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Manuela Neumann

Showing results (151-160 of 175) with videos related to

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Acta Neuropathologica|June 21, 2007
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar DegenerationNigel J Cairns, Eileen H Bigio, Ian R A Mackenzie, et al.
The Lancet. Neurology|April 9, 2008
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysisVivianna M Van Deerlin, James B Leverenz, Lynn M Bekris, et al.
Archives of Neurology|February 10, 2010
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegenerationChang-En Yu, Thomas D Bird, Lynn M Bekris, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 25, 2014
Erratum to: Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortiumIrina Alafuzoff, Maria Pikkarainen, Manuela Neumann, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 21, 2014
Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortiumIrina Alafuzoff, Maria Pikkarainen, Manuela Neumann, et al.
Neurobiology of Aging|July 31, 2012
Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotypeNicola J Rutherford, Michael G Heckman, Mariely Dejesus-Hernandez, et al.
Brain Pathology (Zurich, Switzerland)|September 25, 2018
Childhood supratentorial ependymomas with YAP1-MAMLD1 fusion: an entity with characteristic clinical, radiological, cytogenetic and histopathological featuresFelipe Andreiuolo, Pascale Varlet, Arnault Tauziède-Espariat, et al.
Neurobiology of Aging|May 29, 2014
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriersMarka van Blitterswijk, Bianca Mullen, Michael G Heckman, et al.
Molecular Neurodegeneration|September 21, 2014
Genetic modifiers in carriers of repeat expansions in the C9ORF72 geneMarka van Blitterswijk, Bianca Mullen, Aleksandra Wojtas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 3, 2024
Biomarker-Based Approach to α-Synucleinopathies: Lessons from NeuropathologyGabor G Kovacs, Lea T Grinberg, Glenda Halliday, et al.
Pageof 18

Showing results (151-160 of 175) with videos related to

Sort By:
Pageof 18
Acta Neuropathologica|June 21, 2007
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar DegenerationNigel J Cairns, Eileen H Bigio, Ian R A Mackenzie, et al.
The Lancet. Neurology|April 9, 2008
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysisVivianna M Van Deerlin, James B Leverenz, Lynn M Bekris, et al.
Archives of Neurology|February 10, 2010
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegenerationChang-En Yu, Thomas D Bird, Lynn M Bekris, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 25, 2014
Erratum to: Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortiumIrina Alafuzoff, Maria Pikkarainen, Manuela Neumann, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 21, 2014
Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortiumIrina Alafuzoff, Maria Pikkarainen, Manuela Neumann, et al.
Neurobiology of Aging|July 31, 2012
Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotypeNicola J Rutherford, Michael G Heckman, Mariely Dejesus-Hernandez, et al.
Brain Pathology (Zurich, Switzerland)|September 25, 2018
Childhood supratentorial ependymomas with YAP1-MAMLD1 fusion: an entity with characteristic clinical, radiological, cytogenetic and histopathological featuresFelipe Andreiuolo, Pascale Varlet, Arnault Tauziède-Espariat, et al.
Neurobiology of Aging|May 29, 2014
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriersMarka van Blitterswijk, Bianca Mullen, Michael G Heckman, et al.
Molecular Neurodegeneration|September 21, 2014
Genetic modifiers in carriers of repeat expansions in the C9ORF72 geneMarka van Blitterswijk, Bianca Mullen, Aleksandra Wojtas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 3, 2024
Biomarker-Based Approach to α-Synucleinopathies: Lessons from NeuropathologyGabor G Kovacs, Lea T Grinberg, Glenda Halliday, et al.
Pageof 18