P4-123: Clinical phenotype of Alzheimer's disease caused by presenilin 1 mutations in Spain

2009 ◽  
Vol 5 (4S_Part_15) ◽  
pp. P467-P468
Author(s):  
Estrella Gómez-Tortosa ◽  
M. Sagrario Barquero ◽  
Fernando Castellanos ◽  
Martín Zurdo ◽  
Eulogio Gil-Necija ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Clinical Phenotype ◽  
Presenilin 1

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

Clinical Phenotype of G206D Mutation in the Presenilin 1 Gene in Pathologically Confirmed Familial Alzheimer's Disease

2011 ◽  
Vol 25 (1) ◽  
pp. 145-150 ◽  
Author(s):  
Ya-Ying Wu ◽  
Irene Han-Juo Cheng ◽  
Chin-Cheng Lee ◽  
Ming-Jang Chiu ◽  
Ming-Jen Lee ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Clinical Phenotype ◽  
Presenilin 1 ◽  
Familial Alzheimer’S Disease ◽  
Familial Alzheimer's Disease

Depressive Symptoms and APOE ε2 Broad the Natural History in Presenilin-1 E280A Familial Early-Onset Alzheimer's Disease

2018 ◽  
Author(s):  
Natalia Acosta-Baena ◽  
Carlos Mario Lopera-Gómez ◽  
Mario César Jaramillo-Elorza ◽  
Margarita Giraldo-Chica ◽  
Mauricio Arcos-Burgos ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Depressive Symptoms ◽  
Natural History ◽  
Early Onset ◽  
Presenilin 1 ◽  
Early Onset Alzheimer’S Disease

A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease

2010 ◽  
Vol 468 (1) ◽  
pp. 34-37 ◽  
Author(s):  
Jifeng Guo ◽  
Jiaohua Wei ◽  
Shusheng Liao ◽  
Lei Wang ◽  
Hong Jiang ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Early Onset ◽  
Presenilin 1 ◽  
Chinese Family ◽  
Presenilin 1 Mutation ◽  
Early Onset Alzheimer’S Disease

Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer’s disease

2016 ◽  
Vol 610 ◽  
pp. 150-153 ◽  
Author(s):  
Andrea Tedde ◽  
Antonella Bartoli ◽  
Irene Piaceri ◽  
Sara Ferrara ◽  
Silvia Bagnoli ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Late Onset ◽  
Presenilin 1 ◽  
Italian Family ◽  
Presenilin 1 Mutation

scholarly journals The Role of Presenilin-1 in the γ-Secretase Cleavage of the Amyloid Precursor Protein of Alzheimer's Disease

2000 ◽  
Vol 275 (3) ◽  
pp. 1525-1528 ◽  
Author(s):  
Jean-Noël Octave ◽  
Rachid Essalmani ◽  
Bernadette Tasiaux ◽  
Jean Menager ◽  
Christian Czech ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Amyloid Precursor Protein ◽  
Precursor Protein ◽  
Presenilin 1

Presenilin-1 Polymorphism in Alzheimer's Disease and Vascular Dementia

1997 ◽  
Vol 146 (2) ◽  
pp. 567-569 ◽  
Author(s):  
Sachio Matsushita ◽  
Hiroyuki Arai ◽  
Taro Muramatsu ◽  
Kiyoko Makimoto ◽  
Takuma Nakagawa ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Vascular Dementia ◽  
Presenilin 1

Neurotoxic mechanisms triggered by Alzheimer's disease-linked mutant M146L presenilin 1: involvement of NO synthase via a novel pertussis toxin target

2002 ◽  
Vol 80 (3) ◽  
pp. 426-437 ◽  
Author(s):  
Yuichi Hashimoto ◽  
Yuko Ito ◽  
Erika Arakawa ◽  
Yoshiko Kita ◽  
Kenzo Terashita ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Pertussis Toxin ◽  
No Synthase ◽  
Presenilin 1
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