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T Ströbel

Showing results (1-10 of 13) with videos related to

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Clinical Neuropathology|December 24, 2010
Unclassifiable tauopathy associated with an A152T variation in MAPT exon 7G G Kovacs, A Wöhrer, T Ströbel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2006
Alzheimer-type neuropathology in a 28 year old patient with iatrogenic Creutzfeldt-Jakob disease after dural graftingM Preusser, T Ströbel, E Gelpi, et al.
Cancer Gene Therapy|December 17, 2016
Extracellular vesicle-mediated suicide mRNA/protein delivery inhibits glioblastoma tumor growth in vivoE P Erkan, D Senfter, S Madlener, et al.
Clinical Genetics|January 11, 2016
The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNAH Cetin, A Wöhrer, I Rittelmeyer, et al.
Oncogene|October 30, 2013
Depletion of minichromosome maintenance protein 7 inhibits glioblastoma multiforme tumor growth in vivoE P Erkan, T Ströbel, G Lewandrowski, et al.
Journal of Neuropathology and Experimental Neurology|May 31, 2001
Fibroblasts can express glial fibrillary acidic protein (GFAP) in vivoJ A Hainfellner, T Voigtländer, T Ströbel, et al.
Neuropathology and Applied Neurobiology|November 16, 2004
Presence of D110 antigen expressing immunocompetent cells in glioblastoma associates with prolonged survivalM Preusser, T Ströbel, P Birner, et al.
European Journal of Cancer (Oxford, England : 1990)|January 31, 2002
DNA topoisomerase IIalpha expression in optic pathway gliomas of childhoodM Bredel, I Slavc, P Birner, et al.
Neurology|November 23, 2005
Increased incidence of genetic human prion disease in HungaryG G Kovács, L László, A Bakos, et al.
Clinical Neuropathology|October 9, 2002
Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literatureJ Wanschit, S Nakano, B Goudeau, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Clinical Neuropathology|December 24, 2010
Unclassifiable tauopathy associated with an A152T variation in MAPT exon 7G G Kovacs, A Wöhrer, T Ströbel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2006
Alzheimer-type neuropathology in a 28 year old patient with iatrogenic Creutzfeldt-Jakob disease after dural graftingM Preusser, T Ströbel, E Gelpi, et al.
Cancer Gene Therapy|December 17, 2016
Extracellular vesicle-mediated suicide mRNA/protein delivery inhibits glioblastoma tumor growth in vivoE P Erkan, D Senfter, S Madlener, et al.
Clinical Genetics|January 11, 2016
The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNAH Cetin, A Wöhrer, I Rittelmeyer, et al.
Oncogene|October 30, 2013
Depletion of minichromosome maintenance protein 7 inhibits glioblastoma multiforme tumor growth in vivoE P Erkan, T Ströbel, G Lewandrowski, et al.
Journal of Neuropathology and Experimental Neurology|May 31, 2001
Fibroblasts can express glial fibrillary acidic protein (GFAP) in vivoJ A Hainfellner, T Voigtländer, T Ströbel, et al.
Neuropathology and Applied Neurobiology|November 16, 2004
Presence of D110 antigen expressing immunocompetent cells in glioblastoma associates with prolonged survivalM Preusser, T Ströbel, P Birner, et al.
European Journal of Cancer (Oxford, England : 1990)|January 31, 2002
DNA topoisomerase IIalpha expression in optic pathway gliomas of childhoodM Bredel, I Slavc, P Birner, et al.
Neurology|November 23, 2005
Increased incidence of genetic human prion disease in HungaryG G Kovács, L László, A Bakos, et al.
Clinical Neuropathology|October 9, 2002
Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literatureJ Wanschit, S Nakano, B Goudeau, et al.
Pageof 2