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Albert Llado

Showing results (1-10 of 7) with videos related to

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Annals of Neurology|June 25, 2013
Low cerebrospinal fluid concentration of mitochondrial DNA in preclinical Alzheimer diseasePetar Podlesniy, Joana Figueiro-Silva, Albert Llado, et al.
Annals of Neurology|January 17, 2014
Reply: To PMID 23794434Petar Podlesniy, Joana Figueiro-Silva, Albert Llado, et al.
Neurology|November 11, 2024
Association of Initial Side of Brain Atrophy With Clinical Features and Disease Progression in Patients With <i>GRN</i> Frontotemporal DementiaSergi Borrego-Ecija, Jordi Juncà-Parella, Marijne Vandebergh, et al.
Human Mutation|December 24, 2016
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral SclerosisJulie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Human Mutation|November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeatsJulie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Acta Neuropathologica|June 6, 2014
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationJulie van der Zee, Tim Van Langenhove, Gabor G Kovacs, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Annals of Neurology|June 25, 2013
Low cerebrospinal fluid concentration of mitochondrial DNA in preclinical Alzheimer diseasePetar Podlesniy, Joana Figueiro-Silva, Albert Llado, et al.
Annals of Neurology|January 17, 2014
Reply: To PMID 23794434Petar Podlesniy, Joana Figueiro-Silva, Albert Llado, et al.
Neurology|November 11, 2024
Association of Initial Side of Brain Atrophy With Clinical Features and Disease Progression in Patients With <i>GRN</i> Frontotemporal DementiaSergi Borrego-Ecija, Jordi Juncà-Parella, Marijne Vandebergh, et al.
Human Mutation|December 24, 2016
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral SclerosisJulie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Human Mutation|November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeatsJulie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Acta Neuropathologica|June 6, 2014
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationJulie van der Zee, Tim Van Langenhove, Gabor G Kovacs, et al.
Pageof 1