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T Revesz

Showing results (91-100 of 135) with videos related to

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FEBS Letters|November 19, 2002
The complex relationship between soluble and insoluble tau in tauopathies revealed by efficient dephosphorylation and specific antibodiesD P Hanger, G M Gibb, R de Silva, et al.
Brain Pathology (Zurich, Switzerland)|April 15, 2006
Genetic alterations of the BRI2 gene: familial British and Danish dementiasJ Ghiso, A Rostagno, Y Tomidokoro, et al.
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 11P Giunti, H Houlden, C Gardner-Thorpe, et al.
Neuropathology and Applied Neurobiology|August 13, 2004
Frontotemporal lobar degeneration and ubiquitin immunohistochemistryK A Josephs, J L Holton, M N Rossor, et al.
Brain : a Journal of Neurology|April 4, 2008
Clinical outcomes of progressive supranuclear palsy and multiple system atrophyS S O'Sullivan, L A Massey, D R Williams, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 19, 2004
Pathological substrate for regional distribution of increased atrophy rates in progressive supranuclear palsyD C Paviour, J M Schott, J M Stevens, et al.
Neurology|September 26, 1997
11C-flumazenil PET, volumetric MRI, and quantitative pathology in mesial temporal lobe epilepsyM J Koepp, M P Richardson, C Labbé, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 26, 2000
A decamer duplication in the 3' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindredR Vidal, T Revesz, A Rostagno, et al.
Leukemia|June 11, 2010
Bone marrow fibrosis and vascular density lack prognostic significance in childhood acute lymphoblastic leukaemiaA Bharos, A-J de Jong, N Manton, et al.
British Journal of Pharmacology|October 6, 1997
Central benzodiazepine receptor autoradiography in hippocampal sclerosisK S Hand, V H Baird, W Van Paesschen, et al.
Pageof 14

Showing results (91-100 of 135) with videos related to

Sort By:
Pageof 14
FEBS Letters|November 19, 2002
The complex relationship between soluble and insoluble tau in tauopathies revealed by efficient dephosphorylation and specific antibodiesD P Hanger, G M Gibb, R de Silva, et al.
Brain Pathology (Zurich, Switzerland)|April 15, 2006
Genetic alterations of the BRI2 gene: familial British and Danish dementiasJ Ghiso, A Rostagno, Y Tomidokoro, et al.
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 11P Giunti, H Houlden, C Gardner-Thorpe, et al.
Neuropathology and Applied Neurobiology|August 13, 2004
Frontotemporal lobar degeneration and ubiquitin immunohistochemistryK A Josephs, J L Holton, M N Rossor, et al.
Brain : a Journal of Neurology|April 4, 2008
Clinical outcomes of progressive supranuclear palsy and multiple system atrophyS S O'Sullivan, L A Massey, D R Williams, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 19, 2004
Pathological substrate for regional distribution of increased atrophy rates in progressive supranuclear palsyD C Paviour, J M Schott, J M Stevens, et al.
Neurology|September 26, 1997
11C-flumazenil PET, volumetric MRI, and quantitative pathology in mesial temporal lobe epilepsyM J Koepp, M P Richardson, C Labbé, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 26, 2000
A decamer duplication in the 3' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindredR Vidal, T Revesz, A Rostagno, et al.
Leukemia|June 11, 2010
Bone marrow fibrosis and vascular density lack prognostic significance in childhood acute lymphoblastic leukaemiaA Bharos, A-J de Jong, N Manton, et al.
British Journal of Pharmacology|October 6, 1997
Central benzodiazepine receptor autoradiography in hippocampal sclerosisK S Hand, V H Baird, W Van Paesschen, et al.
Pageof 14