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Elisa Rubino

Showing results (81-90 of 93) with videos related to

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Journal of Alzheimer'S Disease : JAD|May 11, 2016
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 MutationsElkin Luis, Alexandra Ortiz, Luis Eudave, 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.
Journal of Alzheimer'S Disease : JAD|January 13, 2016
PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian PopulationEmanuela Oldoni, Giorgio G Fumagalli, Maria Serpente, 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.
Biological Psychiatry|March 12, 2013
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentationDaniela Galimberti, Chiara Fenoglio, Maria Serpente, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 18, 2023
Mechanical thrombectomy in patients with heart failure: the Italian registry of Endovascular Treatment in Acute StrokeLuana Gentile, Giovanni Pracucci, Valentina Saia, et al.
Brain : a Journal of Neurology|September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersMing Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Neurology|September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Journal of Alzheimer'S Disease : JAD|May 11, 2016
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 MutationsElkin Luis, Alexandra Ortiz, Luis Eudave, 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.
Journal of Alzheimer'S Disease : JAD|January 13, 2016
PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian PopulationEmanuela Oldoni, Giorgio G Fumagalli, Maria Serpente, 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.
Biological Psychiatry|March 12, 2013
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentationDaniela Galimberti, Chiara Fenoglio, Maria Serpente, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 18, 2023
Mechanical thrombectomy in patients with heart failure: the Italian registry of Endovascular Treatment in Acute StrokeLuana Gentile, Giovanni Pracucci, Valentina Saia, et al.
Brain : a Journal of Neurology|September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersMing Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Neurology|September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
Pageof 10