Detalhe da pesquisa
1.
Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study.
Hum Mol Genet
; 22(21): 4349-56, 2013 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23773996
2.
Rare variants in LRRK1 and Parkinson's disease.
Neurogenetics
; 15(1): 49-57, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24241507
3.
Amyloid-ß contributes to blood-brain barrier leakage in transgenic human amyloid precursor protein mice and in humans with cerebral amyloid angiopathy.
Stroke
; 43(2): 514-23, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22116809
4.
Differential impact of ApoE ε4 on cortical activation during famous face recognition in cognitively intact individuals and patients with amnestic mild cognitive impairment.
Alzheimer Dis Assoc Disord
; 25(3): 250-61, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21192235
5.
Structural and functional neural correlates of visuospatial information processing in normal aging and amnestic mild cognitive impairment.
Neurobiol Aging
; 33(12): 2782-97, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22429887
6.
Monocyte cholesterol homeostasis correlates with the presence of detergent resistant membrane microdomains.
Cytometry A
; 71(7): 486-94, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17458880
7.
Characterization of the kindred of Alois Alzheimer's patient with plaque-only dementia.
Alzheimer Dis Assoc Disord
; 20(4): 291-4, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-17132975
8.
[Familial plaque-only Alzheimer's disease in the Rottal-Inn and Passau counties]. / Familiäre Plaque-only-Alzheimer-Krankheit in den Landkreisen Rottal-Inn und Passau--Genetisch-genealogische Alzheimer-Forschung.
Psychiatr Prax
; 31 Suppl 1: S61-3, 2004 Nov.
Artigo
em Alemão
| MEDLINE | ID: mdl-15570504
9.
Alzheimer's second patient: Johann F. and his family.
Ann Neurol
; 52(4): 520-3, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12325085
10.
Novel PS1 mutation in a Bavarian kindred with familial Alzheimer disease.
Alzheimer Dis Assoc Disord
; 18(4): 256-8, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15592140
11.
Frontal lobe atrophy due to a mutation in the cholesterol binding protein HE1/NPC2.
Ann Neurol
; 52(6): 743-9, 2002 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-12447927