Detalhe da pesquisa
1.
TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early-onset autosomal dominant dementia with amyloid load and parkinsonism.
Alzheimers Dement;
19(7): 2805-2815, 2023 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36576960
2.
Behavioral Evolution of Progressive Semantic Aphasia in Comparison with Nonfluent Aphasia.
Dement Geriatr Cogn Disord;
41(1-2): 1-8, 2016.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26426392
3.
Familial benign frontotemporal deterioration with C9ORF72 hexanucleotide expansion.
Alzheimers Dement;
10(5 Suppl): S284-9, 2014 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24439166
4.
A systematic review of progranulin concentrations in biofluids in over 7,000 people-assessing the pathogenicity of GRN mutations and other influencing factors.
Alzheimers Res Ther;
16(1): 66, 2024 Mar 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38539243
5.
Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation.
J Neurol Neurosurg Psychiatry;
88(11): 996-997, 2017 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28365590
6.
Outcome of mild cognitive impairment comparing early memory profiles.
Am J Geriatr Psychiatry;
20(10): 827-35, 2012 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21934475
7.
Visual hallucinations and HLA class II antigens in cortical dementia.
Dement Geriatr Cogn Disord;
30(1): 8-11, 2010.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20606439
8.
Variability of age at onset in siblings with familial Alzheimer disease.
Arch Neurol;
64(12): 1743-8, 2007 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18071037
9.
Clinical-genetic correlations in familial Alzheimer's disease caused by presenilin 1 mutations.
J Alzheimers Dis;
19(3): 873-84, 2010.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20157243