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The British Journal of Radiology
|
August 31, 2006
Disseminated mucormycosis in haematological patients: CT and MRI findings with pathological correlation
M Horger, H Hebart, H Schimmel, et al.
Neuropathology and Applied Neurobiology
|
July 5, 2013
BRAF V600E expression and distribution in desmoplastic infantile astrocytoma/ganglioglioma
C Koelsche, F Sahm, W Paulus, et al.
British Journal of Cancer
|
August 6, 2014
Head and neck cancer relapse after chemoradiotherapy correlates with CD163+ macrophages in primary tumour and CD11b+ myeloid cells in recurrences
P Balermpas, F Rödel, R Liberz, et al.
Neuropathology and Applied Neurobiology
|
March 18, 2005
Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2
U Rüb, D Del Turco, K Bürk, et al.
International Journal of Oncology
|
May 4, 2012
PAX2 is an antiapoptotic molecule with deregulated expression in medulloblastoma
M C Burger, D P Brucker, P Baumgarten, et al.
Oncogene
|
February 15, 2011
Bone morphogenetic protein-7 is a MYC target with prosurvival functions in childhood medulloblastoma
G Fiaschetti, D Castelletti, S Zoller, et al.
Neuropathology and Applied Neurobiology
|
May 12, 2007
De novo erythropoietin receptor (EPO-R) expression in human neoplastic glial cells decreases with grade of malignancy but is favourably associated with patient survival
M Mittelbronn, D Capper, B Bunz, et al.
Cell Death & Disease
|
May 18, 2013
Activation of executioner caspases is a predictor of progression-free survival in glioblastoma patients: a systems medicine approach
Á C Murphy, B Weyhenmeyer, J Schmid, et al.
Neurology
|
October 13, 2004
Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3
U Rüb, K Bürk, L Schöls, et al.
Neuropathology and Applied Neurobiology
|
October 15, 2013
Loss of FUBP1 expression in gliomas predicts FUBP1 mutation and is associated with oligodendroglial differentiation, IDH1 mutation and 1p/19q loss of heterozygosity
P Baumgarten, P N Harter, M Tönjes, et al.
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of 5
Search research articles
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Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
The British Journal of Radiology
|
August 31, 2006
Disseminated mucormycosis in haematological patients: CT and MRI findings with pathological correlation
M Horger, H Hebart, H Schimmel, et al.
Neuropathology and Applied Neurobiology
|
July 5, 2013
BRAF V600E expression and distribution in desmoplastic infantile astrocytoma/ganglioglioma
C Koelsche, F Sahm, W Paulus, et al.
British Journal of Cancer
|
August 6, 2014
Head and neck cancer relapse after chemoradiotherapy correlates with CD163+ macrophages in primary tumour and CD11b+ myeloid cells in recurrences
P Balermpas, F Rödel, R Liberz, et al.
Neuropathology and Applied Neurobiology
|
March 18, 2005
Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2
U Rüb, D Del Turco, K Bürk, et al.
International Journal of Oncology
|
May 4, 2012
PAX2 is an antiapoptotic molecule with deregulated expression in medulloblastoma
M C Burger, D P Brucker, P Baumgarten, et al.
Oncogene
|
February 15, 2011
Bone morphogenetic protein-7 is a MYC target with prosurvival functions in childhood medulloblastoma
G Fiaschetti, D Castelletti, S Zoller, et al.
Neuropathology and Applied Neurobiology
|
May 12, 2007
De novo erythropoietin receptor (EPO-R) expression in human neoplastic glial cells decreases with grade of malignancy but is favourably associated with patient survival
M Mittelbronn, D Capper, B Bunz, et al.
Cell Death & Disease
|
May 18, 2013
Activation of executioner caspases is a predictor of progression-free survival in glioblastoma patients: a systems medicine approach
Á C Murphy, B Weyhenmeyer, J Schmid, et al.
Neurology
|
October 13, 2004
Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3
U Rüb, K Bürk, L Schöls, et al.
Neuropathology and Applied Neurobiology
|
October 15, 2013
Loss of FUBP1 expression in gliomas predicts FUBP1 mutation and is associated with oligodendroglial differentiation, IDH1 mutation and 1p/19q loss of heterozygosity
P Baumgarten, P N Harter, M Tönjes, et al.
Page
of 5