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Adeline Rollin-Sillaire

Showing results (11-20 of 24) with videos related to

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Journal of Neuroradiology = Journal De Neuroradiologie|July 4, 2025
BrainAGE latent representation clustering is associated with longitudinal disease progression in early-onset Alzheimer's diseaseDorian Manouvriez, Grégory Kuchcinski, Vincent Roca, et al.
European Radiology|July 26, 2022
Quantitative susceptibility mapping demonstrates different patterns of iron overload in subtypes of early-onset Alzheimer's diseaseGrégory Kuchcinski, Lucas Patin, Renaud Lopes, et al.
Alzheimer'S Research & Therapy|January 9, 2021
Characteristics and progression of patients with frontotemporal dementia in a regional memory clinic networkMélanie Leroy, Maxime Bertoux, Emilie Skrobala, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer diseaseAnne Rovelet-Lecrux, Solenn Legallic, David Wallon, et al.
Alzheimer'S Research & Therapy|May 7, 2025
Soluble SorLA in CSF, a novel biomarker to explore disrupted trafficking of SorLA protein in Alzheimer diseaseRomain Castelot, Aline Zarea, David Wallon, et al.
Neurology|July 29, 2016
Seizures in dominantly inherited Alzheimer diseaseAline Zarea, Camille Charbonnier, Anne Rovelet-Lecrux, et al.
Journal of Alzheimer'S Disease : JAD|April 6, 2012
The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkersDavid Wallon, Stéphane Rousseau, Anne Rovelet-Lecrux, et al.
Neurology|April 3, 2016
ABCA7 rare variants and Alzheimer disease riskKilan Le Guennec, Gaël Nicolas, Olivier Quenez, et al.
Neurobiology of Aging|August 10, 2017
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controlsCéline Bellenguez, Camille Charbonnier, Benjamin Grenier-Boley, et al.
Journal of Alzheimer'S Disease : JAD|August 6, 2019
Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 YearsMorgane Lacour, Olivier Quenez, Anne Rovelet-Lecrux, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Journal of Neuroradiology = Journal De Neuroradiologie|July 4, 2025
BrainAGE latent representation clustering is associated with longitudinal disease progression in early-onset Alzheimer's diseaseDorian Manouvriez, Grégory Kuchcinski, Vincent Roca, et al.
European Radiology|July 26, 2022
Quantitative susceptibility mapping demonstrates different patterns of iron overload in subtypes of early-onset Alzheimer's diseaseGrégory Kuchcinski, Lucas Patin, Renaud Lopes, et al.
Alzheimer'S Research & Therapy|January 9, 2021
Characteristics and progression of patients with frontotemporal dementia in a regional memory clinic networkMélanie Leroy, Maxime Bertoux, Emilie Skrobala, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer diseaseAnne Rovelet-Lecrux, Solenn Legallic, David Wallon, et al.
Alzheimer'S Research & Therapy|May 7, 2025
Soluble SorLA in CSF, a novel biomarker to explore disrupted trafficking of SorLA protein in Alzheimer diseaseRomain Castelot, Aline Zarea, David Wallon, et al.
Neurology|July 29, 2016
Seizures in dominantly inherited Alzheimer diseaseAline Zarea, Camille Charbonnier, Anne Rovelet-Lecrux, et al.
Journal of Alzheimer'S Disease : JAD|April 6, 2012
The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkersDavid Wallon, Stéphane Rousseau, Anne Rovelet-Lecrux, et al.
Neurology|April 3, 2016
ABCA7 rare variants and Alzheimer disease riskKilan Le Guennec, Gaël Nicolas, Olivier Quenez, et al.
Neurobiology of Aging|August 10, 2017
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controlsCéline Bellenguez, Camille Charbonnier, Benjamin Grenier-Boley, et al.
Journal of Alzheimer'S Disease : JAD|August 6, 2019
Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 YearsMorgane Lacour, Olivier Quenez, Anne Rovelet-Lecrux, et al.
Pageof 3