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Journal of Alzheimer'S Disease : JAD
|
April 5, 2018
Findings from the Swedish Study on Familial Alzheimer's Disease Including the APP Swedish Double Mutation
Steinunn Thordardottir, Caroline Graff
Frontiers in Aging Neuroscience
|
October 24, 2022
Practice effects in cognitive assessments three years later in non-carriers but not in symptom-free mutation carriers of autosomal-dominant Alzheimer's disease: Exemplifying procedural learning and memory?
Ove Almkvist, Caroline Graff
Genes
|
December 24, 2021
The <i>APOE</i> ε4 Allele Affects Cognitive Functions Differently in Carriers of <i>APP</i> Mutations Compared to Carriers of <i>PSEN1</i> Mutations in Autosomal-Dominant Alzheimer's Disease
Ove Almkvist, Caroline Graff
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
August 10, 2013
[Alzheimer's disease and genetics]
Arvid Rongve, Dag Årsland, Caroline Graff
Journal of Alzheimer'S Disease : JAD
|
December 31, 2023
Odor Identification Across Time in Mutation Carriers and Non-Carriers in Autosomal-Dominant Alzheimer's Disease
Ove Almkvist, Maria Larsson, Caroline Graff
Best Practice & Research. Clinical Obstetrics & Gynaecology
|
December 12, 2002
Mitochondrial diseases
Caroline Graff, The-Hung Bui, Nils-Göran Larsson
Biological Chemistry
|
June 24, 2003
Synchronization of the molecular clockwork by light- and food-related cues in mammals
Etienne Challet, Ivette Caldelas, Caroline Graff, et al.
Neuropharmacology
|
November 7, 2006
5-HT3 receptor-mediated photic-like responses of the circadian clock in the rat
Caroline Graff, Etienne Challet, Paul Pévet, et al.
Journal of Neurogenetics
|
October 6, 2010
A DNA methylation study of the amyloid precursor protein gene in several brain regions from patients with familial Alzheimer disease
Jesper Brohede, Mia Rinde, Bengt Winblad, et al.
European Journal of Human Genetics : EJHG
|
March 23, 2007
The use of grid computing to drive data-intensive genetic research
Jorge Andrade, Malin Andersen, Anna Sillén, et al.
Page
of 27
Search research articles
Search
Showing results (1-10 of 267) with videos related to
Sort By:
Page
of 27
Journal of Alzheimer'S Disease : JAD
|
April 5, 2018
Findings from the Swedish Study on Familial Alzheimer's Disease Including the APP Swedish Double Mutation
Steinunn Thordardottir, Caroline Graff
Frontiers in Aging Neuroscience
|
October 24, 2022
Practice effects in cognitive assessments three years later in non-carriers but not in symptom-free mutation carriers of autosomal-dominant Alzheimer's disease: Exemplifying procedural learning and memory?
Ove Almkvist, Caroline Graff
Genes
|
December 24, 2021
The <i>APOE</i> ε4 Allele Affects Cognitive Functions Differently in Carriers of <i>APP</i> Mutations Compared to Carriers of <i>PSEN1</i> Mutations in Autosomal-Dominant Alzheimer's Disease
Ove Almkvist, Caroline Graff
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
August 10, 2013
[Alzheimer's disease and genetics]
Arvid Rongve, Dag Årsland, Caroline Graff
Journal of Alzheimer'S Disease : JAD
|
December 31, 2023
Odor Identification Across Time in Mutation Carriers and Non-Carriers in Autosomal-Dominant Alzheimer's Disease
Ove Almkvist, Maria Larsson, Caroline Graff
Best Practice & Research. Clinical Obstetrics & Gynaecology
|
December 12, 2002
Mitochondrial diseases
Caroline Graff, The-Hung Bui, Nils-Göran Larsson
Biological Chemistry
|
June 24, 2003
Synchronization of the molecular clockwork by light- and food-related cues in mammals
Etienne Challet, Ivette Caldelas, Caroline Graff, et al.
Neuropharmacology
|
November 7, 2006
5-HT3 receptor-mediated photic-like responses of the circadian clock in the rat
Caroline Graff, Etienne Challet, Paul Pévet, et al.
Journal of Neurogenetics
|
October 6, 2010
A DNA methylation study of the amyloid precursor protein gene in several brain regions from patients with familial Alzheimer disease
Jesper Brohede, Mia Rinde, Bengt Winblad, et al.
European Journal of Human Genetics : EJHG
|
March 23, 2007
The use of grid computing to drive data-intensive genetic research
Jorge Andrade, Malin Andersen, Anna Sillén, et al.
Page
of 27