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Parastoo Momeni

Showing results (21-30 of 47) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|August 4, 2005
Taiwanese cases of SCA2 are derived from a single founderParastoo Momeni, Chin-Song Lu, Yah-Huei Wu Chou, et al.
Neurobiology of Aging|April 3, 2013
Androgen receptor gene and sex-specific Alzheimer's diseaseRaffaele Ferrari, Saad Dawoodi, Merrill Raju, et al.
Brain : a Journal of Neurology|October 13, 2006
Novel splicing mutation in the progranulin gene causing familial corticobasal syndromeMario Masellis, Parastoo Momeni, Wendy Meschino, et al.
Neurobiology of Aging|September 28, 2011
FUS and TDP43 genetic variability in FTD and CBSEdward D Huey, Raffaele Ferrari, Jorge H Moreno, et al.
Neurobiology of Aging|February 8, 2014
Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsyRaffaele Ferrari, Mina Ryten, Roberto Simone, et al.
Annals of Neurology|September 20, 2006
Characteristics of frontotemporal dementia patients with a Progranulin mutationEdward D Huey, Jordan Grafman, Eric M Wassermann, et al.
Acta Neuropathologica|March 23, 2011
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS geneJulie S Snowden, Quan Hu, Sara Rollinson, et al.
Neurobiology of Aging|March 31, 2012
Screening for C9ORF72 repeat expansion in FTLDRaffaele Ferrari, Kin Mok, Jorge H Moreno, et al.
Acta Neuropathologica|October 28, 2010
Pathological correlates of frontotemporal lobar degeneration in the elderlyAtik Baborie, Timothy D Griffiths, Evelyn Jaros, et al.
Neuro-Degenerative Diseases|September 7, 2006
Genetic variability in CHMP2B and frontotemporal dementiaParastoo Momeni, Ekaterina Rogaeva, Vivianna Van Deerlin, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Movement Disorders : Official Journal of the Movement Disorder Society|August 4, 2005
Taiwanese cases of SCA2 are derived from a single founderParastoo Momeni, Chin-Song Lu, Yah-Huei Wu Chou, et al.
Neurobiology of Aging|April 3, 2013
Androgen receptor gene and sex-specific Alzheimer's diseaseRaffaele Ferrari, Saad Dawoodi, Merrill Raju, et al.
Brain : a Journal of Neurology|October 13, 2006
Novel splicing mutation in the progranulin gene causing familial corticobasal syndromeMario Masellis, Parastoo Momeni, Wendy Meschino, et al.
Neurobiology of Aging|September 28, 2011
FUS and TDP43 genetic variability in FTD and CBSEdward D Huey, Raffaele Ferrari, Jorge H Moreno, et al.
Neurobiology of Aging|February 8, 2014
Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsyRaffaele Ferrari, Mina Ryten, Roberto Simone, et al.
Annals of Neurology|September 20, 2006
Characteristics of frontotemporal dementia patients with a Progranulin mutationEdward D Huey, Jordan Grafman, Eric M Wassermann, et al.
Acta Neuropathologica|March 23, 2011
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS geneJulie S Snowden, Quan Hu, Sara Rollinson, et al.
Neurobiology of Aging|March 31, 2012
Screening for C9ORF72 repeat expansion in FTLDRaffaele Ferrari, Kin Mok, Jorge H Moreno, et al.
Acta Neuropathologica|October 28, 2010
Pathological correlates of frontotemporal lobar degeneration in the elderlyAtik Baborie, Timothy D Griffiths, Evelyn Jaros, et al.
Neuro-Degenerative Diseases|September 7, 2006
Genetic variability in CHMP2B and frontotemporal dementiaParastoo Momeni, Ekaterina Rogaeva, Vivianna Van Deerlin, et al.
Pageof 5