scholarly journals Correlating familial Alzheimer’s disease gene mutations with clinical phenotype

2010 ◽  
Vol 4 (1) ◽  
pp. 99-112 ◽  
Author(s):  
Natalie S Ryan ◽  
Martin N Rossor
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Disease Gene ◽  
Clinical Phenotype ◽  
Gene Mutations ◽  
Familial Alzheimer’S Disease ◽  
Familial Alzheimer's Disease

The Effects of Gene Mutations on Default Mode Network in Familial Alzheimer’s Disease

2017 ◽  
Vol 56 (1) ◽  
pp. 327-334 ◽  
Author(s):  
Xiaozhen Li ◽  
Eric Westman ◽  
Steinunn Thordardottir ◽  
Anne Kinhult Ståhlbom ◽  
Ove Almkvist ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Default Mode Network ◽  
Gene Mutations ◽  
Familial Alzheimer’S Disease ◽  
Default Mode ◽  
Familial Alzheimer's Disease

scholarly journals IC-O1-02: Are early atrophy patterns in autosomal dominant familial Alzheimer's disease gene-dependent?

2013 ◽  
Vol 9 ◽  
pp. P3-P4
Author(s):  
Kirsi Kinnunen ◽  
Natalie Ryan ◽  
David Cash ◽  
António Bastos Leite ◽  
Sarah Finnegan ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Autosomal Dominant ◽  
Disease Gene ◽  
Familial Alzheimer’S Disease ◽  
Familial Alzheimer's Disease

scholarly journals Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series

2016 ◽  
Vol 15 (13) ◽  
pp. 1326-1335 ◽  
Author(s):  
Natalie S Ryan ◽  
Jennifer M Nicholas ◽  
Philip S J Weston ◽  
Yuying Liang ◽  
Tammaryn Lashley ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Autosomal Dominant ◽  
Clinical Phenotype ◽  
Case Series ◽  
Genetic Associations ◽  
Familial Alzheimer’S Disease ◽  
Familial Alzheimer's Disease

P1-269: Are early atrophy patterns in autosomal dominant familial Alzheimer's disease gene-dependent?

2013 ◽  
Vol 9 ◽  
pp. P251-P252 ◽  
Author(s):  
Kirsi Kinnunen ◽  
Natalie Ryan ◽  
David Cash ◽  
António Bastos Leite ◽  
Sarah Finnegan ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Autosomal Dominant ◽  
Disease Gene ◽  
Familial Alzheimer’S Disease ◽  
Familial Alzheimer's Disease

P3-224: Clinical phenotype of familial Alzheimer's disease caused by the H163R presenilin 1 mutation

2008 ◽  
Vol 4 ◽  
pp. T586-T586
Author(s):  
Estrella Gómez-Tortosa ◽  
Sagrario Manzano ◽  
David G. Muñoz ◽  
M. José Sainz ◽  
Adolfo Jiménez-Huete ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Clinical Phenotype ◽  
Presenilin 1 ◽  
Familial Alzheimer’S Disease ◽  
Presenilin 1 Mutation ◽  
Familial Alzheimer's Disease

Alteration of acylphosphatase levels in familial Alzheimer's disease fibroblasts with presenilin gene mutations

1996 ◽  
Vol 210 (3) ◽  
pp. 153-156 ◽  
Author(s):  
Gianfranco Liguri ◽  
Cristina Cecchi ◽  
Stefania Latorraca ◽  
Alessandro Pieri ◽  
Sandro Sorbi ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Gene Mutations ◽  
Familial Alzheimer’S Disease ◽  
Familial Alzheimer's Disease
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