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G Maletta

Showing results (11-20 of 19) with videos related to

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Neurobiology of Aging|May 21, 2005
The effects of APOE and tau gene variability on risk of frontotemporal dementiaL Bernardi, R G Maletta, C Tomaino, et al.
Human Molecular Genetics|June 9, 2014
Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patientsZhengrui Xi, Innocenzo Rainero, Elisa Rubino, et al.
Neurology|May 8, 2015
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease familyMaria E Conidi, Livia Bernardi, Gianfranco Puccio, et al.
Neurology|July 11, 2007
Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutationA C Bruni, P Momeni, L Bernardi, et al.
Acta Neuropathologica|February 27, 2015
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patientsZhengrui Xi, Ming Zhang, Amalia C Bruni, et al.
Brain : a Journal of Neurology|April 3, 2015
Mutation analysis of CHCHD10 in different neurodegenerative diseasesMing Zhang, Zhengrui Xi, Lorne Zinman, et al.
Journal of Alzheimer'S Disease : JAD|January 28, 2017
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal DementiaRaffaele Ferrari, Mario Grassi, Francesca Graziano, et al.
Neurobiology of Aging|July 9, 2015
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementiaRaffaele Ferrari, Mario Grassi, Erika Salvi, et al.
Archives of Neurology|September 12, 2012
Investigation of c9orf72 in 4 neurodegenerative disordersZhengrui Xi, Lorne Zinman, Yakov Grinberg, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Neurobiology of Aging|May 21, 2005
The effects of APOE and tau gene variability on risk of frontotemporal dementiaL Bernardi, R G Maletta, C Tomaino, et al.
Human Molecular Genetics|June 9, 2014
Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patientsZhengrui Xi, Innocenzo Rainero, Elisa Rubino, et al.
Neurology|May 8, 2015
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease familyMaria E Conidi, Livia Bernardi, Gianfranco Puccio, et al.
Neurology|July 11, 2007
Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutationA C Bruni, P Momeni, L Bernardi, et al.
Acta Neuropathologica|February 27, 2015
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patientsZhengrui Xi, Ming Zhang, Amalia C Bruni, et al.
Brain : a Journal of Neurology|April 3, 2015
Mutation analysis of CHCHD10 in different neurodegenerative diseasesMing Zhang, Zhengrui Xi, Lorne Zinman, et al.
Journal of Alzheimer'S Disease : JAD|January 28, 2017
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal DementiaRaffaele Ferrari, Mario Grassi, Francesca Graziano, et al.
Neurobiology of Aging|July 9, 2015
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementiaRaffaele Ferrari, Mario Grassi, Erika Salvi, et al.
Archives of Neurology|September 12, 2012
Investigation of c9orf72 in 4 neurodegenerative disordersZhengrui Xi, Lorne Zinman, Yakov Grinberg, et al.
Pageof 2