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S Brandner

Showing results (71-80 of 95) with videos related to

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Neuromuscular Disorders : NMD|June 12, 2017
Deletion of P2 promoter of GJB1 gene a cause of Charcot-Marie-Tooth diseaseR Kulshrestha, S Burton-Jones, T Antoniadi, et al.
Oncogene|August 30, 2001
Germline SDHD mutation in paraganglioma of the spinal cordJ Masuoka, S Brandner, W Paulus, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replicationA J Raeber, A Sailer, I Hegyi, et al.
Gut|June 10, 2006
Prion infectivity in variant Creutzfeldt-Jakob disease rectumJ D F Wadsworth, S Joiner, K Fox, et al.
AJNR. American Journal of Neuroradiology|January 8, 2021
Regional and Volumetric Parameters for Diffusion-Weighted WHO Grade II and III Glioma Genotyping: A Method ComparisonS C Thust, J A Maynard, M Benenati, et al.
Neuromuscular Disorders : NMD|October 16, 2007
147th ENMC international workshop: guideline on processing and evaluation of sural nerve biopsies, 15-17 December 2006, Naarden, The NetherlandsC Sommer, S Brandner, P J Dyck, et al.
Acta Neurochirurgica|January 31, 2020
In vitro performance of combinations of anti-siphon devices with differential pressure valves in relation to the spatial positionI Fiss, M Vanderheyden, C von der Brelie, et al.
Annals of the New York Academy of Sciences|January 17, 1996
Mice homozygous for a modified beta-amyloid precursor protein (beta APP) gene show impaired behavior and high incidence of agenesis of the corpus callosumU Müller, N Cristina, Z W Li, et al.
Cell|December 2, 1994
Behavioral and anatomical deficits in mice homozygous for a modified beta-amyloid precursor protein geneU Müller, N Cristina, Z W Li, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1995
Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytomaJ A Kraus, J Koopmann, P Kaskel, et al.
Pageof 10

Showing results (71-80 of 95) with videos related to

Sort By:
Pageof 10
Neuromuscular Disorders : NMD|June 12, 2017
Deletion of P2 promoter of GJB1 gene a cause of Charcot-Marie-Tooth diseaseR Kulshrestha, S Burton-Jones, T Antoniadi, et al.
Oncogene|August 30, 2001
Germline SDHD mutation in paraganglioma of the spinal cordJ Masuoka, S Brandner, W Paulus, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replicationA J Raeber, A Sailer, I Hegyi, et al.
Gut|June 10, 2006
Prion infectivity in variant Creutzfeldt-Jakob disease rectumJ D F Wadsworth, S Joiner, K Fox, et al.
AJNR. American Journal of Neuroradiology|January 8, 2021
Regional and Volumetric Parameters for Diffusion-Weighted WHO Grade II and III Glioma Genotyping: A Method ComparisonS C Thust, J A Maynard, M Benenati, et al.
Neuromuscular Disorders : NMD|October 16, 2007
147th ENMC international workshop: guideline on processing and evaluation of sural nerve biopsies, 15-17 December 2006, Naarden, The NetherlandsC Sommer, S Brandner, P J Dyck, et al.
Acta Neurochirurgica|January 31, 2020
In vitro performance of combinations of anti-siphon devices with differential pressure valves in relation to the spatial positionI Fiss, M Vanderheyden, C von der Brelie, et al.
Annals of the New York Academy of Sciences|January 17, 1996
Mice homozygous for a modified beta-amyloid precursor protein (beta APP) gene show impaired behavior and high incidence of agenesis of the corpus callosumU Müller, N Cristina, Z W Li, et al.
Cell|December 2, 1994
Behavioral and anatomical deficits in mice homozygous for a modified beta-amyloid precursor protein geneU Müller, N Cristina, Z W Li, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1995
Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytomaJ A Kraus, J Koopmann, P Kaskel, et al.
Pageof 10