlon J.M., and Jonveaux P. Chromosome imbalances in oligodendroglial tumors detected by comparative genomic hybridization. Ann Genet 47 (2004) 105-111
-
(2004)
Ann Genet
, vol.47
, pp. 105-111
-
-
Bourdon, V.1
Plessis, G.2
Chapon, F.3
Guarnieri, J.4
Derlon, J.M.5
Jonveaux, P.6
-
12
-
-
0033948113
-
Detection of chromosomal imbalances in central neurocytomas by using comparative genomic hybridization
-
Yin X.L., Pang J.C., Hui A.B., and Ng H.K. Detection of chromosomal imbalances in central neurocytomas by using comparative genomic hybridization. J Neurosurg 93 (2000) 77-81
-
(2000)
J Neurosurg
, vol.93
, pp. 77-81
-
-
Yin, X.L.1
Pang, J.C.2
Hui, A.B.3
Ng, H.K.4
-
13
-
-
3242739369
-
Value and limits of immunohistochemistry in differential diagnosis of clear cell primary brain tumors
-
Koperek O., Gelpi E., Birner P., Haberler C., Budka H., and Hainfellner J.A. Value and limits of immunohistochemistry in differential diagnosis of clear cell primary brain tumors. Acta Neuropathol 108 (2004) 24-30
-
(2004)
Acta Neuropathol
, vol.108
, pp. 24-30
-
-
Koperek, O.1
Gelpi, E.2
Birner, P.3
Haberler, C.4
Budka, H.5
Hainfellner, J.A.6
-
14
-
-
21344464959
-
D2-40, a novel monoclonal antibody against the M2A antigen as a marker to distinguish hemangioblastomas from renal cell carcinomas
-
Roy S., Chu A., Trojanowski J.Q., and Zhang P.J. D2-40, a novel monoclonal antibody against the M2A antigen as a marker to distinguish hemangioblastomas from renal cell carcinomas. Acta Neuropathol 109 (2005) 497-502
-
(2005)
Acta Neuropathol
, vol.109
, pp. 497-502
-
-
Roy, S.1
Chu, A.2
Trojanowski, J.Q.3
Zhang, P.J.4
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